
Since the COVID-19 epidemic, mathematical and simulation models have been extensively utilized to forecast the virus's progress. In order to more accurately describe the actual circumstance surrounding the asymptomatic transmission of COVID-19 in urban areas, this research proposes a model called Susceptible-Exposure-Infected-Asymptomatic-Recovered-Quarantine in a small-world network. In addition, we coupled the epidemic model with the Logistic growth model to simplify the process of setting model parameters. The model was assessed through experiments and comparisons. Simulation results were analyzed to explore the main factors affecting the spread of the epidemic, and statistical analysis that was applied to assess the model's accuracy. The results are consistent well with epidemic data from Shanghai, China in 2022. The model can not only replicate the real virus transmission data, but also anticipate the development trend of the epidemic based on available data, so that health policy-makers can better understand the spread of the epidemic.
Citation: Qinghua Liu, Siyu Yuan, Xinsheng Wang. A SEIARQ model combine with Logistic to predict COVID-19 within small-world networks[J]. Mathematical Biosciences and Engineering, 2023, 20(2): 4006-4017. doi: 10.3934/mbe.2023187
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Since the COVID-19 epidemic, mathematical and simulation models have been extensively utilized to forecast the virus's progress. In order to more accurately describe the actual circumstance surrounding the asymptomatic transmission of COVID-19 in urban areas, this research proposes a model called Susceptible-Exposure-Infected-Asymptomatic-Recovered-Quarantine in a small-world network. In addition, we coupled the epidemic model with the Logistic growth model to simplify the process of setting model parameters. The model was assessed through experiments and comparisons. Simulation results were analyzed to explore the main factors affecting the spread of the epidemic, and statistical analysis that was applied to assess the model's accuracy. The results are consistent well with epidemic data from Shanghai, China in 2022. The model can not only replicate the real virus transmission data, but also anticipate the development trend of the epidemic based on available data, so that health policy-makers can better understand the spread of the epidemic.
The COVID-19 epidemic is still significantly affecting our lives today. Worldwide, there are still sporadic, and as viruses evolve, more novel coronavirus strains are emerging, and their infectiousness is growing. Even if the majority of people are currently vaccinated, the infection cannot be completely prevented. We need to be prepared to coexist with viruses for a long period.
In actuality, this is not the first time in human history that an epidemic has spread widely. Disastrous epidemics such as SARS and H1N1 had also seriously harmed humanity. To predict how infectious diseases spread in human society, many models have been proposed to model epidemic transmission patterns, such as Susceptible-Infective (SI) [1], Susceptible-Infective-Recovered (SIR) [2], Susceptible-Infective-Susceptible (SIS) [3], and Susceptible-Exposed-Infective-Recovered (SEIR) [4]. Researchers have also suggested other derivative models in addition to these fundamental simple models, which are distinguished by an incubation period. Robert A Brown proposed the SIARQ model, a simple model for controlling COVID-19 infection in urban campuses and studied the spread of campus epidemics with asymptomatic patients as the main source of infection [5]. Liu et al presented an adaptive SEIARD model with internal source and isolation intervention to simulate the effects of changing behavior of the SARS-COV-2 in the US [6]. These studies were mainly based on modeling the different states of patients in the course of the disease, the majority of them used an epidemiological model and did not consider the social network in real life.
In 1998, Watts and Strogatz proposed a small-world network (SW) [7], a network between random and regular networks. This kind of network randomizes the node connections with probability p, and the resulting system can not only have a high degree of aggregation like a regular network, but also have a small characteristic path length like a random network. SW has been shown to exist in many interactive networks, including social networks [8]. And, there have been many cases of modeling infectious diseases using a small-world network. For example, Liu and Xiao used differential equations and Routh-Hurwiz theory to prove two different models based on SW networks, SEIRS and SEIQRS [9]. A SEIR-SW model based on graph theory was proposed by Younsi et al. [10]. Saramäki and Kaski proposed a dynamic small-world network-based SIR model to analyze the spread of random infectious diseases [11]. Compared with traditional compartment models, these models take into account the influence of social networks, making the spread of infectious diseases more in line with the actual situation. But, the models have too many parameters, which makes parameter adjustment extremely complicated. And, many key parameters mainly refer to previous research results or manual adjustments.
In this study, we simulate and evaluate the large-scale Omicron virus outbreak in Shanghai using an infectious disease model (SEIARQ) based on small-world networks. Additionally, we combined the Logistic growth model with the SEIARQ model to simulate and optimize it. This increased the model's accuracy while minimizing the need for labor-intensive parameter adjustments, making the model simpler to use.
