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JSM Mathematics and Statistics

Fractional Stochastic Nonlinear Differential Equation Approach for Evolution in Time of Epidemiological Systems

Research Article | Open Access | Volume 7 | Issue 1
Article DOI :

  • 1. Federal Center for Technological Education of Minas Gerais, Brazil
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Corresponding Authors
Lima LS, Federal Center for Technological Education of Minas Gerais, Brazil
Abstract

The purpose of this paper is to develop the fractional stochastic nonlinear differential equation approach (FBM) to apply this in the study of the evolution in time of infected number by coronavirus in countries where the number of infected is large. The rises and falls of epidemiologic weeks of novel cases are treated as fractional white noise BH (t); 1/2 < H < 1, in the model for spreading of epidemiologic week of novel cases. Since the FBM approach provide a useful model for a host of natural time series presented by scientists, engineers and statisticians, we apply this formalism to study the spreading of coronavirus. Moreover, we use the rescaled range analysis (RS) to determine the Hurst index of the time series of epidemiologic weeks of novel cases which exhibits a Hurst index much larger than 1/2, what means that the time series has a very distinct behavior from a random walk or that the nth value of time series up time t 0 is independent of all the values before, t < t 0 .

Keywords

• Fractional Stochastic • Nonlinear Differential Equation • Hurst Index

Citation

Lima LS (2025) Fractional Stochastic Nonlinear Differential Equation Approach for Evolution in Time of Epidemiological Systems. JSM Math Stat 7(1): 1022.

INTRODUCTION

It is well known that FBMs can be employed to model the spread of infectious diseases, including COVID-19 [1-10]. These fractional noises also known as fractional Brownian motions incorporate both fractional calculus and stochastic elements, allowing the inclusion of long- range dependence and random fluctuations in the modeling process. However, the use of fractional calculus in epidemiology is a relatively advanced and specialized approach. The basic form of a fractional stochastic differential equation can be written as: dX(t) = aX(t)dt + bX(t)dBH (t), where X(t) represents the state variable (e.g., the number of infected individuals), the a and b are constants representing the deterministic and stochastic components, respectively, dt is the differential time increment, dBH (t) is the fractional Wiener process, of fractional order H where H ∈(1/2, 1).

The mathematical modeling for spreading of diseases has been per- formed since long time ago, where the model was known be given by dN/dt = aN3 + bN2 -cN, being the parameters a and b into the range a > 0 and 0 < a < b. Taking some randomness in these parameters, we get a more realistic model to treat real situations [11-16]. The purpose of this paper is to model the novel cases of epidemiologic weeks using the fractional white noise calculus approach. We analyze the rises and falls of novel cases of coronavirus reported by the public healthy agencies in countries as Brazil and India where the low number tests performed in the populations leads to a large uncertainty in the official data. Due to possibility that the dynamics of novel cases must exhibit long-range correlations thus, it mays be described in terms of long-memory processes [17].

The use of the standard stochastic calculus has been many employed in the literature for the study of the time behavior of time series of stock prices [16,18-21]. Moreover, the use of the stochastic differential equations that corresponds to the case H = 1/2, was used recently for us to study the spreading of coronavirus in Ref. [4]. Besides, the modeling based in the fractional stochastic differential equation has been used in [3,5-7]. The stochastic dynamics smoking with a non-Gaussian noise was studied in Refs. [22-24]. The dynamics of a stochastic COVID- 19 epidemic model with jump-diffusion, was analyzed in [22]. The stochastic susceptible-infected-recovered (SIR) dynamics expressed using the Itˆo calculus has been pro- posed in Refs. [25-31]. The statistical analysis described by the master equation and transition rates for the infection process was made in Ref. [32]. The statistical inference in the epidemic model for the Ebola virus was per- formed in [33]. The discrete-time epidemic model with binomial distribution has been used to study the trans- mission rate of covid in [34].

