
Inflammation and oxidative stress are implicated in several chronic disorders, while healthy foods and especially fermented beverages and those containing probiotics can provide anti-inflammatory and antioxidant protection against such manifestations and the associated disorders. Water kefir is such a beverage that is rich in both probiotic microbiota and anti-inflammatory bioactives, with an increasing demand as an alternative to a fermented product based on non-dairy matrix with potential health properties. Within this study, the health-promoting properties of the most representative species and strains of microorganisms present in water kefir grains, as well as the health benefits attributed to the bioactive metabolites produced by each individual strain in a series of their cultures, were thoroughly reviewed. Emphasis was given to the antioxidant, antithrombotic, and anti-inflammatory bio-functionalities of both the cultured microorganisms and the bioactive metabolites produced in each case. Moreover, an extensive presentation of the antioxidant and anti-inflammatory health benefits observed from the overall water kefir cultures and classic water kefir beverages obtained were also conducted. Finally, the use of water kefir for the production of several other bio-functional products, including fermented functional foods, supplements, nutraceuticals, nutricosmetics, cosmeceuticals, and cosmetic applications with anti-inflammatory and antioxidant health promoting potential was also thoroughly discussed. Limitations and future perspectives on the use of water kefir, its microorganisms, and their bioactive metabolites are also outlined.
Citation: Dimitra Papadopoulou, Vasiliki Chrysikopoulou, Aikaterini Rampaouni, Alexandros Tsoupras. Antioxidant and anti-inflammatory properties of water kefir microbiota and its bioactive metabolites for health promoting bio-functional products and applications[J]. AIMS Microbiology, 2024, 10(4): 756-811. doi: 10.3934/microbiol.2024034
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Inflammation and oxidative stress are implicated in several chronic disorders, while healthy foods and especially fermented beverages and those containing probiotics can provide anti-inflammatory and antioxidant protection against such manifestations and the associated disorders. Water kefir is such a beverage that is rich in both probiotic microbiota and anti-inflammatory bioactives, with an increasing demand as an alternative to a fermented product based on non-dairy matrix with potential health properties. Within this study, the health-promoting properties of the most representative species and strains of microorganisms present in water kefir grains, as well as the health benefits attributed to the bioactive metabolites produced by each individual strain in a series of their cultures, were thoroughly reviewed. Emphasis was given to the antioxidant, antithrombotic, and anti-inflammatory bio-functionalities of both the cultured microorganisms and the bioactive metabolites produced in each case. Moreover, an extensive presentation of the antioxidant and anti-inflammatory health benefits observed from the overall water kefir cultures and classic water kefir beverages obtained were also conducted. Finally, the use of water kefir for the production of several other bio-functional products, including fermented functional foods, supplements, nutraceuticals, nutricosmetics, cosmeceuticals, and cosmetic applications with anti-inflammatory and antioxidant health promoting potential was also thoroughly discussed. Limitations and future perspectives on the use of water kefir, its microorganisms, and their bioactive metabolites are also outlined.
Fetal cardiac monitoring in late pregnancy is mainly based on the analysis of changes in the fetal heart rate (fHR) [1,2] to determine whether the fetus is responsive to various physiological stimuli [1,2,3]. Finer studies of the variability of the fetal heart rate have demonstrated how this parameter relates to fetal development [4] and can be used to assess the proper functioning of the autonomic nervous system [5]. Ultrasound-based devices such as the cardiotocograph have been the primary choice for this purpose [6], whereas cardiac echocardiography is adopted for the assessment of fetal heart diseases [7]. In this context, fetal electrocardiography (fECG) enables access to very relevant information on fetal cardiac function, based on the electrical activation pattern of the fetal heart [6]. However, invasive techniques for this purpose, which record the fECG using a spiral scalp electrode, can only be used intrapartum, when membranes have already broken [2]. These techniques produce a signal of acceptable quality so they are currently adopted in clinical practice [8], even though they cannot be exploited for diagnostic purposes in early pregnancy, when in-utero treatments or birth scheduling can be considered [9]. Conversely, non-invasive fetal ECG (fECG) can be performed using a relatively comfortable and safe procedure at different gestational ages by applying surface electrodes to the maternal abdomen. However, the signal-to-noise ratio (SNR) for this procedure is low, due to the small size of the fetal heart, the feto-maternal compartments [10], maternal physiological interference, and instrumental noise [11]. Furthermore, fECG extraction from the interfering maternal ECG (mECG) is hampered by their spectral overlap so that, despite research efforts and the first devices having been introduced to the market, extracting a qualitatively effective non-invasive fECG remains an open research issue.
Several techniques for extracting the fECG from non-invasive recordings have been investigated in recent decades, including adaptive filtering, methods based on the wavelet transform, independent component analysis, principle component analysis, and soft computing tools like adaptive neural networks, genetic algorithms, and adaptive neuro-fuzzy inference systems [11]. Despite the superior performance demonstrated by blind-source separation techniques over that of adaptive filters for this specific problem [12], the latter can overcome the intrinsic limitations of the former, which requires a large number of channels (greater than eight, overall [13]). Considering reducing the number of electrodes applied on the maternal body is one of the constraints of this specific application, especially when required for unobtrusive wearable systems, adaptive filters can still be considered to be a valuable technique. Moreover, they can be naturally implemented in real time, which is not the case for several excellent blind-source separation methods, with some exceptions (e.g., [14,15]). Among the methods proposed in the literature, adaptive filters have been proposed by several authors who utilize different algorithms [16,17,18,19,20,21,22]. Originally, this approach was introduced by the authors of [16], whereby the adaptive filter received four chest ECG inputs to cancel the maternal component from a single abdominal lead. More recently, an adaptive filtering approach was proposed in the 2013 Physionet/Computing in Cardiology Challenge [23], wherein the dataset included only four abdominal channels per record. In [24], the authors cancelled the mECG from the recordings of four abdominal leads using an adaptive filter that received as references three out of four channels. The filter output was then subtracted from the channel and the filter coefficients were optimized to minimize the sum of the squares of this difference. A Wiener-filter-like method was then adopted to compute the filter coefficients. Behar et al. [20] compared an echo-state neural-network-based filtering approach to a least mean square filter, recursive least square (RLS) adaptive filter, and template subtraction techniques. The first performed slightly better than the others but the improvement was not statistically significant. Non-invasive fECG extraction has also been investigated by combining methods, for example, using multi-stage adaptive filters [21] or adaptive filters and wavelet transform [25].
The drawback of adaptive filtering using a reduced number of leads (in principle one thoracic and one abdominal) is the strong dependency of the output quality on the electrode placement, since the reference mECG lead must be morphologically similar to the mECG projection contaminating the fECG in the abdominal leads. This problem could be solved by using multiple non-coplanar thoracic leads to roughly reconstruct the mECG morphology in any abdominal lead. The multi-reference approach has been investigated using different adaptive filtering methods [22] but there has yet to be an in-depth methodological analysis that can answer the following important questions: Is it worthwhile to use multiple mECG reference leads rather than a single lead when dealing with real non-invasive fECG recordings? Or, alternatively, to what extent can a single-reference adaptive filter provide adequate mECG attenuation, at least on abdominal leads parallel to the reference lead? When only the fHR is needed, is it effective to adopt the single-reference approach? The answer to these questions is relevant for guiding the selection of the appropriate technique for a given problem.
To answer the above questions, in this work, we analyzed the performance of a prototypical multi-reference (MR) adaptive filter, i.e., QR decomposition with back-substitution recursive least-squares (QRD-RLS), which we chose for its numerical stability and good performance. Its performance was compared to its single-reference (SR) variant by cancelling the mECG on abdominal leads having different spatial orientations. The assessment was performed on a large dataset comprising real recordings acquired on 20 pregnant women within the framework of the non-invasive fetal ECG analysis (NInFEA) project of the University of Cagliari, and on synthetic signals generated by the FECGSYN toolbox [26]. The real dataset contained a total of 112 non-invasive fECG signal channels, and the synthetic dataset contained a total of 400 channels. These datasets enabled an in-depth analysis of the results, which were found to subvert some common-sense beliefs regarding the use of SR adaptive filters in this specific application.
To perform some of the analyses required for comparing the SR and MR QRD-RLS adaptive filters, we used a custom dataset. This was necessary because of the lack of available datasets featuring the required representative leads. In this section, we describe the real and synthetic datasets used in the performance analysis.
The real dataset is composed of biopotentials acquired from healthy pregnant women. Along with the electrophysiological signals, a simultaneous cardiac pulsed-wave doppler (PWD) trace was recorded. In this work, this dataset played the main role in providing ground truth for the fetal heart activity from a mechanical perspective, which was important for confirming the presence of fetal QRS complexes. The PWD traces were acquired using a Philips iE33 Ultrasound Machine (Philips, The Netherlands), as described in [27]. The biopotentials were recorded with a Porti7 portable physiological measurement system (TMSi, The Netherlands) at 2048 Hz and 22–bit resolution. No high-pass filtering was performed, and the actual bandwidth was limited by a digital decimation filter with a cut-off frequency of approximately 550 Hz. Bipolar channels, which were used on the thorax, enabled differential measurements, whereas unipolar channels connected to electrodes placed on the abdomen measured the biopotential of one electrode with respect to the average of all the unipolar electrodes in use. Figure 1 shows the positions of the electrodes on the maternal body.
The chosen configuration included six electrodes for three bipolar channels that captured three non-coplanar maternal leads on the chest and three abdominal electrodes to obtain three digital abdominal bipolar leads and one unipolar lead. A ground electrode was placed on the right hip. Figure 2 shows a sample trace acquired using this setup.
Figure 3 shows an example of the simultaneous recording of PWD traces and electrophysiological signals. The specific heart projection adopted for this dataset for ultrasound recording was the five-chamber apical window, which allows inspection of the flows across the mitral and aortic valves.
The dataset included 28 multichannel signals from 20 healthy pregnant women between the 21st and the 27th weeks of gestation with healthy fetuses (for a total of 112 abdominal channels leading to as many non-invasive fECG signals). The gestational epoch was selected to ensure the best morphological accuracy of the transabdominal signals and to limit the influence of the vernix caseosa, which is characterized by the lowest conductivity of the anatomical layers surrounding the fetus [10]. The signal duration was fixed to ten seconds, similar to the standard resting ECG. Recording was performed at the Division of Pediatric Cardiology of the S. Michele Hospital (Cagliari, Italy). The study was approved by the Independent Ethical Committee of the Cagliari University Hospital (AOU Cagliari) and was performed according to the principles outlined in the Helsinki Declaration of 1975, as revised in 2000. All the volunteers provided their signed informed consent to the protocol.
The FECGSYN tool [26,28] is a reference open-source platform for non-invasive fetal electrocardiography research1. In abdominal fECG recordings, surface electrodes measure the electrical potential created by cardiac sources (i.e., maternal and fetal myocardia) and noise sources (e.g., muscle activity from movement or contractions), which propagate throughout the volume conductor. The FECGSYN simulator considers all of these potentials to be point dipoles that can be rotated and translated. These dipoles have two basic attributes: a vector represented by three coordinates in the Cartesian coordinate system and a location, which, together with the electrode locations, defines a matrix of the signals propagated to the observation points. To project the ECG signals, we used a projection matrix built using the cardiac dipole model. This projection matrix contains information about the permittivity of the conductor (assumed constant), dipole origin, and relative location between the observing electrodes and the source [28].
1 Available at http://fernandoandreotti.github.io/fecgsyn/
By exploiting this principle, FECGSYN is able to generate maternal–fetal ECG mixtures with a realistic amplitude, morphology, beat-to-beat variability, and heart rate changes and noise [26]. Movements (rotations and translations) of fetal and maternal hearts due to respiration, fetal activity, and uterine contractions can also be considered by the simulator. In this work, the fECG mixtures were generated at 2048 Hz with a duration of 10 s. To the clean signals, we added realistic motion artifacts, electrode movements, and baseline wandering. The electrodes were placed as shown in Figure 4, which was also the reference position for the real recordings. Figure 5 shows an example of the synthetic signals generated specifically for this purpose.
The cardiac and noise signals were calibrated with respect to the maternal signal, for which we chose the SNR of the fECG relative to the mECG (SNRfm), i.e., –18 dB, and the SNR of the mECG relative to noise (SNRmn). We reproduced five SNRmn values (3 dB, 5 dB, 9 dB, 12 dB, and 15 dB). The maternal and fetal HRs were assumed to be fixed at 90 bpm and 150 bpm, respectively. For each SNRmn, we simulated 20 slightly different fetal heart positions. As such, one hundred virtual subjects were created, each of which included four abdominal signals (Figure 4), i.e., the horizontal (1–2), vertical (1–3), and oblique (1–4) leads and a unipolar channel (4), for a total of four hundred synthetic abdominal signals. For each of these, we also created three non-coplanar thoracic leads (5–6, 5–7, and 7–8).
Generally speaking, an adaptive filter is a self-modifying digital filter that adjusts its coefficients to minimize the error function, which is the distance between the reference signal and the output of the adaptive filter [29]. The adaptive filter can be used in different configurations, one of which is the adaptive noise canceler, whose block diagram is presented in Figure 6, which we adapted to the non-invasive fECG extraction problem. Generally speaking, it is used to extract a clean version of the signal of interest s(k), which is characterized by an additive noise component n(k). The reference signal must be strongly correlated with n(k) but not s(k). The adaptive filter adjusts its coefficients to obtain an output y(k) that approximates n(k), thereby forcing the error signal e(k) to resemble s(k). The adaptation of the filter coefficients follows the minimization process of a particular cost function. With reference to Figure 6, where d(k) is the recorded abdominal signal, x(k) is the reference maternal lead, y(k) is the maternal component of the abdominal signal reconstructed by the filter, and e(k) is the extracted fECG.
d(k)=s(k)+n(k) | (1) |
x(k)≅n(k) | (2) |
y(k)=wTx(k) | (3) |
e(k)≅s(k) | (4) |
From the equations above, we can better understand the effect of the adaptive noise canceler when applied to the fECG extraction problem. The d(k) signal is a combination of the noise and the signal of interest. The maternal lead x(k) approximates the noise, and y(k) is the filter output that has been optimized to mimic the maternal component obtained by the abdominal lead by the use of reference signal x(k). Finally, e(k) is our signal of interest. Compared to other methods, RLS adaptive filters pay for their faster convergence with a higher computational complexity. Moreover, their direct matrix inversion operations may cause numerical stability problems. To address this problem, QRD-RLS filters have been introduced [30], which exhibit both fast convergence and numerical stability. For this reason, we chose the QRD-RLS adaptive filter as the prototypical adaptive filter for this study.
The RLS filter family uses the weighted least-squares objective function, which is defined as follows:
ξD(k)=∑ki=0λk−1[d(i)−wTx(i)]2=eT(k)e(k) | (5) |
In this equation, e(k) is defined as follows:
e(k)=[d(k)λ1/2d(k−1)⋮λk/2d(0)]−[xTPλ1/2xTP(k−1)⋮λk/2xTP(0)]wP(k)=d(k)−xP(k)wP(k) | (6) |
xTP(k)=[xTkxTk−1…xTk−N+1] | (7) |
and N is the number of filter coefficients. The forgetting factor λ, which ranges from 0 to 1, allows the most recent error samples to be emphasized. If we define the R and p parameters, introducing the forgetting factor λ:
R(k)=∑ki=0λk−1x(i)xT(i)=XT(k)X(k) | (8) |
p(k)=∑ki=0λk−1d(i)x(i)=XT(k)d(k) | (9) |
then the optimum solution takes the following form:
w(k)=R−1(k)[x(k)e(k)+R(k)w(k−1)] | (10) |
where the computation of the inverse matrix of R can lead to an ill-conditioned problem. The convergence rate, misalignment, and numerical stability of adaptive algorithms depend on the condition number of the input signal covariance matrix. The higher is this condition number, the slower is the convergence rate and/or the more unstable is the algorithm.