The remainder of the paper is organized as follows. Section 2 presents the SEIARQ model considering the small-world network effect. Section 3 introduces the Logistic growth model and explains how to combine SEIARQ with the Logistic growth model. Section 4 shows the simulations and discussions. Finally, Section 5 presents the conclusions.
At present, the Omicron virus shows high infectivity and low toxicity. Most of the infected people have no symptoms, but they are still contagious [12]. It can also be seen from Figure 1 that number of asymptomatic patients is significantly larger than confirmed patients. At the same time, with the intervention of the government, patients detected by nucleic acid testing will be sent to treatment or isolation, and close contacts will also be required to self-isolate, cutting off the transmission route of the virus to a certain extent. In addition, owing to the higher-frequency nucleic acid testing and immediate isolation measure in China, the number of people being quarantined also need to be considered. Therefore, we divide the population in the small-world network into six parts, assuming that the impact of the number of deaths on the network is negligible, and that the infected persons become immune and will not be reinfected after recovering. In order to model social contacts among human populations, we can construct a small-world network by representing individuals as nodes and social relationships as edges [10]. In this paper, we used the average degree distribution k to represent the connection of the network, which means that each node in the network has an average of k neighbors. If the node is infected, it will infect k neighbors with a certain probability. The schematic of the model is shown in Figure 2.
According to the mean-field theory, the mean field equations of the epidemic spread in the small-world network are:
dS(t)dt=−β1<k1>S(t)I(t)N−β2<k2>S(t)A(t)N | (1) |
dE(t)dt=β1<k1>S(t)I(t)N+β2<k2>S(t)A(t)N−(p1+p2)E(t) | (2) |
dI(t)dt=p1E(t)−δ1I(t)−(1−δ1)γ1I(t) | (3) |
dA(t)dt=p2E(t)−δ2A(t)−(1−δ2)γ2A(t) | (4) |
dQ(t)dt=δ1I(t)+δ2A(t)−γQ(t) | (5) |
dR(t)dt=(1−δ1)γ1I(t)+(1−δ2)γ2A(t)+γQ(t) | (6) |
The meaning of each parameter of the model is as Table 1:
Parameters | Meaning |
N | size of small world network |
S(t) | number of susceptible people |
E(t) | number of exposed people |
I(t) | number of infected people |
A(t) | number of asymptomatic people |
R(t) | number of recovered people |
Q(t) | number of quarantine people |
β1 | propagation coefficient of the infected people |
β2 | propagation coefficient of the asymptomatic people |
k1, k2 | average degree distribution of small world network |
p1 | proportion of exposed people converted to infected people |
p2 | proportion of exposed people converted to asymptomatic people |
δ1 | isolation rate of infected people |
δ2 | isolation rate of asymptomatic people |
γ1,γ2,γ | recovered rate |
In the infectious disease dynamics model, the basic reproduction number R0 is a very important parameter, which represents the number of people infected by a patient in an average disease cycle in a disease-free equilibrium (DFE) state. R0 is a marker that determines whether a virus is prevalent. The calculation of R0 has guiding significance for disease prevention and control strategies. R0 is also a threshold number of the model, if R0 < 1, the DFE is local asymptotically stable, and the disease cannot invade the population, but if R0 > 1, then the DFE is unstable and invasion is always possible [13].
According to the next-generation matrix method, R0 is obtained by calculating the spectral radius of the reproduction matrix [14,15].