An alternative RLS implementation is based on QR decomposition, which involves the triangularization of the input data matrix. QR decomposition is numerically stable and solves the instability problem of the RLS implementation. We note that matrix X(k) is (k+1)×(N+1), which means that its order increases as the iterations progress. The QR-decomposition process applies an orthogonal matrix Q(k) of order (k+1)×(k+1) to transform X(k) into a triangular matrix U(k) of order (N +1)×(N+1) such that:
Q(k)X(k)=[OU(k)] | (11) |
where O is a null matrix of order (k−N)×(N+1). Matrix Q(k) indicates the overall triangularization process and may be implemented in different ways, such as the numerically well-conditioned Givens rotations or the Householder transformation [31]. The vector eq(k) is expressed as follows:
eq(k)=QP(k)e(k)=[eq1(k)eq2(k)]=[dq1(k)dq2(k)]−[0UP(k)]wP(k) | (12) |
Minimizing ‖eq(k)‖2 or the cost function ξD(k) is equivalent. Therefore, Eq. (5) is minimized by choosing the wP(k) in Eq (12) such that dq2(k)−UP(k)wP(k)=0 [31].
The theory presented thus far was conceived for the SR implementation of the QRD-RLS adaptive filter. In a MR implementation, there are multiple reference signals that meet the definition of noise (Figure 7). If M is the number of channels, which in our case is equal to three, i.e., the number of non-coplanar bipolar thoracic leads (x1, x2, and x3 in Figure 7), N1, N2, …, NM is the number of taps for each of the M filters. In our approach, in a sample, we shift from each channel one at a time and progress recursively from the first to last channel. In this work, we implemented the filtering routines provided in [31] and adapted them to this problem.
For the specific application, we chose the first thoracic lead (1 m in Figure 1 for the real dataset and 5–6 in Figure 4 for the synthetic one), which is perpendicular to the sagittal plane, to be the input reference for the SR technique, whereas we used all three thoracic leads (1 m, 2 m, and 3 m in Figure 1 for the real dataset and 5–6, 5–7, and 7–8 in Figure 4 for the synthetic one) for the MR version. Moreover, adaptive filters require proper tuning of their parameters to achieve the best compromise between performance and computational cost [20]. In the RLS implementation, there are two important parameters: the forgetting factor λ and the number of taps N. In both implementations, we set λ to 0.999 and N to 20 (for each of the three channels in the MR implementation). We optimized both these parameters in the training phase on the real dataset. We note that other studies have obtained the same values following similar procedures [20].
Baseline wandering, especially when no high-pass filtering occurs in the analog signal acquisition chain, cannot be addressed by the adaptive filter in the real dataset. In fact, several factors contribute to its generation, from maternal breathing to fetal and cable movements, which have different reflections on different leads, even more so on the abdominal leads. To address this, a simple pre-processing step is usually recommended prior to fECG extraction. As proved in [20], the cut-off frequency of the high-pass filter should be higher than that imposed by the current guidelines, which is 0.67 Hz [32], mainly to compensate for such a stronger baseline wandering. To preserve the low-frequency components of the ECG, which are mainly related to P and T and to the ST segments, the signal was high-pass filtered only at 1 Hz by a bidirectional implementation of an equiripple finite impulse response (FIR) filter of 1124–th order.
In principle, the availability of three non-coplanar leads for the mECG should enable projection of the maternal heart vector in any lead direction. Obviously, by providing more information for the maternal heart vector than is possible with a single projection in a given direction, the MR QRD-RLS filter should outperform its SR counterpart. However, a proper selection of the abdominal lead parallel to the maternal chest lead used as reference could be expected to produce acceptable results, at least with respect to the fHR computation. Since a reduction in the number of processing leads is important in the context of this application, especially for wearable monitoring systems, this assumption must be carefully verified. For instance, currently available wearable non-invasive fECG monitors, such as the Monica Novii Wireless Patch System (Monica Healthcare, Nottingham, UK) and Nemo Fetal Monitoring System (Nemo Healthcare, Veldhoven, The Netherlands), use only five and six electrodes, respectively. More recently, Imec and BloomLife showcased a fetal ECG and mobile wearable monitoring device featuring the first integrated circuit produced for this reason, which uses only five channels.
Because in this study we focused on evaluating the extraction of the maternal component, to perform this analysis, we adopted the following metrics:
a. The signal-to-interference ratio (SIR), which is more appropriate than SNR when the noise is a well-defined interference superimposed onto the signal of interest;
b. mECG attenuation after adaptive filtering, to enable better quantify how much of the maternal ECG is removed from the abdominal leads;
c. Fetal QRS peak detection accuracy, since fHR is the simplest parameter that can be extracted from the fECG.
SIR is often used to analyze the power in both the enhanced and rejected signal sources, for example when blind-source separation algorithms are benchmarked [19]. Since in this case the signal of interest was the fECG, whereas the interference was the mECG, the SIR was computed as follows:
SIRdB=20∗log10(AppfAppm) | (13) |
where Appm is the peak-to-peak amplitude of the maternal average QRS complex and Appf is the peak-to-peak amplitude of the average fetal QRS complex. Since the primary aim of using an adaptive filter with thoracic references is the removal of maternal ECG interference from the abdominal leads, the SIR parameter quantifies this cancellation process more effectively than other performance metrics. In Eq (13), the authors computed the peak-to-peak amplitudes based on the average QRS complex for both the fECG and mECG, because the local variability due to noise and small movements influences this computation. In this study, we annotated the fetal QRS complexes with the help of the simultaneous PWD signal, whereas we detected the maternal QRS using the Pan-Tompkins algorithm [33] on the horizontal chest lead.
To obtain a significant SIR, we performed QRS averaging only between complexes exhibiting a maximum of cross-correlation, based on the Pearson's correlation coefficient above a given threshold, which was chosen empirically to be equal to 0.6 to take into account the presence of noise. We set the time window for the fetal-QRS-complex template to 40 ms, as reported in [34], and that for the maternal QRS complex to 100 ms [35]. If fewer than four QRS complexes were recognized as being similar to the output signal, based on their cross-correlation values that signal (either fECG or mECG) could be treated as non-deterministic. In such an event, in Eq (13), the authors substituted the App peak-to-peak amplitude of the signal with four times its standard deviation, thus treating the signal as non-deterministic. Regarding the mECG, this situation occurs due to its adequate suppression, whereas for the fECG, it occurs due to the fact that fECG is not detectable on that lead.
By definition, the SIR is influenced by the amplitude of the signal and interference. The fECG amplitude depends on the fetal presentation, the developmental stage, and the composition of the feto-maternal compartment tissues. For this reason, we also computed the SIR on the raw signal to evaluate the performances of the SR and MR techniques by comparing their SIR values before and after applying the adaptive filter.
A high SIR implies good mECG cancellation from the abdominal recordings, whereas a low SIR indicates a trace in which the mECG signal power is still high, which means the maternal amplitudes are still significant in the processed signal with respect to the fECG. To enable quantification of the mECG removal, regardless of the fECG amplitude, we also computed the attenuation of the mECG as follows:
Attenuation=−20log10(AppoutAppin) | (14) |
where Appout is the peak-to-peak amplitude of the average maternal QRS complex in the processed abdominal signal and Appin is the peak-to-peak amplitude of the average maternal QRS complex in the original (unprocessed) abdominal lead.
Moreover, since the SIR is inherently influenced by both the fetal and maternal QRS amplitudes, to decouple these aspects, we evaluated both the fetal and maternal QRS amplitudes (in the original abdominal leads and in their SR and MR processed leads).
Finally, we used the jqrs fetal QRS detector [36] on all the processed abdominal leads to obtain the fHR. This algorithm consists of a window-based peak energy detector based on adaptive thresholding and forward and backward searches. We chose this algorithm from the fetal QRS detectors available in the scientific literature because it performed better in the training phase than others on fECG traces that have a very low SNR. The accuracy (Acc) of the peak detector for all the signals was computed as follows:
Acc=(TP+TN)/(TP+TN+FP+FN) | (16) |
where TP is the number of true positive detections, TN is the number of true negatives, FP is the number of false positives, and FN is the number of false negatives.
All the processing was performed in Matlab. To represent the metrics that provided some hints about the actual shape of their distributions, we selected the box-and-whiskers plot. In this plot, the median is highlighted, the box indicates the 25th and 75th percentiles, and the whiskers extend to the most extreme data points that are not considered to be outliers. Furthermore, we performed a statistical analysis to investigate the significance of the differences between the SR and MR results in terms of SIR, mECG attenuation, and fetal QRS detector accuracy. To do so, we considered the abdominal leads separately. First, we used the Lilliefors test to check the normality of the distributions. If the result does not satisfy the assumption of normal distribution, a non-parametric statistical test was adopted to determine the significance of the results. In particular, we chose the Wilcoxon signed rank test, considering a significance level p < 0.05.
In Figures 8–10 and Table 1, we grouped the results for the original (raw, OR) abdominal channels (i.e., the unfiltered ones) and the SR and MR processed leads, respectively, for the horizontal (hor), vertical (ver), oblique (obl), and unipolar (unip) abdominal leads. In these figures, the distributions of the results are shown as boxplots to provide a visual representation of the results, and the table shows the median and first and third quartile values of all the distributions.
SIR [dB] | Fetal Amp [µV] | matAmp [µV] | matAtt [dB] | QRSdetAcc | ||
Real dataset results | OR hor | -8.5(-12.09 -4.97) | 33.17(24.18 39.89) | 83.37(62.20 144.04) | ||
SR hor | -0.87(-7.39 2.23) | 32.14(24.61 36.42) | 28.97(23.00 69.61) | 15.02(9.11 21.50) | 0.62(0.50 0.84) | |
MR hor | 1.79(-1.20 5.17) | 30.61(25.83 37.10) | 24.75(13.71 32.91) | 25.75(19.80 33.41) | 0.85(0.77 0.94) | |
OR ver | -9.92(-12.79 -6.26) | 25.7(21.64 34.56) | 77.6(54.84 119.37) | |||
SR ver | -4.85(-8.91 -0.93) | 26.13(19.26 31.89) | 44.17(20.26 68.48) | 12.08(7.32 19.76) | 0.69(0.52 0.88) | |
MR ver | -0.06(-3.26 5.46) | 23.14(17.33 28.57) | 18.55(10.59 30.33) | 33.79(23.17 38.06) | 0.92(0.82 0.96) | |
OR obl | -13.05(-16.88 -5-76) | 38.45(29.91 46.66) | 142.47(74.90 246.37) | |||
SR obl | -5.48(-9.50 -0.39) | 34.81(24.95 42.67) | 60.68(33.25 107.82) | 13.99(7.88 20.71) | 0.61(0.52 0.84) | |
MR obl | 2.03(-2.78 4.92) | 33.46(24.63 43.78) | 27.38(17.92 40.94) | 35.09(26.38 41.31) | 0.89(0.77 0.92) | |
OR unip | -11.4(-13.72 -6.11) | 19.84(17.48 29.82) | 76.86(51.94 123.54) | |||
SR unip | -6.72(-8.60 -0.89) | 20.71(15.74 28.58) | 43.95(18.24 67.64) | 12.16(9.86 18.20) | 0.7(0.51 0.90) | |
MR unip | 2.63(-3.63 7.11) | 19.11(13.19 25.23) | 14.52(7.10 30.39) | 31.5(24.98 40.63) | 0.86(0.79 0.91) | |
Synthetic dataset results | OR hor | -12.8(-9.71 -15.84) | 0.63(0.44 0.90) | 2.78(2.75 2.81) | ||
SR hor | -7.32(-11.03 -4.59) | 0.51(0.33 0.70) | 1.18(1.16 1.19) | 8.57(8.46 8.78) | 0.9(0.82 0.96) | |
MR hor | 6.8(2.42 10.53) | 0.42(0.24 0.63) | 0.17(0.10 0.30) | 28.25(22.41 32.79) | 0.94(0.81 0.96) | |
OR ver | -8.61(-13.90 -4.50) | 0.14(0.08 0.21) | 0.37(0.37 0.38) | |||
SR ver | -2.8(-7.83 1.98) | 0.11(0.07 0.20) | 0.16(0.15 0.17) | 8.35(8.08 8.67) | 0.92(0.84 0.96) | |
MR ver | 8.73(2.93 13.19) | 0.12(0.06 0.20) | 0.04(0.03 0.06) | 21.1(17.43 26.59) | 0.92(0.89 0.96) | |
OR obl | -9.83(-13.15 -7.05) | 0.64(0.43 0.86) | 1.99(1.96 2.02) | |||
SR obl | -3.75(-7.76 -0.44) | 0.55(0.36 0.83) | 0.87(0.86 0.89) | 8.23(8.06 8.50) | 0.92(0.84 0.96) | |
MR obl | 8.53(3.27 12.69) | 0.52(0.26 0.81) | 0.18(0.11 0.32) | 24.36(18.39 28.90) | 0.92(0.84 0.96) | |
OR unip | -2.57(-5.83 -1.15) | 0.92(0.74 1.04) | 1.23(1.04 1.71) | |||
SR unip | 4.81(2.80 8.05) | 0.85(0.71 0.98) | 0.45(0.35 0.57) | 11.58(7.77 13.72) | 0.93(0.89 0.96) | |
MR unip | 6.79(5.05 10.87) | 0.84(0.69 0.96) | 0.36(0.24 0.45) | 13.79(9.20 16.91) | 0.96(0.92 0.96) |
First, we compare the performances of the SR and MR methods, and later our focus shifts to compare the different leads.
Figure 8 shows the overall results for the real dataset. We can see that the SIR values always show an improvement with respect to the raw signal, regardless of the channel or the chosen approach, but the MR adaptive filter significantly outperforms the SR (p < 0.0009). Remarkably, the significantly poor performance of the SR adaptive filter was confirmed when we considered the horizontal abdominal lead, even though the reference and processed leads were in parallel positions. Similar results were obtained for the SIR, as shown in Figure 9 for the synthetic dataset (p < 0.0002). By evaluating the mECG attenuation, it was possible to see how the MR approach significantly outperformed the SR implementation again (p < 0.0001), whichever lead was used.
Figures 8 and 9 also show the fetal and maternal QRS amplitudes, respectively, for the real and synthetic datasets. It is clear that the values of these two parameters decreased after adaptive filtering. Since we determined that the reference signals were not correlated with the fECG, because they were acquired on the upper part of the chest, the fECG attenuation can only be ascribed to both the frequency behavior of the filter and to a rough estimation of the fetal QRS amplitude on the original abdominal leads due to the larger maternal contributions. Moreover, the results for the fetal QRS amplitude in the real dataset reveal that the adoption of a differential measurement in the real recordings helped to increase the fECG amplitude from that of a unipolar lead (Figure 8). In fact, the median OR fetal amplitude values for the horizontal and oblique leads are higher than those of the unipolar channel. The differences between the distributions of these values are statistically significant (p = 0.004 for horizontal vs. unipolar, p = 0.001 for oblique vs. unipolar). This was also observed by the authors of [37], along with a reduction in the common-mode interference. The opposite behavior observed on the synthetic dataset (Figure 9) could lead to wrong conclusions. In fact, on synthetic signals, differential measurements generated reductions in the signals of both the fetal and maternal ECGs. This effect can be seen in Figure 11, which shows an example of the output synthetic signals.
Moreover, by looking at the SIR of the raw (OR) synthetic signals, it is clear that the lower values of the bipolar leads are comparable to those of the unipolar channel. Furthermore, both the fECG and the mECG are significantly smaller overall on the vertical lead, which is also evident in Figure 5. Moreover, the maternal amplitude was lower than the fECG amplitude, despite having set the SNRfm to -18 dB for the generation of the unipolar channels (from which the differential measurements were taken) to decrease this effect. In the real dataset, this never occurred, which suggests the need to be very careful when using a synthetic dataset for analyzing the performance of a fECG extraction algorithm.
Finally, on the real dataset, the accuracy of the fetal QRS detection (Figure 10, left) was significantly higher for the MR version of the adaptive filter than the SR version (p < 0.004). Moreover, the accuracy of the fetal QRS detection obtained from the SR output reveals the unreliability of this approach and strongly depends on the fECG amplitude. However, the difference between the two techniques (MR and SR) vanishes on the synthetic dataset (Figure 10, right, p < 0.8), because of the easy detectability of the synthetic fetal QRS from such signals, which is far from the reality.
To summarize the above findings, we performed a statistical analysis by the Wilcoxon test to enable a comparison of the MR and SR adaptive filters in terms of SIR. Tables 2 and 3 show the maternal attenuation and fetal QRS detection results on the separate channels for the real and synthetic datasets, respectively.