First, the variables are divided into two categories: infection class-{E(t), I(t), A(t), Q(t)}, non-infection class {S(t), R(t)}. Then, let Fi be the rate of newly infected individuals in group i, Vi=V−i−V+ibe the transfer rate, V−i be the rate of individuals removed from group i, and V+i be moved into group i by any means other than infection ratio of individuals. It can be obtained from formula Eqs (1)–(6) that
FEIAQ=[β1<k1>S(t)I(t)N+β2<k2>S(t)A(t)N000] | (7) |
VEIAQ=[(p1+p2)E(t)δ1I(t)+(1−δ1)γI(t)−p1E(t)δ2A(t)+(1−δ2)γA(t)−p2E(t)γQ(t)−δ1I(t)−δ2A(t)] | (8) |
Let F = [∂Fi∂xi(x0)], V = [∂Vi∂xi(x0)], x0 is the disease-free equilibrium point. Thus, we get
F=(E,I,A,Q)=Jacobian(FEIAQ)=[0000β1<k1>S(t)N000β2<k2>S(t)N0000000]T | (9) |
V(E,I,A,Q)=Jacobian(VEIAQ)=[p1+p2000−p1δ1+(1−δ1)γ00−p20δ2+(1−δ2)γ00−δ1−δ2γ] | (10) |
FV−1=[p1β1<k1>S(t)N(p1+p2)(δ1+(1−δ1)γ)+p2β2<k2>S(t)N(p1+p2)(δ2+(1−δ2)γ)000β1<k1>S(t)N(δ1+(1−δ1)γ)000β2<k2>S(t)N(δ2+(1−δ2)γ)0000000]T | (11) |
Let the right-hand side of the differential equation system be 0, and I = 0, A = 0, it is easy to get the disease-free equilibrium point E0 = (N (0), 0, 0, 0, 0, 0), and find it at the disease-free equilibrium point
R0=ρ(FV−1)=p1β1<k1>(p1+p2)(δ1+(1−δ1)γ)+p2β2<k2>(p1+p2)(δ2+(1−δ2)γ) | (12) |
From Eq (12), it can be found that the spread threshold of the epidemic depends on some key parameters. R0 is positively correlated with the average degree distribution of the small-world network and the infection rate, and negatively correlated with the isolation rate, which is the same as our perception.
The logistic equation is a well-known population growth model proposed by mathematical biologist Pierre Francois Verhulst, which is widely used in population growth and forecasting [16]. The model is represented by the following differential equation:
dNdt=rN(1−NK) | (13) |
The solution to the equation is
N(t)=K1+(KN0−1)e−rt | (14) |
Among them, K is the environmental capacity, representing the maximum cumulative number of infected people in the infectious disease model; N0 is the initial value of the population, representing the initial number of infected people in the infectious disease model; r is the infection rate in the infectious disease model; t is time, N(t) is the population number that changes over time, representing the cumulative number of infected people changing over time in the infectious disease model.
In the case of known parameters K, N0, r, the logistic growth model can be used to predict infectious diseases, for example, Morsi and Alzahrani [17] used logistic growth model for the complex spread of COVID-19 and forecasted future values in Australia and Brazil within a time interval of six days, but since the model is monotonically increasing, it can only predict the cumulative number of infected people, but not the existing confirmed number of people. The SEIARQ model can predict the number of confirmed daily diagnoses, and can also obtain the turning point of infectious diseases, but due to plenty of model parameters, the task of adjustment will be particularly difficult. Although the forms of the two models are quite different, when describing the same type of infectious disease, because the characteristics of the infectious disease and the environment are the same, the parameters of the two models can be interchanged, which is also verified in subsequent simulation tests. Therefore, consider combining the Logistic with SEIARQ.
The specific idea is as follows:
1) Using actual data of infected and asymptomatic to fit Logistic equation, and getting parameters of Logistic equation.
2) Assume N0 in the Logistic growth model to be the initial number of infections (A0 or I0) in the SEIARQ model and r as the infection rate β in the SEIARQ model. Multiply the environmental capacity K by ε (ε > 1) to estimate the size of the small world network and the initial number of susceptible populations in the SEIARQ model S0. p is determined by the environmental capacity obtained from the infected and asymptomatic fits. Assume that there is no person exposed, recovered or isolated at the beginning of transmission, so E0, R0 and Q0 are 0.
3) Initialize the remaining parameters of the model and use the model to make predictions and compare to the true value.
We conducted experiments to examine the proposed SEIARQ model. The statistics used in this paper is the daily epidemic data from Shanghai, China since February 2022 [18]. To fit the Logistic growth model, it is necessary to divide the entire dataset into training set and test set. In this paper, the training set represents the known epidemic data used for logistic model parameter fitting, and the test set represents the known epidemic data used to compare with the SEIARQ model. Here we limited the training set from February 27th, 2022 to April 21st, 2022 and used the following 7 days to predict. In the experiments, we employed the grid search approach and the nonlinear least squares method to fit the Logistic growth model's parameters. The parameter values obtained by fitting the logistic growth model and the estimated values of the remaining parameters are shown in the following Table 2:
Parameters | Value | Source |
S0,I0,A0, E0,R0,Q0 | 716800, 0, 33, 0, 0, 0 | Fit |
β1, β2 | 0.23, 0.22 | Fit |
k1,k2 | 10, 10 | Estimate |
p1,p2 | 0.0145, 0.1283 | Fit |
δ1,δ2 | 0.7, 0.62 | Estimate |
γ1,γ2,γ | 0.1, 0.1, 0.1 | Ref [19] |
All experiments are run on Microsoft Windows 10, the computer hardware environment is Intel(R) Core (TM) i5-9300H CPU 2.40 GHz with 12GB RAM, the Interpreter is Python 3.10.