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0009* | 0.0001* | 0.0043* |
SR ver vs MR ver | 0.0003* | 0.0000* | 0.0009* |
SR obl vs MR obl | 0.0008* | 0.0000* | 0.0000* |
SR unip vs MR unip | 0.0006* | 0.0000* | 0.0001* |
SR vs MR | 0.0000* | 0.0000* | 0.0000* |
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0000* | 0.0000* | 0.4514 |
SR ver vs MR ver | 0.0000* | 0.0000* | 0.2055 |
SR obl vs MR obl | 0.0000* | 0.0000* | 0.4115 |
SR unip vs MR unip | 0.0002* | 0.0001* | 0.8280 |
SR vs MR | 0.0000* | 0.0000* | 0.5800 |
Finally, the above results enable an analysis of the behavior of the SR implementation for the different leads. Widrow et al. [16] asserted that maternal attenuation strongly depends on the electrode placement. In our dataset, the horizontal lead was parallel to the maternal lead taken as reference for the SR implementation and the results in terms of the SIR and maternal attenuation were significantly better than those obtained from the vertical oblique leads and unipolar channel on the real dataset. It is important to emphasize that the SIRs on the raw traces were similar for the different leads, with only the oblique lead having a lower value due to the stronger mECG contribution to that lead (Figure 8), even though the fetal QRS amplitude was also higher. However, on the synthetic traces, the performance of the SR method on the horizontal abdominal lead were not significantly better than those achieved on the other leads. In particular, the results on the oblique lead outperformed the others. Again, this result should serve as a warning regarding the adoption of simulated signals for this kind of evaluation.
In general, in terms of output signal quality, even though the MR adaptive filter output was better than that of the SR, it seemed to suffer from residual noise as well as power-line interference. As such, a post-processing stage is called for, which was beyond the scope of this work. Figure 12 shows an example of the output signals without any post-processing.
In this work, we systematically addressed the problem of the extraction of a fetal ECG from non-invasive recordings using QRD-RLS adaptive filters with single and multiple references. Since adaptive filters can be used when a reduced number of leads is needed to minimize setup complexity, especially in wearable applications, it is important to understand to what extent a SR adaptive filter can provide an adequate mECG attenuation that provides, at the least, a robust fetal QRS detection for fHR estimation. To this end, we tested SR and MR implementations of the same adaptive filter on real and synthetic signals and implemented up to three maternal thoracic references and four abdominal leads (three differential with 45 deg spacing, and one unipolar). The comparative analysis results confirmed the superiority of the MR as compared to the SR implementation (p < 0.0000) and the strong dependency of the latter on the electrode placement. Our quantitative results in terms of mECG attenuation and SIR values demonstrated how, by using multiple rather than single mECG reference leads even when dealing with a reference lead that is parallel to the abdominal lead, superior performance can always be achieved. Moreover, we found the accuracy of a fetal QRS detector applied to the output of the SR adaptive filter to be poor on real recordings (68% on average, σ = 0.0097). This means that SR approaches should be avoided in any case when trying to solve the non-invasive fECG extraction problem, even when the objective is to simply obtain the heart rate and even when a reference channel parallel to the abdominal channel is available. Overall, we can conclude that it is always worthwhile to use multiple rather than a single mECG reference lead when dealing with real non-invasive fECG recordings. It is also important to emphasize that the synthetic dataset in some cases led to results that were in direct contrast to the experimental evidence, which suggests that caution must be taken when using synthetic signals or, at least, in discussions of the results obtained by the algorithms for these datasets.
Secondly, the results of this study highlighted the better performance of differential measurements in enhancing the fECG amplitude, although they can also amplify the maternal interference, depending on the chosen abdominal lead. Finally, even the output of the best performing MR QRD-RLS algorithm seems to suffer from residual noise, beyond that of power-line interference, so we recommend the adoption of an ad-hoc denoising stage cascaded to the fECG extraction stage.
The authors wish to thank the team headed by Dr. Roberto Tumbarello, Division of Paediatric Cardiology, S. Michele Hospital (Cagliari, Italy), for the important support. We also wish to acknowledge all the involved voluntary pregnant women. Eleonora Sulas is grateful to Sardinia Regional Government for supporting her PhD scholarship (P.O.R. F.S.E., European Social Fund 2014–2020).
The authors declare no competing interests.
[1] | World health statistics 2023: monitoring health for the SDGs, sustainable development goals. Available from: https://www.who.int/publications/i/item/9789240074323 |
[2] | Noncommunicable diseases-World Health Organization (WHO) 2023 (16 September). Available from: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases |
[3] | Noncommunicable diseases-World Health Organization (WHO) 2023 (Dec 20). Available from: https://www.who.int/health-topics/noncommunicable-diseases#tab=tab_1 |
[4] |
Boutayeb A, Boutayeb S (2005) The burden of non communicable diseases in developing countries. Int J Equity Health 4: 2. https://doi.org/10.1186/1475-9276-4-2 ![]() |
[5] | Diabetes Prevention Program Research Group.Reduction in the Incidence of Type 2 Diabetes with Lifestyle Intervention or Metformin. N Engl J Med (2002) 346: 393-403. https://doi.org/10.1056/NEJMoa012512 |
[6] | Tsoupras A, Iatrou C, Frangia C, et al. (2009) The implication of platelet activating factor in cancer growth and metastasis: potent beneficial role of PAF-inhibitors and antioxidants. Infect Disord-Drug Targets Former Curr Drug Targets-Infect Disord 9: 390-399. https://doi.org/10.2174/187152609788922555 |
[7] |
Tsoupras A, Lordan R, Zabetakis I (2018) Inflammation, not cholesterol, is a cause of chronic disease. Nutrients 10: 604. https://doi.org/10.3390/nu10050604 ![]() |
[8] |
Tsoupras A, Lordan R, Zabetakis I (2019) Inflammation and cardiovascular diseases. The Impact of Nutrition and Statins on Cardiovascular Diseases . Elsevier 53-117. https://doi.org/10.1016/B978-0-12-813792-5.00003-3 ![]() |
[9] |
Nathan C, Ding A (2010) Nonresolving inflammation. Cell 140: 871-882. https://doi.org/10.1016/j.cell.2010.02.029 ![]() |
[10] |
Peluso I, Morabito G, Urban L, et al. (2012) Oxidative stress in atherosclerosis development: the central role of LDL and oxidative burst. Endocr Metab Immune Disord-Drug Targets 12: 351-360. https://doi.org/10.2174/187153012803832602 ![]() |
[11] |
Valko M, Leibfritz D, Moncol J, et al. (2007) Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39: 44-84. https://doi.org/10.1016/j.biocel.2006.07.001 ![]() |
[12] |
Koloverou E, Panagiotakos DB, Pitsavos C, et al. (2016) Adherence to Mediterranean diet and 10-year incidence (2002–2012) of diabetes: correlations with inflammatory and oxidative stress biomarkers in the ATTICA cohort study. Diabetes Metab Res Rev 32: 73-81. https://doi.org/10.1002/dmrr.2672 ![]() |
[13] |
Estruch R, Martínez-González MA, Corella D, et al. (2006) Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med 145: 1-11. https://doi.org/10.7326/0003-4819-145-1-200607040-00004 ![]() |
[14] | Zabetakis I, Lordan R, Tsoupras A, et al. Functional foods and their implications for health promotion, Academic Press (2022). https://doi.org/10.1016/B978-0-12-823811-0.00005-5 |
[15] | Tsoupras A, Panagopoulou EA, Kyzas GZ (2024) Anti-inflammatory, antithrombotic and anti-oxidant bioactives of beer and brewery by-products, as ingredients of bio-functional foods, nutraceuticals, cosmetics, cosmeceuticals and pharmaceuticals with health promoting properties. AIMS Agric Food . https://doi.org/10.3934/agrfood.2024032 |
[16] |
Tsoupras A, Ni VLJ, O'Mahony É, et al. (2023) Winemaking: “with one stone, two birds”? a holistic review of the bio-functional compounds, applications and health benefits of wine and wineries' by-products. Fermentation 9: 838. https://doi.org/10.3390/fermentation9090838 ![]() |
[17] |
Moran D, Fleming M, Daly E, et al. (2021) Anti-platelet properties of apple must/skin yeasts and of their fermented apple cider products. Beverages 7: 54. https://doi.org/10.3390/beverages7030054 ![]() |
[18] | Tsoupras A, Gkika D, Markopoulos T, et al. (2024) Apple products (apple juice and cider) and by-products (apple pomace): Bioactive compounds and biological properties. Springer . https://doi.org/10.1007/978-3-031-04195-2_214-1 |
[19] |
Conde TA, Zabetakis I, Tsoupras A, et al. (2021) Microalgal lipid extracts have potential to modulate the inflammatory response: a critical review. Int J Mol Sci 22: 9825. https://doi.org/10.3390/ijms22189825 ![]() |
[20] |
Tsoupras A, Davi KG (2024) Bioactive metabolites from fungi with anti-inflammatory and antithrombotic properties: current status and future perspectives for drug development. Fungi Bioactive Metabolites . Singapore: Springer Nature Singapore 427-494. https://doi.org/10.1007/978-981-99-5696-8_14 ![]() |
[21] |
Thiyagarasaiyar K, Goh BH, Jeon YJ, et al. (2020) Algae metabolites in cosmeceutical: an overview of current applications and challenges. Mar Drugs 18: 323. https://doi.org/10.3390/md18060323 ![]() |
[22] |
Chrzanowski G (2020) Saccharomyces Cerevisiae—an interesting producer of bioactive plant polyphenolic metabolites. Int J Mol Sci 21: 7343. https://doi.org/10.3390/ijms21197343 ![]() |
[23] | Culpepper T (2022) The effects of kefir and kefir components on immune and metabolic physiology in pre-clinical studies: a narrative review. Cureus . https://doi.org/10.7759/cureus.27768 |
[24] |
Apalowo OE, Adegoye GA, Mbogori T, et al. (2024) Nutritional characteristics, health impact, and applications of kefir. Foods 13: 1026. https://doi.org/10.3390/foods13071026 ![]() |
[25] |
Moretti AF, Moure MC, Quiñoy F, et al. (2022) Water kefir, a fermented beverage containing probiotic microorganisms: From ancient and artisanal manufacture to industrialized and regulated commercialization. Future Foods 5: 100123. https://doi.org/10.1016/j.fufo.2022.100123 ![]() |
[26] |
Marsh AJ, O'Sullivan O, Hill C, et al. (2013) Sequence-based analysis of the microbial composition of water kefir from multiple sources. FEMS Microbiol Lett 348: 79-85. https://doi.org/10.1111/1574-6968.12248 ![]() |
[27] |
Romero-Luna HE, Peredo-Lovillo A, Hernández-Mendoza A, et al. (2020) Probiotic potential of Lactobacillus paracasei CT12 isolated from water kefir grains (Tibicos). Curr Microbiol 77: 2584-2592. https://doi.org/10.1007/s00284-020-02016-0 ![]() |
[28] |
Peluzio MDCG, Dias MDME, Martinez JA, et al. (2021) Kefir and intestinal microbiota modulation: implications in human health. Front Nutr 8: 638740. https://doi.org/10.3389/fnut.2021.638740 ![]() |
[29] |
Zavala L, Golowczyc MA, Van Hoorde K, et al. (2016) Selected Lactobacillus strains isolated from sugary and milk kefir reduce Salmonella infection of epithelial cells in vitro. Benef Microbes 7: 585-595. https://doi.org/10.3920/BM2015.0196 ![]() |
[30] |
Zamberi NR, Abu N, Mohamed NE, et al. (2016) The antimetastatic and antiangiogenesis effects of kefir water on murine breast cancer cells. Integr Cancer Ther 15: NP53-NP66. https://doi.org/10.1177/1534735416642862 ![]() |
[31] |
Gamba RR, Yamamoto S, Sasaki T, et al. (2019) Microbiological and functional characterization of kefir grown in different sugar solutions. Food Sci Technol Res 25: 303-312. https://doi.org/10.3136/fstr.25.303 ![]() |
[32] | Koh WY, Utra U, Rosma A, et al. (2017) Development of a novel fermented pumpkin-based beverage inoculated with water kefir grains: a response surface methodology approach. Food Sci Biotechnol . https://doi.org/10.1007/s10068-017-0245-5 |
[33] |
Diniz RO, Garla LK, Schneedorf JM, et al. (2003) Study of anti-inflammatory activity of Tibetan mushroom, a symbiotic culture of bacteria and fungi encapsulated into a polysaccharide matrix. Pharmacol Res 47: 49-52. https://doi.org/10.1016/S1043-6618(02)00240-2 ![]() |
[34] |
Darvishzadeh P, Orsat V, Martinez JL (2021) Process optimization for development of a novel water kefir drink with high antioxidant activity and potential probiotic properties from russian olive fruit (Elaeagnus angustifolia). Food Bioprocess Technol 14: 248-260. https://doi.org/10.1007/s11947-020-02563-1 ![]() |
[35] | Yusuf D, Nuraida L, Dewanti-Hariyadi R, et al. (2020) In vitro antioxidant and α-Glucosidase inhibitory activities of Lactobacillus spp. isolated from indonesian kefir grains. Appl Food Biotechnol 8: 39-46. https://doi.org/10.22037/afb.v8i1.30367 |
[36] |
Mäkinen OE, Wanhalinna V, Zannini E, et al. (2016) Foods for special dietary needs: non-dairy plant-based milk substitutes and fermented dairy-type products. Crit Rev Food Sci Nutr 56: 339-349. https://doi.org/10.1080/10408398.2012.761950 ![]() |
[37] |