The numerical simulation results of the model are shown in Figure 3. The 7-day forecast results are compared with the actual results as shown in Table 3. Please note that the data compared in Table 3 are the total number of cases, including confirmed and asymptomatic.
Date | Real value | Predict value | Relative error |
4-22 | 23370 | 19475 | 16.67% |
4-23 | 21058 | 17908 | 14.96% |
4-24 | 19455 | 16390 | 15.75% |
4-25 | 16980 | 14939 | 12.02% |
4-26 | 13562 | 13569 | 0.05% |
4-27 | 10622 | 12289 | 15.69% |
4-28 | 15032 | 11100 | 26.16% |
It can be seen that due to changes in local epidemic prevention policies and other external factors, the model parameters are not fully applicable to all stages of the epidemic development, resulting in a gap between the predicted value and the actual value, but the predicted curve of the model and the actual epidemic situation curves are still highly similar.
Here we use mean absolute percentage error (MAPE) and root mean squared percentage error (RMSPE) to evaluate the performance of the model, and compare it with the result of the Shanghai epidemic prediction model in Ref [19]. When error ≥ 50%, the model is poor, 20% ≤ error < 50% is reasonable, 10% ≤ error < 20% is good, and error < 10% is accurate. MAPE and RMSPE is define as follows:
MAPE=1n∑ni=1|yi−^yiyi|×100% | (15) |
RMSPE=√∑ni=1(yi−^yiyi)2n×100% | (16) |
where ^yi represents the predicted value of the model on the i-th day, yi represents the true value on the i-th day, and ¯yi represents the average value on the ith day. The results are shown in Table 4 as follow:
Variable | MAPE of our model | RMSPE of our model | MAPE of Ref [19] | RMSPE of Ref [19] | Performance |
Newly confirmed cases | 27.98% | 36.50% | 33.86% | 37.01% | Reasonable |
Newly asymptomatic infectious | 14.47% | 16.14% | 12.34% | 16.45% | good |
Newly total cases | 11.97% | 13.37% | / | / | good |
We further investigate the impact of the parameters that need to be tuned on the prediction performance of the model. Among them, the average degree distribution and recovery rate can be found in the literature and are relatively easy to debug. The isolation rate needs to be adjusted manually. Therefore, the impact of the isolation rate on the prediction effect of the model is mainly analyzed. It can be seen from the Figure 4 that increasing the isolation and reducing the average degree distribution can significantly inhibit the spread of the epidemic. When the isolation rate is 0, the model degenerates into the SEIAR model, and the entire prediction curve is very different from the actual value, so the introduction of isolation is necessary for epidemic prediction.
The COVID-19 is the largest worldwide epidemic that people have encountered in the last 100 years. The coronavirus causes daily infections or fatalities in humans. On September 1, there were more than 600 million confirmed cases worldwide, and there had been more than 6 million fatalities [20]. Modeling and analysis of the epidemic can help policymakers understand the development trend of the epidemic to formulate effective policies to control the epidemic.
This paper mainly proposes the SEIARQ model under the small world network for the new virus-mystery clone, and combines the Logistic growth model in the numerical simulation process to improve the simulation efficiency and reduce the number of parameters to be adjusted to 3 categories (average degree distribution, isolation rate, recovered rate), which significantly reduces the complexity of parameter adjustment. Additionally, we performed a thorough examination of the model and calculated the fundamental reproduction number. The results of the calculations demonstrate that just a few important factors are relevant to the model's propagation threshold. The model's outcomes in the numerical simulation analysis are favorable. When the actual adjustment parameters are only 3, the error of the asymptomatic patients is close to 10%, the error of the confirm infectious is about 30%, and the error of the total number of patients is close to 10%, which is almost the same as the result of Ref [19]. In the contrast, Ref [19] has 10 estimated parameters. Experimental results also show that control the average degree distribution in the small world can be effectively to curb the development of the epidemic in SEIAQR model, which means weaker contact between people will slow down the spread of the epidemic.