Fiorda FA, De Melo Pereira GV, Thomaz-Soccol V, et al. (2016) Development of kefir-based probiotic beverages with DNA protection and antioxidant activities using soybean hydrolyzed extract, colostrum and honey. LWT-Food Sci Technol 68: 690-697. https://doi.org/10.1016/j.lwt.2016.01.003 ![]() |
[38] |
Gulitz A, Stadie J, Wenning M, et al. (2011) The microbial diversity of water kefir. Int J Food Microbiol 151: 284-288. https://doi.org/10.1016/j.ijfoodmicro.2011.09.016 ![]() |
[39] | The ferment company Water Kefir Starter. Available from: https://www.thefermentcompany.nl/product/waterkefir-starter/ |
[40] | Hecer C, Ulusoy B, Kaynarca D (2019) Effect of different fermentation conditions on composition of kefir microbiota. Int Food Res J 26. Available from: https://www.researchgate.net/publication/333561113_Effect_of_different_fermentation_conditions_on_composition_of_kefir_microbiota |
[41] |
Verce M, De Vuyst L, Weckx S (2019) Shotgun metagenomics of a water kefir fermentation ecosystem reveals a novel oenococcus species. Front Microbiol 10: 479. https://doi.org/10.3389/fmicb.2019.00479 ![]() |
[42] |
Ziarno M, Bryś J, Kowalska E, et al. (2023) Effect of metabolic activity of lactic acid bacteria and propionibacteria on cheese protein digestibility and fatty acid profile. Sci Rep 13: 15363. https://doi.org/10.1038/s41598-023-42633-w ![]() |
[43] |
Karimkhani MM, Jamshidi A, Nasrollahzadeh M, et al. (2024) Fermentation of Rubus dolichocarpus juice using Lactobacillus gasseri and Lacticaseibacillus casei and protecting phenolic compounds by Stevia extract during cold storage. Sci Rep 14: 5711. https://doi.org/10.1038/s41598-024-56235-7 ![]() |
[44] |
Khan J, Sheoran S, Khan W, et al. (2020) Metabolic differentiation and quantification of gymnemic acid in GYMNEMA SYLVESTRE (Retz.) R.Br. ex Sm. leaf extract and its fermented products. Phytochem Anal 31: 488-500. https://doi.org/10.1002/pca.2912 ![]() |
[45] |
Sagdic O, Ozturk I, Yapar N, et al. (2014) Diversity and probiotic potentials of lactic acid bacteria isolated from gilaburu, a traditional Turkish fermented European cranberrybush (Viburnum opulus L.) fruit drink. Food Res Int 64: 537-545. https://doi.org/10.1016/j.foodres.2014.07.045 ![]() |
[46] |
Küçükgöz K, Kruk M, Kołożyn-Krajewska D, et al. (2024) Investigating the probiotic potential of vegan puree mixture: viability during simulated digestion and bioactive compound bioaccessibility. Nutrients 16: 561. https://doi.org/10.3390/nu16040561 ![]() |
[47] |
Tsai-Hsin C, Shwu-Jene T, Tsung-Yen W, et al. (2013) Improvement in antioxidant activity, angiotensin-converting enzyme inhibitory activity and in vitro cellular properties of fermented pepino milk by Lactobacillus strains containing the glutamate decarboxylase gene. J Sci Food Agric 93: 859-866. https://doi.org/10.1002/jsfa.5809 ![]() |
[48] |
Roman P, Carrillo-Trabalón F, Sánchez-Labraca N, et al. (2018) Are probiotic treatments useful on fibromyalgia syndrome or chronic fatigue syndrome patients? A systematic review. Benef Microbes 9: 603-611. https://doi.org/10.3920/bm2017.0125 ![]() |
[49] |
Lee SH, Cho DY, Lee SH, et al. (2019) A randomized clinical trial of synbiotics in irritable bowel syndrome: dose-dependent effects on gastrointestinal symptoms and fatigue. Korean J Fam Med 40: 2. https://doi.org/10.4082/kjfm.17.0064 ![]() |
[50] |
Peng M, Tabashsum Z, Patel P, et al. (2020) Prevention of enteric bacterial infections and modulation of gut microbiota with conjugated linoleic acids producing Lactobacillus in mice. Gut Microbes 11: 433-452. https://doi.org/10.1080/19490976.2019.1638724 ![]() |
[51] |
Kumar MR, Yeap SK, Mohamad NE, et al. (2021) Metagenomic and phytochemical analyses of kefir water and its subchronic toxicity study in BALB/c mice. BMC Complement Med Ther 21: 183. https://doi.org/10.1186/s12906-021-03358-3 ![]() |
[52] |
García-Ruiz A, Bartolomé B, Cueva C, et al. (2009) Inactivation of oenological lactic acid bacteria (Lactobacillus hilgardii and Pediococcus pentosaceus) by wine phenolic compounds. J Appl Microbiol 107: 1042-1053. https://doi.org/10.1111/j.1365-2672.2009.04287.x ![]() |
[53] |
Jurášková D, Ribeiro SC, Silva CCG (2022) Exopolysaccharides produced by lactic acid bacteria: from biosynthesis to health-promoting properties. Foods 11: 156. https://doi.org/10.3390/foods11020156 ![]() |
[54] |
Wang Y, Wu Y, Sailike J, et al. (2020) Fourteen composite probiotics alleviate type 2 diabetes through modulating gut microbiota and modifying M1/M2 phenotype macrophage in db/db mice. Pharmacol Res 161: 105150. https://doi.org/10.1016/j.phrs.2020.105150 ![]() |
[55] |
Yamaguchi T, Yasui K, Fujii S, et al. (2023) Lentilactobacillus hilgardii H-50 strongly inhibits lipopolysaccharide-induced inflammatory responses in mouse splenocytes via its specific surface layer proteins. J Appl Microbiol 134: lxad021. https://doi.org/10.1093/jambio/lxad021 ![]() |
[56] |
Xia T, Wang T, Sun J, et al. (2022) Modulation of fermentation quality and metabolome in co-ensiling of sesbania cannabina and sweet sorghum by lactic acid bacterial inoculants. Front Microbiol 13: 851271. https://doi.org/10.3389/fmicb.2022.851271 ![]() |
[57] |
Campos FM, Couto JA, Figueiredo AR, et al. (2009) Cell membrane damage induced by phenolic acids on wine lactic acid bacteria. Int J Food Microbiol 135: 144-151. https://doi.org/10.1016/j.ijfoodmicro.2009.07.031 ![]() |
[58] |
Campos FM, Figueiredo AR, Hogg TA, et al. (2009) Effect of phenolic acids on glucose and organic acid metabolism by lactic acid bacteria from wine. Food Microbiol 26: 409-414. https://doi.org/10.1016/j.fm.2009.01.006 ![]() |
[59] |
Xu D, Bechtner J, Behr J, et al. (2019) Lifestyle of Lactobacillus hordei isolated from water kefir based on genomic, proteomic and physiological characterization. Int J Food Microbiol 290: 141-149. https://doi.org/10.1016/j.ijfoodmicro.2018.10.004 ![]() |
[60] |
Bechtner J, Xu D, Behr J, et al. (2019) Proteomic analysis of Lactobacillus nagelii in the presence of Saccharomyces cerevisiae isolated from water kefir and comparison with Lactobacillus hordei. Front Microbiol 10: 325. https://doi.org/10.3389/fmicb.2019.00325 ![]() |
[61] |
Coniglio S, Shumskaya M, Vassiliou E (2023) Unsaturated fatty acids and their immunomodulatory properties. Biology 12: 279. https://doi.org/10.3390/biology12020279 ![]() |
[62] |
Carasi P, Racedo SM, Jacquot C, et al. (2015) Impact of Kefir Derived Lactobacillus kefiri on the mucosal immune response and gut microbiota. J Immunol Res 2015: 1-12. https://doi.org/10.1155/2015/361604 ![]() |
[63] |
Vieira LV, De Sousa LM, Maia TAC, et al. (2021) Milk Kefir therapy reduces inflammation and alveolar bone loss on periodontitis in rats. Biomed Pharmacother 139: 111677. https://doi.org/10.1016/j.biopha.2021.111677 ![]() |
[64] |
Toscano M, De Grandi R, Miniello VL, et al. (2017) Ability of Lactobacillus kefiri LKF01 (DSM32079) to colonize the intestinal environment and modify the gut microbiota composition of healthy individuals. Dig Liver Dis 49: 261-267. https://doi.org/10.1016/j.dld.2016.11.011 ![]() |
[65] |
Riaz Rajoka MS, Mehwish HM, Fang H, et al. (2019) Characterization and anti-tumor activity of exopolysaccharide produced by Lactobacillus kefiri isolated from Chinese kefir grains. J Funct Foods 63: 103588. https://doi.org/10.1016/j.jff.2019.103588 ![]() |
[66] |
Yerlikaya O, Akan E, Kinik Ö (2022) The metagenomic composition of water kefir microbiota. Int J Gastron Food Sci 30: 100621. https://doi.org/10.1016/j.ijgfs.2022.100621 ![]() |
[67] | Cunha C, Uecker JN, Jaskulski IB, et al. Probiotic characterization and safety assessment of Lactococcus Lactis Subsp. Lactis R7 isolated from ricotta cheese, in review. (2021). https://doi.org/10.21203/rs.3.rs-1135986/v1 |
[68] |
Kleerebezem M, Bachmann H, van Pelt-KleinJan E, et al. (2020) Lifestyle, metabolism and environmental adaptation in Lactococcus lactis. FEMS Microbiol Rev 44: 804-820. https://doi.org/10.1093/femsre/fuaa033 ![]() |
[69] |
Ayyash M, Olaimat A, Al-Nabulsi A, et al. (2020) Bioactive properties of novel probiotic Lactococcus lactis fermented camel sausages: cytotoxicity, angiotensin converting enzyme inhibition, antioxidant capacity, and antidiabetic activity. Food Sci Anim Resour 40: 155-171. https://doi.org/10.5851/kosfa.2020.e1 ![]() |
[70] |
Nishitani Y, Tanoue T, Yamada K, et al. (2009) Lactococcus lactis subsp. cremoris FC alleviates symptoms of colitis induced by dextran sulfate sodium in mice. Int Immunopharmacol 9: 1444-1451. https://doi.org/10.1016/j.intimp.2009.08.018 ![]() |
[71] |
Luerce TD, Gomes-Santos AC, Rocha CS, et al. (2014) Anti-inflammatory effects of Lactococcus lactis NCDO 2118 during the remission period of chemically induced colitis. Gut Pathog 6: 33. https://doi.org/10.1186/1757-4749-6-33 ![]() |
[72] |
Li P, Xu Y, Cao Y, et al. (2022) Polypeptides Isolated from Lactococcus lactis Alleviates lipopolysaccharide (lps)-induced inflammation in Ctenopharyngodon idella. Int J Mol Sci 23: 6733. https://doi.org/10.3390/ijms23126733 ![]() |
[73] |
Huang C, Kok J (2020) Editing of the proteolytic system of Lactococcus lactis increases its bioactive potential. Appl Environ Microbiol 86: e01319-20. https://doi.org/10.1128/AEM.01319-20 ![]() |
[74] |
Egea MB, Santos DCD, Oliveira Filho JGD, et al. (2022) A review of nondairy kefir products: their characteristics and potential human health benefits. Crit Rev Food Sci Nutr 62: 1536-1552. https://doi.org/10.1080/10408398.2020.1844140 ![]() |
[75] |
Kim S, Kim Y, Lee S, et al. (2022) Live biotherapeutic Lactococcus lactis GEN3013 enhances antitumor efficacy of cancer treatment via modulation of cancer progression and immune system. Cancers 14: 4083. https://doi.org/10.3390/cancers14174083 ![]() |
[76] |
De Castro CP, Drumond MM, Batista VL, et al. (2018) Vector development timeline for mucosal vaccination and treatment of disease using Lactococcus lactis and design approaches of next generation food grade plasmids. Front Microbiol 9: 1805. https://doi.org/10.3389/fmicb.2018.01805 ![]() |
[77] |
Benbouziane B, Ribelles P, Aubry C, et al. (2013) Development of a Stress-Inducible Controlled Expression (SICE) system in Lactococcus lactis for the production and delivery of therapeutic molecules at mucosal surfaces. J Biotechnol 168: 120-129. https://doi.org/10.1016/j.jbiotec.2013.04.019 ![]() |
[78] |
Martín R, Martín R, Chain F, et al. (2014) Effects in the use of a genetically engineered strain of Lactococcus lactis delivering in situ IL-10 as a therapy to treat low-grade colon inflammation. Hum Vaccines Immunother 10: 1611-1621. https://doi.org/10.4161/hv.28549 ![]() |
[79] |
Frossard CP, Steidler L, Eigenmann PA (2007) Oral administration of an IL-10–secreting Lactococcus lactis strain prevents food-induced IgE sensitization. J Allergy Clin Immunol 119: 952-959. https://doi.org/10.1016/j.jaci.2006.12.615 ![]() |
[80] |
Zurita-Turk M, Mendes Souza B, Prósperi De Castro C, et al. (2020) Attenuation of intestinal inflammation in IL-10 deficient mice by a plasmid carrying Lactococcus lactis strain. BMC Biotechnol 20: 38. https://doi.org/10.1186/s12896-020-00631-0 ![]() |
[81] |
Zurita-Turk M, Del Carmen S, Santos AC, et al. (2014) Lactococcus lactiscarrying the pValac DNA expression vector coding for IL-10 reduces inflammation in a murine model of experimental colitis. BMC Biotechnol 14: 73. https://doi.org/10.1186/1472-6750-14-73 ![]() |
[82] |
Wang J, Tian M, Li W, et al. (2019) Preventative delivery of IL-35 by Lactococcus lactis ameliorates DSS-induced colitis in mice. Appl Microbiol Biotechnol 103: 7931-7941. https://doi.org/10.1007/s00253-019-10094-9 ![]() |
[83] |
Bermúdez-Humarán LG, Langella P, Cortes-Perez NG, et al. (2003) Intranasal immunization with recombinant Lactococcus lactis secreting murine interleukin-12 enhances antigen-specific Th1 cytokine production. Infect Immun 71: 1887-1896. https://doi.org/10.1128/IAI.71.4.1887-1896.2003 ![]() |
[84] |
Koh WY, Uthumporn U, Rosma A, et al. (2018) Fermented pumpkin-based beverage inhibits key enzymes of carbohydrate digesting and extenuates postprandial hyperglycemia in type-2 diabetic rats. Acta Aliment 47: 495-503. https://doi.org/10.1556/066.2018.47.4.13 ![]() |
[85] |
Chen Y, Lin Y, Lin J, et al. (2018) Sugary kefir strain Lactobacillus mali APS1 ameliorated hepatic steatosis by regulation of SIRT-1/Nrf-2 and gut microbiota in rats. Mol Nutr Food Res 62: 1700903. https://doi.org/10.1002/mnfr.201700903 ![]() |
[86] |
Lin YC, Chen YT, Hsieh HH, et al. (2016) Effect of Lactobacillus mali APS1 and L. kefiranofaciens M1 on obesity and glucose homeostasis in diet-induced obese mice. J Funct Foods 23: 580-589. https://doi.org/10.1016/j.jff.2016.03.015 ![]() |
[87] |
Neville BA, Forde BM, Claesson MJ, et al. (2012) Characterization of pro-inflammatory flagellin proteins produced by Lactobacillus ruminis and related motile lactobacilli. PLoS ONE 7: e40592. https://doi.org/10.1371/journal.pone.0040592 ![]() |
[88] |
Lin YC, Chen YT, Li KY, et al. (2020) Investigating the mechanistic differences of obesity-inducing Lactobacillus kefiranofaciens M1 and Anti-obesity Lactobacillus mali APS1 by microbolomics and metabolomics. Front Microbiol 11: 1454. https://doi.org/10.3389/fmicb.2020.01454 ![]() |
[89] |
Hooi SL, Dwiyanto J, Toh KY, et al. (2023) The microbial composition and functional roles of different kombucha products in Singapore. CyTA-J Food 21: 269-274. https://doi.org/10.1080/19476337.2023.2190794 ![]() |
[90] |
Dong K, Li W, Xu Q, et al. (2023) Exploring the correlation of metabolites changes and microbial succession in solid-state fermentation of Sichuan Sun-dried vinegar. BMC Microbiol 23: 197. https://doi.org/10.1186/s12866-023-02947-1 ![]() |
[91] |
Rivera A, Becerra-Martinez E, Pacheco-Hernández Y, et al. (2020) Synergistic hypolipidemic and hypoglycemic effects of mixtures of Lactobacillus nagelii/betanin in a mouse model. Trop J Pharm Res 19: 1269-1276. https://doi.org/10.4314/tjpr.v19i6.23 ![]() |
[92] |
Yang J, Lagishetty V, Kurnia P, et al. (2022) Microbial and chemical profiles of commercial kombucha products. Nutrients 14: 670. https://doi.org/10.3390/nu14030670 ![]() |
[93] |
Mantzourani I, Terpou A, Bekatorou A, et al. (2022) Valorization of lactic acid fermentation of pomegranate juice by an acid tolerant and potentially probiotic lab isolated from kefir grains. Fermentation 8: 142. https://doi.org/10.3390/fermentation8040142 ![]() |
[94] |
Li Y, Song H, Zhang Z, et al. (2024) Effects of fermentation with different probiotics on the quality, isoflavone content, and flavor of okara beverages. Food Sci Nutr 12: 2619-2633. https://doi.org/10.1002/fsn3.3944 ![]() |
[95] |
Kim YB, Park J, Lee HG, et al. (2024) Dietary probiotic Lacticaseibacillus paracasei NSMJ56 modulates gut immunity and microbiota in laying hens. Poult Sci 103: 103505. https://doi.org/10.1016/j.psj.2024.103505 ![]() |
[96] |
Lee W, Im H, Lee YB, et al. (2024) Protective effect of soy germ-fermented postbiotics derived from Lacticaseibacillus paracasei DCF0429 (SGPB-DCF0429) in human reconstituted skin. J Funct Foods 113: 106023. https://doi.org/10.1016/j.jff.2024.106023 ![]() |
[97] |
Bhat B, Bajaj BK (2019) Hypocholesterolemic potential and bioactivity spectrum of an exopolysaccharide from a probiotic isolate Lactobacillus paracasei M7. Bioact Carbohydr Diet Fibre 19: 100191. https://doi.org/10.1016/j.bcdf.2019.100191 ![]() |
[98] |
Balzaretti S, Taverniti V, Guglielmetti S, et al. (2017) A novel rhamnose-rich hetero-exopolysaccharide isolated from Lactobacillus paracasei DG activates THP-1 human monocytic cells. Appl Environ Microbiol 83: e02702-16. https://doi.org/10.1128/AEM.02702-16 ![]() |
[99] |
Ahn H, Lee G, Lee W, et al. (2023) Evaluation of probiotic and anti-inflammatory properties of bacteriocinogenic Pediococcus acidilactici HW01 and Leuconostoc citreum HW02 from malted barley. Chem Biol Technol Agric 10: 49. https://doi.org/10.1186/s40538-023-00425-4 ![]() |
[100] |
Han HS, Soundharrajan I, Valan Arasu M, et al. (2023) Leuconostoc citreum inhibits adipogenesis and lipogenesis by inhibiting p38 MAPK/Erk 44/42 and stimulating AMPKα signaling pathways. Int J Mol Sci 24: 7367. https://doi.org/10.3390/ijms24087367 ![]() |
[101] |
Muthusamy K, Han HS, Soundharrajan I, et al. (2023) A novel strain of probiotic Leuconostoc citreum inhibits infection-causing bacterial pathogens. Microorganisms 11: 469. https://doi.org/10.3390/microorganisms11020469 ![]() |
[102] |
Son J, Jeong KJ (2022) Engineering of Leuconostoc citreum for efficient bioconversion of soy isoflavone glycosides to their aglycone forms. Int J Mol Sci 23: 9568. https://doi.org/10.3390/ijms23179568 ![]() |
[103] |
Li Y, Xiao L, Tian J, et al. (2022) Structural characterization, rheological properties and protection of oxidative damage of an exopolysaccharide from Leuconostoc citreum 1.2461 fermented in soybean whey. Foods 11: 2283. https://doi.org/10.3390/foods11152283 ![]() |
[104] |
Wang Y, Du R, Qiao X, et al. (2020) Optimization and characterization of exopolysaccharides with a highly branched structure extracted from Leuconostoc citreum B-2. Int J Biol Macromol 142: 73-84. https://doi.org/10.1016/j.ijbiomac.2019.09.071 ![]() |
[105] |
Kim M, Jang JK, Park YS (2021) Production optimization, structural analysis, and prebiotic- and anti-inflammatory effects of gluco-oligosaccharides produced by Leuconostoc lactis SBC001. Microorganisms 9: 200. https://doi.org/10.3390/microorganisms9010200 ![]() |
[106] |
Chang-Liao WP, Lee A, Chiu YH, et al. (2020) Isolation of a Leuconostoc mesenteroides strain with anti-porcine epidemic diarrhea virus activities from kefir grains. Front Microbiol 11: 1578. https://doi.org/10.3389/fmicb.2020.01578 ![]() |
[107] |
Luan C, Yan J, Jiang N, et al. (2022) Leuconostoc mesenteroides LVBH107 antibacterial activity against porphyromonas gingivalis and anti-inflammatory activity against P. gingivalis lipopolysaccharide-stimulated RAW 264.7 cells. Nutrients 14: 2584. https://doi.org/10.3390/nu14132584 ![]() |
[108] |
Moon HJ, Oh SH, Park KB, et al. (2023) Kimchi and Leuconostoc mesenteroides DRC 1506 alleviate dextran sulfate sodium (dss)-induced colitis via attenuating inflammatory responses. Foods 12: 584. https://doi.org/10.3390/foods12030584 ![]() |
[109] |
Zhang Q, Wang J, Sun Q, et al. (2021) Characterization and antioxidant activity of released exopolysaccharide from potential probiotic Leuconostoc mesenteroides LM187. J Microbiol Biotechnol 31: 1144-1153. https://doi.org/10.4014/jmb.2103.03055 ![]() |
[110] |
Li Y, Liu Y, Cao C, et al. (2020) Extraction and biological activity of exopolysaccharide produced by Leuconostoc mesenteroides SN-8. Int J Biol Macromol 157: 36-44. https://doi.org/10.1016/j.ijbiomac.2020.04.150 ![]() |
[111] |
Taylan O, Yilmaz MT, Dertli E (2019) Partial characterization of a levan type exopolysaccharide (EPS) produced by Leuconostoc mesenteroides showing immunostimulatory and antioxidant activities. Int J Biol Macromol 136: 436-444. https://doi.org/10.1016/j.ijbiomac.2019.06.078 ![]() |
[112] |
Hwang JE, Kim KT, Paik HD (2019) Improved antioxidant, anti-inflammatory, and anti-adipogenic properties of hydroponic ginseng fermented by Leuconostoc mesenteroides KCCM 12010P. Molecules 24: 3359. https://doi.org/10.3390/molecules24183359 ![]() |
[113] |
Daliri EB, Choi S, Cho B, et al. (2019) Biological activities of a garlic–Cirsium setidens Nakai blend fermented with Leuconostoc mesenteroides. Food Sci Nutr 7: 2024-2032. https://doi.org/10.1002/fsn3.1032 ![]() |
[114] |
Li Y, Liu L, Yu X, et al. (2019) Transglycosylation improved caffeic acid phenethyl ester anti-inflammatory activity and water solubility by Leuconostoc mesenteroides dextransucrase. J Agric Food Chem 67: 4505-4512. https://doi.org/10.1021/acs.jafc.9b01143 ![]() |
[115] | Murtaza G, Karim S, Akram MR, et al. (2014) Caffeic acid phenethyl ester and therapeutic potentials. BioMed Res Int 2014: 1-9. https://doi.org/10.1155/2014/145342 |
[116] |
Woo HJ, Kang HK, Nguyen TTH, et al. (2012) Synthesis and characterization of ampelopsin glucosides using dextransucrase from Leuconostoc mesenteroides B-1299CB4: Glucosylation enhancing physicochemical properties. Enzyme Microb Technol 51: 311-318. https://doi.org/10.1016/j.enzmictec.2012.07.014 ![]() |
[117] |
Ruiz-de-Villa C, Poblet M, Bordons A, et al. (2023) Comparative study of inoculation strategies of Torulaspora delbrueckii and Saccharomyces cerevisiae on the performance of alcoholic and malolactic fermentations in an optimized synthetic grape must. Int J Food Microbiol 404: 110367. https://doi.org/10.1016/j.ijfoodmicro.2023.110367 ![]() |
[118] |
Su J, Wang T, Li YY, et al. (2015) Antioxidant properties of wine lactic acid bacteria: Oenococcus oeni. Appl Microbiol Biotechnol 99: 5189-5202. https://doi.org/10.1007/s00253-015-6425-4 ![]() |
[119] |
Luciana Del Valle R, Carmen M, María José R-V, et al. (2022) Utilization of Oenococcus oeni strains to ferment grape juice: Metabolic activities and beneficial health potential. Food Microbiol 101: 103895. https://doi.org/10.1016/j.fm.2021.103895 ![]() |
[120] |
Kristof I, Ledesma SC, Apud GR, et al. (2023) Oenococcus oeni allows the increase of antihypertensive and antioxidant activities in apple cider. Heliyon 9: e16806. https://doi.org/10.1016/j.heliyon.2023.e16806 ![]() |
[121] |
Foligné B, Dewulf J, Breton J, et al. (2010) Probiotic properties of non-conventional lactic acid bacteria: Immunomodulation by Oenococcus oeni. Int J Food Microbiol 140: 136-145. https://doi.org/10.1016/j.ijfoodmicro.2010.04.007 ![]() |
[122] |
Hossain S, Khetra Y, Dularia C, et al. (2023) Symbiotic fermentation study of Acetobacter orientalis and lactic acid bacteria for lactobionic acid enriched yoghurt production. Food Biosci 53: 102612. https://doi.org/10.1016/j.fbio.2023.102612 ![]() |
[123] |
Gamba RR, Yamamoto S, Abdel-Hamid M, et al. (2020) Chemical, microbiological, and functional characterization of kefir produced from cow's milk and soy milk. Int J Microbiol 2020: 1-11. https://doi.org/10.1155/2020/7019286 ![]() |
[124] |
Aligita W, Singgih M, Sutrisno E, et al. (2023) Hepatoprotective properties of water kefir: A traditional fermented drink and its potential role. Int J Prev Med 14: 93. https://doi.org/10.4103%2Fijpvm.ijpvm_29_22 ![]() |
[125] |
Cai C, Li Z, Lu J, et al. (2023) Effects of acetoin on growth performance, digestive function, antioxidant status, and immune capacity of largemouth bass (Micropterus salmoides). Aquac Res 2023: 1-12. https://doi.org/10.1155/2023/6114525 ![]() |
[126] |
Michiels J, Truffin D, Majdeddin M, et al. (2023) Gluconic acid improves performance of newly weaned piglets associated with alterations in gut microbiome and fermentation. Porc Health Manag 9: 10. https://doi.org/10.1186/s40813-023-00305-1 ![]() |
[127] |
Fischer F, Romero R, Hellhund A, et al. (2020) Dietary cellulose induces anti-inflammatory immunity and transcriptional programs via maturation of the intestinal microbiota. Gut Microbes 12: 1829962. https://doi.org/10.1080/19490976.2020.1829962 ![]() |
[128] |
White KM, Matthews MK, Hughes RC, et al. (2018) A metagenome-wide association study and arrayed mutant library confirm Acetobacter lipopolysaccharide genes are necessary for association with Drosophila melanogaster. G3 GenesGenomesGenetics 8: 1119-1127. https://doi.org/10.1534/g3.117.300530 ![]() |
[129] |
Kong Y, Wang L, Jiang B (2021) The role of gut microbiota in aging and aging related neurodegenerative disorders: insights from drosophila model. Life 11: 855. https://doi.org/10.3390/life11080855 ![]() |
[130] |
Batista LL, Malta SM, Guerra Silva HC, et al. (2021) Kefir metabolites in a fly model for Alzheimer's disease. Sci Rep 11: 11262. https://doi.org/10.1038/s41598-021-90749-8 ![]() |
[131] |
Kim D, Kim H, Seo K (2020) Microbial composition of Korean kefir and antimicrobial activity of Acetobacter fabarum DH1801. J Food Saf 40: e12728. https://doi.org/10.1111/jfs.12728 ![]() |
[132] |
Martínez-Torres A, Gutiérrez-Ambrocio S, Heredia-del-Orbe P, et al. (2017) Inferring the role of microorganisms in waterkefirfermentations. Int J Food Sci Technol 52: 559-571. https://doi.org/10.1111/ijfs.13312 ![]() |
[133] |
Uchida K, Akashi K, Motoshima H, et al. (2009) Microbiota analysis of Caspian Sea yogurt, a ropy fermented milk circulated in Japan. Anim Sci J 80: 187-192. https://doi.org/10.1111/j.1740-0929.2008.00607.x ![]() |
[134] |
Eble H, Joswig M, Lamberti L, et al. (2023) Master regulators of biological systems in higher dimensions. Proc Natl Acad Sci 120: e2300634120. https://doi.org/10.1073/pnas.2300634120 ![]() |
[135] |
Hou Z, Sun L, Wang D, et al. (2020) Production of 2-keto-gluconic acid from glucose by immobilized Pseudomonas plecoglossicida resting cells. 3 Biotech 10: 253. https://doi.org/10.1007/s13205-020-02243-z ![]() |
[136] |
Goderska K (2019) The antioxidant and prebiotic properties of lactobionic acid. Appl Microbiol Biotechnol 103: 3737-3751. https://doi.org/10.1007/s00253-019-09754-7 ![]() |
[137] |
Arrieta-Echeverri MC, Fernandez GJ, Duarte-Riveros A, et al. (2023) Multi-omics characterization of the microbial populations and chemical space composition of a water kefir fermentation. Front Mol Biosci 10: 1223863. https://doi.org/10.3389/fmolb.2023.1223863 ![]() |
[138] | Kusnadi J, Tirtania AR, Arumingtyas EL (2023) Antioxidant activity, physicochemical characterisation and antibacterial properties of caspian sea yoghurt enriched with ginger and sappanwood extracts. Trop J Nat Prod Res 7. http://www.doi.org/10.26538/tjnpr/v7i3.11 |
[139] |
Lee S, Lee JA, Park GG, et al. (2017) Semi-continuous fermentation of onion vinegar and its functional properties. Molecules 22: 1313. https://doi.org/10.3390/molecules22081313 ![]() |
[140] |
Lim JM, Lee SH, Jeong DY, et al. (2022) Significance of LED lights in enhancing the production of vinegar using Acetobacter pasteurianus AP01. Prep Biochem Biotechnol 52: 38-47. https://doi.org/10.1080/10826068.2021.1907406 ![]() |
[141] |
Taweekasemsombut S, Tinoi J, Mungkornasawakul P, et al. (2021) Thai rice vinegars: production and biological properties. Appl Sci 11: 5929. https://doi.org/10.3390/app11135929 ![]() |
[142] |
Liu X, Zhang L, Cao C, et al. (2023) Biorefining process of agricultural onions to functional vinegar. Prep Biochem Biotechnol 53: 424-432. https://doi.org/10.1080/10826068.2022.2098321 ![]() |
[143] |
Luang-In V, Saengha W, Yotchaisarn M, et al. (2018) Microbial strains and bioactive exopolysaccharide producers from Thai Water Kefir. Microbiol Biotechnol Lett 46: 403-415. https://doi.org/10.4014/mbl.1804.04019 ![]() |
[144] |
Wen X, Wang Z, Liu Q, et al. (2023) Acetobacter pasteurianus BP2201 alleviates alcohol-induced hepatic and neuro-toxicity and modulate gut microbiota in mice. Microb Biotechnol 16: 1834-1857. https://doi.org/10.1111/1751-7915.14303 ![]() |
[145] |