Also, the model has several restrictions. We did not take mortality and secondary illnesses into account. Additionally, the isolation rate may alter as a result of modifications to local laws and nucleic acid testing, causing inconsistencies between the model and the real curve at specific phases. Long-term forecasts are not guaranteed to be accurate throughout our simulation, which is a drawback that most models cannot avoid.
The authors declare there is no conflict of interest.
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1. | Harrison Huang, Shan Su, Lu Li, Advancing timber construction: historical growth, research frontiers, and time series forecasting, 2024, 1346-7581, 1, 10.1080/13467581.2024.2373829 | |
2. | Liangjian Hu, Meisong Shi, Meili Li, Junling Ma, Junyuan Yang, The effectiveness of control measures during the 2022 COVID-19 outbreak in Shanghai, China, 2023, 18, 1932-6203, e0285937, 10.1371/journal.pone.0285937 |
Parameters | Meaning |
N | size of small world network |
S(t) | number of susceptible people |
E(t) | number of exposed people |
I(t) | number of infected people |
A(t) | number of asymptomatic people |
R(t) | number of recovered people |
Q(t) | number of quarantine people |
β1 | propagation coefficient of the infected people |
β2 | propagation coefficient of the asymptomatic people |
k1, k2 | average degree distribution of small world network |
p1 | proportion of exposed people converted to infected people |
p2 | proportion of exposed people converted to asymptomatic people |
δ1 | isolation rate of infected people |
δ2 | isolation rate of asymptomatic people |
γ1,γ2,γ | recovered rate |
Parameters | Value | Source |
S0,I0,A0, E0,R0,Q0 | 716800, 0, 33, 0, 0, 0 | Fit |
β1, β2 | 0.23, 0.22 | Fit |
k1,k2 | 10, 10 | Estimate |
p1,p2 | 0.0145, 0.1283 | Fit |
δ1,δ2 | 0.7, 0.62 | Estimate |
γ1,γ2,γ | 0.1, 0.1, 0.1 | Ref [19] |
Date | Real value | Predict value | Relative error |
4-22 | 23370 | 19475 | 16.67% |
4-23 | 21058 | 17908 | 14.96% |
4-24 | 19455 | 16390 | 15.75% |
4-25 | 16980 | 14939 | 12.02% |
4-26 | 13562 | 13569 | 0.05% |
4-27 | 10622 | 12289 | 15.69% |
4-28 | 15032 | 11100 | 26.16% |
Parameters | Meaning |
N | size of small world network |
S(t) | number of susceptible people |
E(t) | number of exposed people |
I(t) | number of infected people |
A(t) | number of asymptomatic people |
R(t) | number of recovered people |
Q(t) | number of quarantine people |
β1 | propagation coefficient of the infected people |
β2 | propagation coefficient of the asymptomatic people |
k1, k2 | average degree distribution of small world network |
p1 | proportion of exposed people converted to infected people |
p2 | proportion of exposed people converted to asymptomatic people |
δ1 | isolation rate of infected people |
δ2 | isolation rate of asymptomatic people |
γ1,γ2,γ | recovered rate |
Parameters | Value | Source |
S0,I0,A0, E0,R0,Q0 | 716800, 0, 33, 0, 0, 0 | Fit |
β1, β2 | 0.23, 0.22 | Fit |
k1,k2 | 10, 10 | Estimate |
p1,p2 | 0.0145, 0.1283 | Fit |
δ1,δ2 | 0.7, 0.62 | Estimate |
γ1,γ2,γ | 0.1, 0.1, 0.1 | Ref [19] |
Date | Real value | Predict value | Relative error |
4-22 | 23370 | 19475 | 16.67% |
4-23 | 21058 | 17908 | 14.96% |
4-24 | 19455 | 16390 | 15.75% |
4-25 | 16980 | 14939 | 12.02% |
4-26 | 13562 | 13569 | 0.05% |
4-27 | 10622 | 12289 | 15.69% |
4-28 | 15032 | 11100 | 26.16% |
Variable | MAPE of our model | RMSPE of our model | MAPE of Ref [19] | RMSPE of Ref [19] | Performance |
Newly confirmed cases | 27.98% | 36.50% | 33.86% | 37.01% | Reasonable |
Newly asymptomatic infectious | 14.47% | 16.14% | 12.34% | 16.45% | good |
Newly total cases | 11.97% | 13.37% | / | / | good |