Ankrah NYD, Barker BE, Song J, et al. (2021) Predicted metabolic function of the gut microbiota of Drosophila melanogaster. mSystems 6: e01369-20. https://doi.org/10.1128/mSystems.01369-20 ![]() |
[146] |
Huang JH, Douglas AE (2015) Consumption of dietary sugar by gut bacteria determines Drosophila lipid content. Biol Lett 11: 20150469. https://doi.org/10.1098/rsbl.2015.0469 ![]() |
[147] | Tokatli Demi̇Rok N, Alpaslan M, Yikmiş S (2023) Some lactobacillus, leuconostoc and acetobacter strains in traditional turkish yoghurt, cheese, kefir samples as a probiotic candidate. Int J Agric Environ Food Sci 7: 326-334. https://doi.org/10.31015/jaefs.2023.2.10 |
[148] |
Purutoğlu K, İspirli H, Yüzer MO, et al. (2020) Diversity and functional characteristics of lactic acid bacteria from traditional kefir grains. Int J Dairy Technol 73: 57-66. https://doi.org/10.1111/1471-0307.12633 ![]() |
[149] |
Milani C, Lugli GA, Duranti S, et al. (2014) Genomic encyclopedia of type strains of the genus bifidobacterium. Appl Environ Microbiol 80: 6290-6302. https://doi.org/10.1128/AEM.02308-14 ![]() |
[150] |
Laureys D, Cnockaert M, De Vuyst L, et al. (2016) Bifidobacterium aquikefiri sp. nov., isolated from water kefir. Int J Syst Evol Microbiol 66: 1281-1286. https://doi.org/10.1099/ijsem.0.000877 ![]() |
[151] |
Laureys D, Van Jean A, Dumont J, et al. (2017) Investigation of the instability and low water kefir grain growth during an industrial water kefir fermentation process. Appl Microbiol Biotechnol 101: 2811-2819. https://doi.org/10.1007/s00253-016-8084-5 ![]() |
[152] |
Patel SH, Tan JP, Börner RA, et al. (2022) A temporal view of the water kefir microbiota and flavour attributes. Innov Food Sci Emerg Technol 80: 103084. https://doi.org/10.1016/j.ifset.2022.103084 ![]() |
[153] |
Manosalva C, Quiroga J, Hidalgo AI, et al. (2022) Role of lactate in inflammatory processes: friend or foe. Front Immunol 12: 808799. https://doi.org/10.3389/fimmu.2021.808799 ![]() |
[154] |
Cavone L, Calosi L, Cinci L, et al. (2012) Topical mannitol reduces inflammatory edema in a rat model of arthritis. Pharmacology 89: 18-21. https://doi.org/10.1159/000335094 ![]() |
[155] |
Pelle E, Mammone T, Marenus K, et al. (2003) Ultraviolet-b-induced oxidative DNA base damage in primary normal human epidermal keratinocytes and inhibition by a hydroxyl radical scavenger. J Invest Dermatol 121: 177-183. https://doi.org/10.1046/j.1523-1747.2003.12330.x ![]() |
[156] |
Ratter JM, Rooijackers HMM, Hooiveld GJ, et al. (2018) In vitro and in vivo effects of lactate on metabolism and cytokine production of human primary pbmcs and monocytes. Front Immunol 9: 2564. https://doi.org/10.3389/fimmu.2018.02564 ![]() |
[157] |
Eckel VPL, Vogel RF (2020) Genomic and physiological insights into the lifestyle of Bifidobacterium species from water kefir. Arch Microbiol 202: 1627-1637. https://doi.org/10.1007/s00203-020-01870-7 ![]() |
[158] |
Grosser N, Oberle S, Berndt G, et al. (2004) Antioxidant action of l-alanine: heme oxygenase-1 and ferritin as possible mediators. Biochem Biophys Res Commun 314: 351-355. https://doi.org/10.1016/j.bbrc.2003.12.089 ![]() |
[159] |
Pires RS, Braga PGS, Santos JMB, et al. (2021) l-Glutamine supplementation enhances glutathione peroxidase and paraoxonase-1 activities in HDL of exercising older individuals. Exp Gerontol 156: 111584. https://doi.org/10.1016/j.exger.2021.111584 ![]() |
[160] | Moradi M, Moradi B, Hashemian AH, et al. (2022) Beneficial effect of L-Proline supplementation on the quality of human spermatozoa. Andrologia 54. https://doi.org/10.1111/and.14486 |
[161] |
Abbasi M, Taheri Mirghaed A, Hoseini SM, et al. (2023) Effects of dietary glycine supplementation on growth performance, immunological, and erythrocyte antioxidant parameters in common carp, Cyprinus carpio. Animals 13: 412. https://doi.org/10.3390/ani13030412 ![]() |
[162] |
Zhang D, Nie S, Xie M, et al. (2020) Antioxidant and antibacterial capabilities of phenolic compounds and organic acids from Camellia oleifera cake. Food Sci Biotechnol 29: 17-25. ![]() |
[163] |
Schöpping M, Zeidan AA, Franzén CJ (2022) Stress response in bifidobacteria. Microbiol Mol Biol Rev 86: e00170-21. https://doi.org/10.1007%2Fs10068-019-00637-1 ![]() |
[164] | Younus H (2018) Therapeutic potentials of superoxide dismutase. Int J Health Sci 12: 88. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/pmc5969776/ |
[165] | Sarıkaya E, Doğan S (2020) Glutathione peroxidase in health and diseases. Glutathione System and Oxidative Stress in Health and Disease . IntechOpen. https://doi.org/10.5772/intechopen.91009 |
[166] |
Gulitz A, Stadie J, Ehrmann MA, et al. (2013) Comparative phylobiomic analysis of the bacterial community of water kefir by 16S rRNA gene amplicon sequencing and ARDRA analysis. J Appl Microbiol 114: 1082-1091. https://doi.org/10.1111/jam.12124 ![]() |
[167] |
Delcenserie V, Gavini F, Beerens H, et al. (2007) Description of a new species, Bifidobacterium crudilactis sp. nov., isolated from raw milk and raw milk cheeses. Syst Appl Microbiol 30: 381-389. https://doi.org/10.1016/j.syapm.2007.01.004 ![]() |
[168] |
Delcenserie V, Taminiau B, Gavini F, et al. (2013) Detection and characterization of Bifidobacterium crudilactis and B. mongoliense able to grow during the manufacturing process of French raw milk cheeses. BMC Microbiol 13: 239. https://doi.org/10.1186/1471-2180-13-239 ![]() |
[169] |
Bondue P, Lebrun S, Taminiau B, et al. (2020) Effect of Bifidobacterium crudilactis and 3′-sialyllactose on the toddler microbiota using the SHIME® model. Food Res Int 138: 109755. https://doi.org/10.1016/j.foodres.2020.109755 ![]() |
[170] |
Yao Y, Cai X, Fei W, et al. (2022) The role of short-chain fatty acids in immunity, inflammation and metabolism. Crit Rev Food Sci Nutr 62: 1-12. https://doi.org/10.1080/10408398.2020.1854675 ![]() |
[171] |
Wu J, Chen N, Grau E, et al. (2024) Short chain fatty acids inhibit corneal inflammatory responses to TLR ligands via the ocular G-protein coupled receptor 43. Ocul Surf 32: 48-57. https://doi.org/10.1016/j.jtos.2024.01.005 ![]() |
[172] |
Jiang M, Li Z, Zhang F, et al. (2023) Butyrate inhibits iILC2-mediated lung inflammation via lung-gut axis in chronic obstructive pulmonary disease (COPD). BMC Pulm Med 23: 163. https://doi.org/10.1186/s12890-023-02438-z ![]() |
[173] |
Sato Y, Kanayama M, Nakajima S, et al. (2024) Sialyllactose enhances the short-chain fatty acid production and barrier function of gut epithelial cells via nonbifidogenic modification of the fecal microbiome in human adults. Microorganisms 12: 252. https://doi.org/10.3390/microorganisms12020252 ![]() |
[174] |
Gökırmaklı Ç, Yüceer YK, Guzel-Seydim ZB (2023) Chemical, microbial, and volatile changes of water kefir during fermentation with economic substrates. Eur Food Res Technol 249: 1717-1728. https://doi.org/10.1007/s00217-023-04242-9 ![]() |
[175] |
Laureys D, De Vuyst L (2014) Microbial species diversity, community dynamics, and metabolite kinetics of water kefir fermentation. Appl Environ Microbiol 80: 2564-2572. https://doi.org/10.1128/AEM.03978-13 ![]() |
[176] | Raimondi S, Amaretti A, Leonardi A, et al. (2016) Conjugated linoleic acid production by bifidobacteria: screening, kinetic, and composition. BioMed Res Int 2016: 1-8. https://doi.org/10.1155/2016/8654317 |
[177] |
Valenzuela CA, Baker EJ, Miles EA, et al. (2023) Conjugated linoleic acids have anti-inflammatory effects in cultured endothelial cells. Int J Mol Sci 24: 874. https://doi.org/10.3390/ijms24010874 ![]() |
[178] |
Huang WC, Tu RS, Chen YL, et al. (2016) Conjugated linoleic acids suppress inflammatory response and ICAM-1 expression through inhibition of NF-κB and MAPK signaling in human bronchial epithelial cells. Food Funct 7: 2025-2033. https://doi.org/10.1039/C5FO01037C ![]() |
[179] |
Wijaya L, Sumerta IN, Napitupulu TP, et al. (2024) Cultural, nutritional and microbial perspectives of tuak, a traditional Balinese beverage. J Ethn Foods 11: 1-14. https://doi.org/10.1186/s42779-024-00221-x ![]() |
[180] | Rogers P, Jeon Y, Lee K, et al. (2007) Zymomonas mobilis for fuel ethanol and higher value products. Biofuels 263–288. https://doi.org/10.1007/10_2007_060 |
[181] | Kim KH, Chung CB, Kim YH, et al. (2005) Cosmeceutical properties of levan produced by Zymomonas mobilis. J Cosmet Sci 56: 395-406. http://dx.doi.org/10.1111/j.1467-2494.2006.00314_2.x |
[182] |
Dawes E, Ribbons D, Rees D (1966) Sucrose utilization by Zymomonas mobilis: formation of a levan. Biochem J 98: 804. https://doi.org/10.1042/bj0980804 ![]() |
[183] | Scopes R (1987) Zymomonas as a source of diagnostic enzymes. Aust J Biotechnol 1: 58-63. Available from: https://scholar.google.com/scholar_lookup?&title=Zymomonas%20as%20a%20source%20of%20diagnostic%20enzymes&journal=Aust.%20J.%20Biotechnol&volume=1&issue=3&pages=58-63&publication_year=1987&author=Scopes%2CRK |
[184] |
Uhlenbusch I, Sahm H, Sprenger GA (1991) Expression of an L-alanine dehydrogenase gene in Zymomonas mobilis and excretion of L-alanine. Appl Environ Microbiol 57: 1360-1366. https://doi.org/10.1128/aem.57.5.1360-1366.1991 ![]() |
[185] | Kim JY, Shin SH, Chong HY, et al. Transformant for production of lactic acid of high optical purity and method for producing lactic acid using the same (2016). Available from: https://patents.google.com/patent/US9428775B2/en |
[186] |
Misawa N, Yamano S, Ikenaga H (1991) Production of beta-carotene in Zymomonas mobilis and Agrobacterium tumefaciens by introduction of the biosynthesis genes from Erwinia uredovora. Appl Environ Microbiol 57: 1847-1849. https://doi.org/10.1128%2Faem.57.6.1847-1849.1991 ![]() |
[187] |
Liebler DC, Stratton SP, Kaysen KL (1997) Antioxidant actions of β-carotene in liposomal and microsomal membranes: role of carotenoid-membrane incorporation and α-tocopherol. Arch Biochem Biophys 338: 244-250. https://doi.org/10.1006/abbi.1996.9822 ![]() |
[188] | Yang Y, Li R, Hui J, et al. (2021) β-Carotene attenuates LPS-induced rat intestinal inflammation via modulating autophagy and regulating the JAK2/STAT3 and JNK/p38 MAPK signaling pathways. J Food Biochem 45. https://doi.org/10.1111/jfbc.13544 |
[189] |
Tornabene TG, Holzer G, Bittner AS, et al. (1982) Characterization of the total extractable lipids of Zymomonas mobilis var. mobilis. Can J Microbiol 28: 1107-1118. https://doi.org/10.1139/m82-165 ![]() |
[190] |
Carey VC, Ingram LO (1983) Lipid composition of Zymomonas mobilis: effects of ethanol and glucose. J Bacteriol 154: 1291-1300. https://doi.org/10.1128/jb.154.3.1291-1300.1983 ![]() |
[191] |
Barrow KD, Collins JG, Rogers PL, et al. (1983) Lipid composition of an ethanol-tolerant strain of Zymomonas mobilis. Biochim Biophys Acta BBA-Lipids Lipid Metab 753: 324-330. https://doi.org/10.1016/0005-2760(83)90055-3 ![]() |
[192] |
Khalil ASM, Giribabu N, Yelumalai S, et al. (2021) Myristic acid defends against testicular oxidative stress, inflammation, apoptosis: Restoration of spermatogenesis, steroidogenesis in diabetic rats. Life Sci 278: 119605. https://doi.org/10.1016/j.lfs.2021.119605 ![]() |
[193] |
Zadeh Hashem E, Khodadadi M, Asadi F, et al. (2016) The antioxidant activity of palmitoleic acid on the oxidative stress parameters of palmitic acid in adult rat cardiomyocytes. Ann Mil Health Sci Res 14. https://doi.org/10.5812/amh.11467 ![]() |
[194] |
Tsai YW, Lu CH, Chang RCA, et al. (2021) Palmitoleic acid ameliorates palmitic acid-induced proinflammation in J774A.1 macrophages via TLR4-dependent and TNF-α-independent signallings. Prostaglandins Leukot Essent Fatty Acids 169: 102270. https://doi.org/10.1016/j.plefa.2021.102270 ![]() |
[195] |
Wang Z, Liang C, Li G, et al. (2007) Stearic acid protects primary cultured cortical neurons against oxidative stress. Acta Pharmacol Sin 28: 315-326. https://doi.org/10.1111/j.1745-7254.2007.00512.x ![]() |
[196] |
Pan PH, Lin SY, Ou YC, et al. (2010) Stearic acid attenuates cholestasis-induced liver injury. Biochem Biophys Res Commun 391: 1537-1542. https://doi.org/10.1016/j.bbrc.2009.12.119 ![]() |
[197] |
Alves NFB, de Queiroz TM, de Almeida Travassos R, et al. (2017) Acute treatment with lauric acid reduces blood pressure and oxidative stress in spontaneously hypertensive rats. Basic Clin Pharmacol Toxicol 120: 348-353. https://doi.org/10.1111/bcpt.12700 ![]() |
[198] | Dubo A, Dawud F, Umar I, et al. (2019) Lauric acid alleviates inflammation and structural changes in the lungs of type II diabetic male Wistar rats. J Afr Assoc Physiol Sci 7: 88-96. Available from: https://www.ajol.info/index.php/jaaps/article/view/192646 |
[199] |
Tsoupras AB, Demopoulos CA, Pappas KM (2012) Platelet-activating factor detection, metabolism, and inhibitors in the ethanologenic bacterium Zymomonas mobilis. Eur J Lipid Sci Technol 114: 123-133. https://doi.org/10.1002/ejlt.201000489 ![]() |
[200] |
Campos IA, Ximenes EA, Carvalho Júnior CHR, et al. (2013) Zymomonas mobilis culture protects against sepsis by modulating the inflammatory response, alleviating bacterial burden and suppressing splenocyte apoptosis. Eur J Pharm Sci 48: 1-8. https://doi.org/10.1016/j.ejps.2012.10.011 ![]() |
[201] |
Diaz M, Kellingray L, Akinyemi N, et al. (2019) Comparison of the microbial composition of African fermented foods using amplicon sequencing. Sci Rep 9: 13863. https://doi.org/10.1038/s41598-019-50190-4 ![]() |
[202] | Lindner P Atlas der mikroskopischen Grundlagen der Garungskunde, Tafel 68 (1928). Available from: https://scholar.google.com/scholar?hl=el&as_sdt=0%2C5&q=Lindner%2C+P.+%281928%29.+Atlas+der+mikroskopischen+Grundlagen+der+Garungskunde%2C+Tafel+68.&btnG= |
[203] | Millis NF Some bacterial fermentations of cider (1951). Available from: https://scholar.google.com/scholar?hl=el&as_sdt=0%2C5&q=Millis%2C+N.+F.+%281951%29.+Some+bacterial+fermentations+of+cider.&btnG= |
[204] |
Ruiz-Argueso T, Rodriguez-Navarro A (1975) Microbiology of ripening honey. Appl Microbiol 30: 893-896. https://doi.org/10.1128%2Fam.30.6.893-896.1975 ![]() |
[205] |
Fentie EG, Jeong M, Emire SA, et al. (2022) Physicochemical properties, antioxidant activities and microbial communities of Ethiopian honey wine, Tej. Food Res Int 152: 110765. https://doi.org/10.1016/j.foodres.2021.110765 ![]() |
[206] |
Fabricio MF, Mann MB, Kothe CI, et al. (2022) Effect of freeze-dried kombucha culture on microbial composition and assessment of metabolic dynamics during fermentation. Food Microbiol 101: 103889. https://doi.org/10.1016/j.fm.2021.103889 ![]() |
[207] |
Kawamata Y, Toyotake Y, Ogiyama D, et al. (2021) Development of the original whey-based vinegar using rapeseed meal or wheat bran as a raw material for koji. J Food Process Preserv 45. https://doi.org/10.1111/jfpp.16097 ![]() |
[208] |
Wang B, Rutherfurd-Markwick K, Liu N, et al. (2024) Evaluation of the probiotic potential of yeast isolated from kombucha in New Zealand. Curr Res Food Sci 8: 100711. https://doi.org/10.1016/j.crfs.2024.100711 ![]() |
[209] | Cosmetic composition containing polyorganosiloxane-containing epsilon-polylysine polymer, and polyhydric alcohol, and production thereof. Available from: https://patents.google.com/patent/EP1604647A1/en |
[210] |
Lam R, Lin ZX, Sviderskaya E, et al. (2014) Mechanistic studies of anti-hyperpigmentary compounds: elucidating their inhibitory and regulatory actions. Int J Mol Sci 15: 14649-14668. https://doi.org/10.3390/ijms150814649 ![]() |
[211] |
Köhler S, Schmacht M, Troubounis AHL, et al. (2021) Tradition as a stepping stone for a microbial defined water kefir fermentation process: insights in cell growth, bioflavoring, and sensory perception. Front Microbiol 12: 732019. https://doi.org/10.3389/fmicb.2021.732019 ![]() |
[212] |
Kim H, Hur S, Lim J, et al. (2023) Enhancement of the phenolic compounds and antioxidant activities of Kombucha prepared using specific bacterial and yeast. Food Biosci 56: 103431. https://doi.org/10.1016/j.fbio.2023.103431 ![]() |
[213] |
Vigentini I, Romano A, Compagno C, et al. (2008) Physiological and oenological traits of different Dekkera/Brettanomyces bruxellensis strains under wine-model conditions. FEMS Yeast Res 8: 1087-1096. https://doi.org/10.1111/j.1567-1364.2008.00395.x ![]() |
[214] |
Silva LR, Andrade PB, Valentão P, et al. (2005) Analysis of non-coloured phenolics in red wine: Effect of Dekkera bruxellensis yeast. Food Chem 89: 185-189. https://doi.org/10.1016/j.foodchem.2004.02.019 ![]() |
[215] |
Schifferdecker AJ, Dashko S, Ishchuk OP, et al. (2014) The wine and beer yeast Dekkera bruxellensis. Yeast 31: 323-332. https://doi.org/10.1002/yea.3023 ![]() |
[216] |
Sun TY, Li JS, Chen C (2015) Effects of blending wheatgrass juice on enhancing phenolic compounds and antioxidant activities of traditional kombucha beverage. J Food Drug Anal 23: 709-718. https://doi.org/10.1016/j.jfda.2015.01.009 ![]() |
[217] |
Lee J, Cho J, Kim J, et al. (2022) Evaluation of the fermentation characteristics and functionality of kombucha for commercialization. J Korean Soc Food Sci Nutr 51: 811-818. https://doi.org/10.3746/jkfn.2022.51.8.811 ![]() |
[218] |
Tran T, Roullier-Gall C, Verdier F, et al. (2022) Microbial interactions in kombucha through the lens of metabolomics. Metabolites 12: 235. https://doi.org/10.3390/metabo12030235 ![]() |
[219] |
Tran T, Billet K, Torres-Cobos B, et al. (2022) Use of a minimal microbial consortium to determine the origin of kombucha flavor. Front Microbiol 13: 836617. https://doi.org/10.3389/fmicb.2022.836617 ![]() |
[220] |
Lalitha P, Parthiban A, Sachithanandam V, et al. (2021) Antibacterial and antioxidant potential of GC-MS analysis of crude ethyl acetate extract from the tropical mangrove plant Avicennia officinalis L. South Afr J Bot 142: 149-155. https://doi.org/10.1016/j.sajb.2021.06.023 ![]() |
[221] |
Bellut K, Krogerus K, Arendt EK (2020) Lachancea fermentati strains isolated from kombucha: fundamental insights, and practical application in low alcohol beer brewing. Front Microbiol 11: 764. https://doi.org/10.3389/fmicb.2020.00764 ![]() |
[222] |
Maciel NOP, Piló FB, Freitas LFD, et al. (2013) The diversity and antifungal susceptibility of the yeasts isolated from coconut water and reconstituted fruit juices in Brazil. Int J Food Microbiol 160: 201-205. https://doi.org/10.1016/j.ijfoodmicro.2012.10.012 ![]() |
[223] |
Leuck AM, Rothenberger MK, Green JS (2014) Fungemia due to Lachancea fermentati: a case report. BMC Infect Dis 14: 250. https://doi.org/10.1186/1471-2334-14-250 ![]() |
[224] |
Fakruddin Md, Hossain MdN, Ahmed MM (2017) Antimicrobial and antioxidant activities of Saccharomyces cerevisiae IFST062013, a potential probiotic. BMC Complement Altern Med 17: 64. https://doi.org/10.1186/s12906-017-1591-9 ![]() |
[225] |
Eppinga H, Thio HB, Schreurs MWJ, et al. (2017) Depletion of Saccharomyces cerevisiae in psoriasis patients, restored by Dimethylfumarate therapy (DMF). PLOS ONE 12: e0176955. https://doi.org/10.1371/journal.pone.0176955 ![]() |
[226] |
Gabrielli E, Pericolini E, Ballet N, et al. (2018) Saccharomyces cerevisiae-based probiotic as novel anti-fungal and anti-inflammatory agent for therapy of vaginal candidiasis. Benef Microbes 9: 219-230. https://doi.org/10.3920/BM2017.0099 ![]() |
[227] |
Ye S, Shen F, Jiao L, et al. (2020) Biosynthesis of selenoproteins by Saccharomyces cerevisiae and characterization of its antioxidant activities. Int J Biol Macromol 164: 3438-3445. https://doi.org/10.1016/j.ijbiomac.2020.08.144 ![]() |
[228] |
Babaei M, Borja Zamfir GM, Chen X, et al. (2020) Metabolic engineering of Saccharomyces cerevisiae for rosmarinic acid production. ACS Synth Biol 9: 1978-1988. https://doi.org/10.1021/acssynbio.0c00048 ![]() |
[229] |
Callari R, Fischer D, Heider H, et al. (2018) Biosynthesis of angelyl-CoA in Saccharomyces cerevisiae. Microb Cell Factories 17: 72. https://doi.org/10.1186/s12934-018-0925-8 ![]() |
[230] |
Sun S, Xu X, Liang L, et al. (2021) Lactic acid-producing probiotic Saccharomyces cerevisiae attenuates ulcerative colitis via suppressing macrophage pyroptosis and modulating gut microbiota. Front Immunol 12: 777665. https://doi.org/10.3389/fimmu.2021.777665 ![]() |
[231] |
Hu Q, Yu L, Zhai Q, et al. (2023) Anti-inflammatory, barrier maintenance, and gut microbiome modulation effects of Saccharomyces cerevisiae QHNLD8L1 on dss-induced ulcerative colitis in mice. Int J Mol Sci 24: 6721. https://doi.org/10.3390/ijms24076721 ![]() |
[232] | Fragopoulou E, Antonopoulou S, Tsoupras A, et al. Antiatherogenic properties of red/white wine, musts, grape-skins, and yeast, 25–29 (2004). Available from: https://scholar.google.com/scholar?hl=el&as_sdt=0%2C5&q=Fragopoulou%2C+E.%2C+Antonopoulou%2C+S.%2C+Tsoupras%2C+A.%2C+Tsantila%2C+N.%2C+Grypioti%2C+A.%2C+Gribilas%2C+G.%2C+Gritzapi%2C+H.%2C+Konsta%2C+E.%2C+Skandalou%2C+E.%2C+%26+Papadopoulou%2C+A.+%282004%29.+Antiatherogenic+properties+of+red%2Fwhite+wine%2C+musts%2C+grape-skins%2C+and+yeast.+25%E2%80%9329.&btnG= |
[233] |
Csoma H, Acs-Szabo L, Papp LA, et al. (2023) Characterization of Zygosaccharomyces lentus yeast in hungarian botrytized wines. Microorganisms 11: 852. https://doi.org/10.3390/microorganisms11040852 ![]() |
[234] |
Castro L, Gómez-Álvarez H, González F, et al. (2023) Biorecovery of rare earth elements from fluorescent lamp powder using the fungus Aspergillus niger in batch and semicontinuous systems. Miner Eng 201: 108215. https://doi.org/10.1016/j.mineng.2023.108215 ![]() |
[235] |
Steels H, James SA, Roberts IN, et al. (1999) Zygosaccharomyces lentus: a significant new osmophilic, preservative-resistant spoilage yeast, capable of growth at low temperature: H. STEELS ET AL. J Appl Microbiol 87: 520-527. https://doi.org/10.1046/j.1365-2672.1999.00844.x ![]() |
[236] | Mcmeeking A, Dieckmann E, Cheeseman C (2024) Production methods for bacterial biomaterials: A review. Mater Today Sustain 25: 100623. https://doi.org/10.1016/j.mtsust.2023.100623 |
[237] |
Stadie J, Gulitz A, Ehrmann MA, et al. (2013) Metabolic activity and symbiotic interactions of lactic acid bacteria and yeasts isolated from water kefir. Food Microbiol 35: 92-98. https://doi.org/10.1016/j.fm.2013.03.009 ![]() |
[238] |
Gientka I, Kieliszek M, Jermacz K, et al. (2017) Identification and characterization of oleaginous yeast isolated from kefir and its ability to accumulate intracellular fats in deproteinated potato wastewater with different carbon sources. BioMed Res Int 2017: 1-19. https://doi.org/10.1155/2017/6061042 ![]() |
[239] |
Lencioni L, Romani C, Gobbi M, et al. (2016) Controlled mixed fermentation at winery scale using Zygotorulaspora florentina and Saccharomyces cerevisiae. Int J Food Microbiol 234: 36-44. https://doi.org/10.1016/j.ijfoodmicro.2016.06.004 ![]() |
[240] |
Hosseini M, Sharifan A (2021) Biological properties of yeast-based mannoprotein for prospective biomedical applications. Comb Chem High Throughput Screen 24: 831-840. https://doi.org/10.2174/1386207323999200818162030 ![]() |
[241] | Alsayadi M, Al Jawfi Y, Belarbi M, et al. (2013) Antioxidant potency of water kefir. J Microbiol Biotechnol Food Sci 2: 2444-2447. Available from: https://office2.jmbfs.org/index.php/JMBFS/article/view/7101 |
[242] | Constantin EA, Popa-Tudor I, Matei F, et al. Evaluation of polyphenol content and antioxidant activity of standard water kefir, NeXT-Chem 2023, MDPI, 7. (2023). https://doi.org/10.3390/chemproc2023013007 |
[243] | Vamsnu E, Dangnon DB (2023) Characterizing water kefir beverages with antioxidant effects: preliminary analysis. Sci Bull Ser F Biotechnol 27. Available from: https://biotechnologyjournal.usamv.ro/pdf/2023/issue_2/Art12.pdf |
[244] |
Güzel-Seydim ZB, Şatır G, Gökırmaklı Ç (2023) Use of mandarin and persimmon fruits in water kefir fermentation. Food Sci Nutr 11: 5890-5897. https://doi.org/10.1002/fsn3.3561 ![]() |
[245] |
Falsoni RMP, Moraes FDSA, Rezende MSD, et al. (2022) Pretreatment with water kefir reduces the development of acidified ethanol-induced gastric ulcers. Braz J Pharm Sci 58: e191046. https://doi.org/10.1590/s2175-97902022e191046 ![]() |
[246] |
Diniz RO, Perazzo FF, Carvalho JCT, et al. (2003) Atividade antiinflamatória de quefir, um probiótico da medicina popular. Rev Bras Farmacogn 13: 19-21. https://doi.org/10.1590/S0102-695X2003000300008 ![]() |
[247] |
Rodrigues KL, Carvalho JCT, Schneedorf JM (2005) Anti-inflammatory properties of kefir and its polysaccharide extract. InflammoPharmacology 13: 485-492. https://doi.org/10.1163/156856005774649395 ![]() |
[248] | Aligita W, Tarigan PN, Susilawati E (2020) Anti inflammatory and antioxidant activity of kefir water. Int J Biol Pharm Allied Sci 9. https://doi.org/10.31032/IJBPAS/2020/9.1.4904 |
[249] | Aligita A, Si WM Anti inflammatory and antioxidant activity of kefir water (2022). Available from: https://scholar.google.com/scholar?hl=el&as_sdt=0%2C5&q=ALIGITA%2C+A.%2C+%26+Si%2C+W+M.+%282022%29.+Anti+inflammatory+and+antioxidant+activity+of+kefir+water.&btnG= |
[250] |
Calatayud M, Börner RA, Ghyselinck J, et al. (2021) Water kefir and derived pasteurized beverages modulate gut microbiota, intestinal permeability and cytokine production In Vitro. Nutrients 13: 3897. https://doi.org/10.3390/nu13113897 ![]() |
[251] |
Talib N, Mohamad NE, Yeap SK, et al. (2019) Isolation and characterization of Lactobacillus spp. from kefir samples in Malaysia. Molecules 24: 2606. https://doi.org/10.3390/molecules24142606 ![]() |
[252] |
Gökırmaklı Ç, Erol Z, Gun I, et al. (2023) Prophylaxis effects of water kefir on post-infectious irritable bowel syndrome in rat model. Int J Food Sci Technol 58: 3371-3378. https://doi.org/10.1111/ijfs.16310 ![]() |
[253] |
Guven M, Akman T, Yener AU, et al. (2015) The neuroprotective effect of kefir on spinal cord ischemia/reperfusion injury in rats. J Korean Neurosurg Soc 57: 335. https://doi.org/10.3340/jkns.2015.57.5.335 ![]() |
[254] |
Yurtal Z, Kutlu T, Altuğ M, et al. (2022) Investigation of the neuroprotective effect of kefir in experimental spinal cord injury. Ank Üniversitesi Vet Fakültesi Derg 70: 9-19. https://doi.org/10.33988/auvfd.872947 ![]() |
[255] |
Kumar M, Yeap S, Lee H, et al. (2021) Selected kefir water from Malaysia attenuates hydrogen peroxide-induced oxidative stress by upregulating endogenous antioxidant levels in SH-SY5Y neuroblastoma cells. Antioxidants 10: 940. https://doi.org/10.3390/antiox10060940 ![]() |
[256] |
Alsayadi M, Jawfi YA, Belarbi M, et al. (2014) Evaluation of anti-hyperglycemic and anti-hyperlipidemic activities of water kefir as probiotic on streptozotocin-induced diabetic wistar rats. J Diabetes Mellit 04: 85-95. https://doi.org/10.4236/jdm.2014.42015 ![]() |
[257] |
Rocha-Gomes A, Escobar A, Soares JS, et al. (2018) Chemical composition and hypocholesterolemic effect of milk kefir and water kefir in Wistar rats. Rev Nutr 31: 137-145. https://doi.org/10.1590/1678-98652018000200001 ![]() |
[258] |
Aligita W, Singgih M, Sutrisno E, et al. (2023) Hepatoprotective study of Indonesian water kefir against CCl4-induced liver injury in rats. J Pharm Pharmacogn Res 11: 1002-1016. https://doi.org/10.56499/jppres23.1732_11.6.1002 ![]() |
[259] |
Ye Z, Yang X, Deng B, et al. (2023) Prevention of DSS-induced colitis in mice with water kefir microbiota via anti-inflammatory and microbiota-balancing activity. Food Funct 14: 6813-6827. https://doi.org/10.1039/D3FO00354J ![]() |
[260] |
Moreira MEC, Santos MHD, Zolini GPP, et al. (2008) Anti-inflammatory and cicatrizing activities of a carbohydrate fraction isolated from sugary kefir. J Med Food 11: 356-361. https://doi.org/10.1089/jmf.2007.329 ![]() |
[261] | Aligita W, Singgih M, Sutrisno E, et al. (2023) Protein-protein interaction analysis to identify nuclear factor-erythroid-2 factor 2 (nrf2) inhibition by extracellular enzymes from water kefir organisms. Int J Appl Pharm 109–112. https://doi.org/10.22159/ijap.2023.v15s2.20 |
[262] |
Rodrigues KL, Caputo LRG, Carvalho JCT, et al. (2005) Antimicrobial and healing activity of kefir and kefiran extract. Int J Antimicrob Agents 25: 404-408. https://doi.org/10.1016/j.ijantimicag.2004.09.020 ![]() |
[263] |
Brasil GA, Andrade Moraes FS, Prucoli Falsoni RM, et al. (2019) Pretreatment with water kefir promotes a decrease in ulcer development in an ethanol-acidified ulcer model. FASEB J 33: 760-762. https://doi.org/10.1096/fasebj.2019.33.1_supplement.760.2 ![]() |
[264] |
Rodrigues KL, Araújo TH, Schneedorf JM, et al. (2016) A novel beer fermented by kefir enhances anti-inflammatory and anti-ulcerogenic activities found isolated in its constituents. J Funct Foods 21: 58-69. http://dx.doi.org/10.1016/j.jff.2015.11.035 ![]() |
[265] |
Mechmeche M, Ksontini H, Hamdi M, et al. (2019) Production of bioactive peptides in tomato seed protein isolate fermented by water kefir culture: optimization of the fermentation conditions. Int J Pept Res Ther 25: 137-150. https://doi.org/10.1007/s10989-017-9655-8 ![]() |
[266] |
Azi F, Tu C, Meng L, et al. (2021) Metabolite dynamics and phytochemistry of a soy whey-based beverage bio-transformed by water kefir consortium. Food Chem 342: 128225. https://doi.org/10.1016/j.foodchem.2020.128225 ![]() |
[267] |
Ozcelik F, Akan E, Kinik O (2021) Use of Cornelian cherry, hawthorn, red plum, roseship and pomegranate juices in the production of water kefir beverages. Food Biosci 42: 101219. https://doi.org/10.1016/j.fbio.2021.101219 ![]() |
[268] |
Bueno RS, Ressutte JB, Hata NNY, et al. (2021) Quality and shelf life assessment of a new beverage produced from water kefir grains and red pitaya. LWT 140: 110770. https://doi.org/10.1016/j.lwt.2020.110770 ![]() |
[269] |
Alrosan M, Tan TC, Easa AM, et al. (2023) Evaluation of quality and protein structure of natural water kefir-fermented quinoa protein concentrates. Food Chem 404: 134614. https://doi.org/10.1016/j.foodchem.2022.134614 ![]() |
[270] |
Şafak H, Gün İ, Tudor Kalit M, et al. (2023) Physico-chemical, microbiological and sensory properties of water kefir drinks produced from demineralized whey and dimrit and shiraz grape varieties. Foods 12: 1851. https://doi.org/10.3390/foods12091851 ![]() |
[271] |
Wang X, Wang P (2023) Red beetroot juice fermented by water kefir grains: physicochemical, antioxidant profile and anticancer activity. Eur Food Res Technol 249: 939-950. https://doi.org/10.1007/s00217-022-04185-7 ![]() |
[272] |
Islamiana D, Prabowo R, Pramaningtyas MD (2020) The effect of orange water kefir on malondialdehyde (MDA) level and superoxide dismutase (SOD) inhibition rate in kidney tissue of the hyperlipidemic rat (Rattus norvegicus). Atherosclerosis 315: e264. https://doi.org/10.1016/j.atherosclerosis.2020.10.833 ![]() |
[273] | Aspiras BEE, Flores R, Pareja MC (2015) Hepatoprotective effect of Fermented Water Kefir on Sprague-Dawley rats (Rattus norvegicus) induced with sublethal dose of Acetaminophen. Int J Curr Sci 17: 18-28. Available from: https://d1wqtxts1xzle7.cloudfront.net/47094518/Bea_Eunice-libre.pdf?1467943173=&response-content-disposition=inline%3B+filename%3DHepatoprotective_effect_of_Fermented_Wat.pdf&Expires=1725024033&Signature=e4qEln3fmYio4UeuPM8Qpo4pUYFf7rD~NSZA7u2tTveBvZ6TFh1b-LDYrMQG2PI4mYiReptaTHXIcsHFYxRXQSH5HPsyP-ceiPiLdd2VI0RyYBbhjheFE-ZB6aqkyg7AbpVsvH-UFu6n-ith9vB5lh1SYPqPh88M8EshTAwzWZePMMrHnD4V057tNH2IeOYJalMhHT4PfhQhSsU4DRz6eZoxgTdS~KPYHtdtVu1ZUGmrTGMua90YB3uyOhLK4JjH3tZhTkEyVgGnyNnZYaaQrBEmx22BbgEpC6~xlp-OvKvHGu-MaIlbZ~Pnq03PxXxgUP3VTi8W8I65CGfVuRe-Mg__&Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA |
[274] | Tiss M, Souiy Z, Abdeljelil NB, et al. (2020) Fermented soy milk prepared using kefir grains prevents and ameliorates obesity, type 2 diabetes, hyperlipidemia and Liver-Kidney toxicities in HFFD-rats. J FunctFoods 67: 103869. https://doi.org/10.1016/j.jff.2020.103869 |
1. | Giulia Baldazzi, Eleonora Sulas, Monica Urru, Roberto Tumbarello, Luigi Raffo, Danilo Pani, Annotated real and synthetic datasets for non-invasive foetal electrocardiography post-processing benchmarking, 2020, 33, 23523409, 106399, 10.1016/j.dib.2020.106399 | |
2. | Giulia Baldazzi, Eleonora Sulas, Monica Urru, Roberto Tumbarello, Luigi Raffo, Danilo Pani, Wavelet denoising as a post-processing enhancement method for non-invasive foetal electrocardiography, 2020, 195, 01692607, 105558, 10.1016/j.cmpb.2020.105558 | |
3. | Eleonora Sulas, Monica Urru, Roberto Tumbarello, Luigi Raffo, Reza Sameni, Danilo Pani, A non-invasive multimodal foetal ECG–Doppler dataset for antenatal cardiology research, 2021, 8, 2052-4463, 10.1038/s41597-021-00811-3 | |
4. | Radek Martinek, Radana Kahankova, Rene Jaros, Katerina Barnova, Adam Matonia, Michal Jezewski, Robert Czabanski, Krzysztof Horoba, Janusz Jezewski, Non-Invasive Fetal Electrocardiogram Extraction Based on Novel Hybrid Method for Intrapartum ST Segment Analysis, 2021, 9, 2169-3536, 28608, 10.1109/ACCESS.2021.3058733 | |
5. | Jingyu Hao, Yuyao Yang, Zhuhuang Zhou, Shuicai Wu, Fetal Electrocardiogram Signal Extraction Based on Fast Independent Component Analysis and Singular Value Decomposition, 2022, 22, 1424-8220, 3705, 10.3390/s22103705 | |
6. | Giulia Baldazzi, Eleonora Sulas, Rik Vullings, Monica Urru, Roberto Tumbarello, Luigi Raffo, Danilo Pani, Automatic signal quality assessment of raw trans-abdominal biopotential recordings for non-invasive fetal electrocardiography, 2023, 11, 2296-4185, 10.3389/fbioe.2023.1059119 | |
7. | Giulia Baldazzi, Danilo Pani, 2024, Chapter 12, 978-3-031-32624-0, 221, 10.1007/978-3-031-32625-7_12 | |
8. | P.R. Barayazi, K.G. Samarawickrama, 2023, Analysis of Fetal ECG Signal Associated QRS Complex Features for Early Detection of Congenital Heart Diseases, 979-8-3503-2362-7, 197, 10.1109/ICIIS58898.2023.10253566 | |
9. | E. Sai Kumar, P. Thanapal, N Sai Kiran, Khariduhari Krishna, J Srinivasa Rao, G. Srinivasa Rao, 2023, Non-Invasive Foetal Electrocardiogram (ECG) Extraction Using Abdominal Electrocardiogram of the Mother, 979-8-3503-4595-7, 423, 10.1109/IHCSP56702.2023.10127124 | |
10. | Mohammed Moutaib, Mohammed Fattah, Yousef Farhaoui, Badraddine Aghoutane, Moulhime El Bekkali, Extraction of fetal electrocardiogram signal based on K-means Clustering, 2023, 2, 2953-4917, 84, 10.56294/dm202384 | |
11. | Shilpa Patil, T. Anne Ramya, Chat-GPT Powered IoT devices using regularizing the data for an efficient management systems, 2024, 2024, 2956-8323, 179, 10.2478/jsiot-2024-0020 |
SIR [dB] | Fetal Amp [µV] | matAmp [µV] | matAtt [dB] | QRSdetAcc | ||
Real dataset results | OR hor | -8.5(-12.09 -4.97) | 33.17(24.18 39.89) | 83.37(62.20 144.04) | ||
SR hor | -0.87(-7.39 2.23) | 32.14(24.61 36.42) | 28.97(23.00 69.61) | 15.02(9.11 21.50) | 0.62(0.50 0.84) | |
MR hor | 1.79(-1.20 5.17) | 30.61(25.83 37.10) | 24.75(13.71 32.91) | 25.75(19.80 33.41) | 0.85(0.77 0.94) | |
OR ver | -9.92(-12.79 -6.26) | 25.7(21.64 34.56) | 77.6(54.84 119.37) | |||
SR ver | -4.85(-8.91 -0.93) | 26.13(19.26 31.89) | 44.17(20.26 68.48) | 12.08(7.32 19.76) | 0.69(0.52 0.88) | |
MR ver | -0.06(-3.26 5.46) | 23.14(17.33 28.57) | 18.55(10.59 30.33) | 33.79(23.17 38.06) | 0.92(0.82 0.96) | |
OR obl | -13.05(-16.88 -5-76) | 38.45(29.91 46.66) | 142.47(74.90 246.37) | |||
SR obl | -5.48(-9.50 -0.39) | 34.81(24.95 42.67) | 60.68(33.25 107.82) | 13.99(7.88 20.71) | 0.61(0.52 0.84) | |
MR obl | 2.03(-2.78 4.92) | 33.46(24.63 43.78) | 27.38(17.92 40.94) | 35.09(26.38 41.31) | 0.89(0.77 0.92) | |
OR unip | -11.4(-13.72 -6.11) | 19.84(17.48 29.82) | 76.86(51.94 123.54) | |||
SR unip | -6.72(-8.60 -0.89) | 20.71(15.74 28.58) | 43.95(18.24 67.64) | 12.16(9.86 18.20) | 0.7(0.51 0.90) | |
MR unip | 2.63(-3.63 7.11) | 19.11(13.19 25.23) | 14.52(7.10 30.39) | 31.5(24.98 40.63) | 0.86(0.79 0.91) | |
Synthetic dataset results | OR hor | -12.8(-9.71 -15.84) | 0.63(0.44 0.90) | 2.78(2.75 2.81) | ||
SR hor | -7.32(-11.03 -4.59) | 0.51(0.33 0.70) | 1.18(1.16 1.19) | 8.57(8.46 8.78) | 0.9(0.82 0.96) | |
MR hor | 6.8(2.42 10.53) | 0.42(0.24 0.63) | 0.17(0.10 0.30) | 28.25(22.41 32.79) | 0.94(0.81 0.96) | |
OR ver | -8.61(-13.90 -4.50) | 0.14(0.08 0.21) | 0.37(0.37 0.38) | |||
SR ver | -2.8(-7.83 1.98) | 0.11(0.07 0.20) | 0.16(0.15 0.17) | 8.35(8.08 8.67) | 0.92(0.84 0.96) | |
MR ver | 8.73(2.93 13.19) | 0.12(0.06 0.20) | 0.04(0.03 0.06) | 21.1(17.43 26.59) | 0.92(0.89 0.96) | |
OR obl | -9.83(-13.15 -7.05) | 0.64(0.43 0.86) | 1.99(1.96 2.02) | |||
SR obl | -3.75(-7.76 -0.44) | 0.55(0.36 0.83) | 0.87(0.86 0.89) | 8.23(8.06 8.50) | 0.92(0.84 0.96) | |
MR obl | 8.53(3.27 12.69) | 0.52(0.26 0.81) | 0.18(0.11 0.32) | 24.36(18.39 28.90) | 0.92(0.84 0.96) | |
OR unip | -2.57(-5.83 -1.15) | 0.92(0.74 1.04) | 1.23(1.04 1.71) | |||
SR unip | 4.81(2.80 8.05) | 0.85(0.71 0.98) | 0.45(0.35 0.57) | 11.58(7.77 13.72) | 0.93(0.89 0.96) | |
MR unip | 6.79(5.05 10.87) | 0.84(0.69 0.96) | 0.36(0.24 0.45) | 13.79(9.20 16.91) | 0.96(0.92 0.96) |
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0009* | 0.0001* | 0.0043* |
SR ver vs MR ver | 0.0003* | 0.0000* | 0.0009* |
SR obl vs MR obl | 0.0008* | 0.0000* | 0.0000* |
SR unip vs MR unip | 0.0006* | 0.0000* | 0.0001* |
SR vs MR | 0.0000* | 0.0000* | 0.0000* |
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0000* | 0.0000* | 0.4514 |
SR ver vs MR ver | 0.0000* | 0.0000* | 0.2055 |
SR obl vs MR obl | 0.0000* | 0.0000* | 0.4115 |
SR unip vs MR unip | 0.0002* | 0.0001* | 0.8280 |
SR vs MR | 0.0000* | 0.0000* | 0.5800 |
SIR [dB] | Fetal Amp [µV] | matAmp [µV] | matAtt [dB] | QRSdetAcc | ||
Real dataset results | OR hor | -8.5(-12.09 -4.97) | 33.17(24.18 39.89) | 83.37(62.20 144.04) | ||
SR hor | -0.87(-7.39 2.23) | 32.14(24.61 36.42) | 28.97(23.00 69.61) | 15.02(9.11 21.50) | 0.62(0.50 0.84) | |
MR hor | 1.79(-1.20 5.17) | 30.61(25.83 37.10) | 24.75(13.71 32.91) | 25.75(19.80 33.41) | 0.85(0.77 0.94) | |
OR ver | -9.92(-12.79 -6.26) | 25.7(21.64 34.56) | 77.6(54.84 119.37) | |||
SR ver | -4.85(-8.91 -0.93) | 26.13(19.26 31.89) | 44.17(20.26 68.48) | 12.08(7.32 19.76) | 0.69(0.52 0.88) | |
MR ver | -0.06(-3.26 5.46) | 23.14(17.33 28.57) | 18.55(10.59 30.33) | 33.79(23.17 38.06) | 0.92(0.82 0.96) | |
OR obl | -13.05(-16.88 -5-76) | 38.45(29.91 46.66) | 142.47(74.90 246.37) | |||
SR obl | -5.48(-9.50 -0.39) | 34.81(24.95 42.67) | 60.68(33.25 107.82) | 13.99(7.88 20.71) | 0.61(0.52 0.84) | |
MR obl | 2.03(-2.78 4.92) | 33.46(24.63 43.78) | 27.38(17.92 40.94) | 35.09(26.38 41.31) | 0.89(0.77 0.92) | |
OR unip | -11.4(-13.72 -6.11) | 19.84(17.48 29.82) | 76.86(51.94 123.54) | |||
SR unip | -6.72(-8.60 -0.89) | 20.71(15.74 28.58) | 43.95(18.24 67.64) | 12.16(9.86 18.20) | 0.7(0.51 0.90) | |
MR unip | 2.63(-3.63 7.11) | 19.11(13.19 25.23) | 14.52(7.10 30.39) | 31.5(24.98 40.63) | 0.86(0.79 0.91) | |
Synthetic dataset results | OR hor | -12.8(-9.71 -15.84) | 0.63(0.44 0.90) | 2.78(2.75 2.81) | ||
SR hor | -7.32(-11.03 -4.59) | 0.51(0.33 0.70) | 1.18(1.16 1.19) | 8.57(8.46 8.78) | 0.9(0.82 0.96) | |
MR hor | 6.8(2.42 10.53) | 0.42(0.24 0.63) | 0.17(0.10 0.30) | 28.25(22.41 32.79) | 0.94(0.81 0.96) | |
OR ver | -8.61(-13.90 -4.50) | 0.14(0.08 0.21) | 0.37(0.37 0.38) | |||
SR ver | -2.8(-7.83 1.98) | 0.11(0.07 0.20) | 0.16(0.15 0.17) | 8.35(8.08 8.67) | 0.92(0.84 0.96) | |
MR ver | 8.73(2.93 13.19) | 0.12(0.06 0.20) | 0.04(0.03 0.06) | 21.1(17.43 26.59) | 0.92(0.89 0.96) | |
OR obl | -9.83(-13.15 -7.05) | 0.64(0.43 0.86) | 1.99(1.96 2.02) | |||
SR obl | -3.75(-7.76 -0.44) | 0.55(0.36 0.83) | 0.87(0.86 0.89) | 8.23(8.06 8.50) | 0.92(0.84 0.96) | |
MR obl | 8.53(3.27 12.69) | 0.52(0.26 0.81) | 0.18(0.11 0.32) | 24.36(18.39 28.90) | 0.92(0.84 0.96) | |
OR unip | -2.57(-5.83 -1.15) | 0.92(0.74 1.04) | 1.23(1.04 1.71) | |||
SR unip | 4.81(2.80 8.05) | 0.85(0.71 0.98) | 0.45(0.35 0.57) | 11.58(7.77 13.72) | 0.93(0.89 0.96) | |
MR unip | 6.79(5.05 10.87) | 0.84(0.69 0.96) | 0.36(0.24 0.45) | 13.79(9.20 16.91) | 0.96(0.92 0.96) |
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0009* | 0.0001* | 0.0043* |
SR ver vs MR ver | 0.0003* | 0.0000* | 0.0009* |
SR obl vs MR obl | 0.0008* | 0.0000* | 0.0000* |
SR unip vs MR unip | 0.0006* | 0.0000* | 0.0001* |
SR vs MR | 0.0000* | 0.0000* | 0.0000* |
SIR Results | Maternal Attenuation | Peak DetectorAccuracy | |
SR hor vs MR hor | 0.0000* | 0.0000* | 0.4514 |
SR ver vs MR ver | 0.0000* | 0.0000* | 0.2055 |
SR obl vs MR obl | 0.0000* | 0.0000* | 0.4115 |
SR unip vs MR unip | 0.0002* | 0.0001* | 0.8280 |
SR vs MR | 0.0000* | 0.0000* | 0.5800 |