A statistical model for the health care impact of COVID-19 in India has been studied in [35]. Moreover, the effect of immunization through vaccination on the susceptible–infected–susceptible (SIS) epidemic spreading model was analyzed in [36]. Here, we propose the analysis based on the fractional Brownian motion to study the dynamics of epidemiologic weeks of novel cases of coronavirus. The plan of this paper is the following. In section II, we describe the fractional white noise analysis as a model for spreading epidemiological systems. In section III, we present the numerical results and the long range memory analysis, using the rescaled range (RS) analysis. In the last section IV, we present our conclusions and final remarks.

MODEL AND METHOD

The fractional Brownian motion (BMF) is defined as a family of Gaussian processes, being introduced by Kol- mogorov in [37], and indexed by the Hurst parameter H into the range 1/2 < H < 1. Being the first application made by Hurst in 1951 [38,39]. Such fractional Brownian motion was defined in Refs. [40, 41,42] where for each value of H, a real-valued Gaussian process BH (t), t ≤ 0 is defined by ⟨BH (t)⟩ = 0 and ⟨BH (t)BH (s)⟩ = the fractional Brownian motion is the standard Brownian motion or Wiener process. Moreover, we consider H restricted to range 1/2 < H < 1 and apply this as well as its modifier to model the infected number by coronavirus N (t) of epidemiologic weeks of novel cases. The model of spreading of novel cases N (t) is given by add of the least square fit g(t) to the logistic model with fractional noise which takes into account the isolation conditions and the vaccination of the population in each country, what has smoothing the curve of novel cases. Moreover, whether t → BH (t) is differentiable into the Schwartz space S(R) of rapidly decreasing smooth functions, being (SH )∗ His the dual of (S)H.

We have that the BH -integration theory of Eq. (1) is based on using of ordinary products path-wise and leads to an integral that for integrands g(t, ω) is defined where ?: a = t0 < t1 << tn = b is a partition of each interval [a, b] and ? = max0≤k≤n−1 (tk+1,tk ). These integrals do not have an expectation zero and are called fractional path-wise integrals. Here, we considerate the BH -integral considered in Ref. [43], defined by

Definition: Suppose g: R(S)∗ His a given function such that g(t) WH (t) is integrable in (S)∗ H. Then we definite the fractional stochastic integral of Itˆo type, by

Where ? denotes the Wick’s product [40-47]. These integrals that use the Wick’s product are known as fractional Itˆo integrals with reference to corresponding situation of standard Brownian motion [41,42]. Due to the behavior of novel cases, we consider the deterministic part adjusting to the data of epidemiologic weeks of novel cases using a suave curve. The aim is simply provide a smoothed version of the time series using standard methods as the lowest regression. Furthermore, we aim to calculate the ensemble of all possible trajectories using the fractional behavior into the range of large t values reflects in an increase of the uncertainty in the official data and to the low-number of test performed in the populations. For modeling of the zigzag behavior of novel cases, we add a random noise term in the logistic model for spreading of infectious number as given by Eq. (1) in order to simulate the effect of rises and falls of novel cases [4]. We have that comes from the least squares Fit to the set of data into the period considered. The case a ? 0.017, b ? 0.26 and c ? 0.13 and without randomness (Γ = 0,) corresponds to the very known logistic model for the small- pox. Moreover, the daily fluctuations with a weekly cycle of reported cases have been observed in many countries and are due to the diagnostic and data reporting practices [48].

RESULTS AND DISCUSSION

We write the BMF model that is a Gaussian pro- cess WH (t), t > 0 with zero mean and stationary in crements and variance given by W 2 (t) = t2H . The sample path of the BMF model is a fractal curve with fractal dimension d = 1/H, where H = 1/2 corresponds to the standard Brownian motion whose incre- ments ?WH (t) = WH (t + 1) WH (t) are statistically independent. For H = 1/2 the increments ?WH (t) are known as fractional white noise, showing long-range correlation as ⟨?WH (t + h)?WH (t)⟩ ? 2H(2H − 1)h2H−2, for h → ∞. For H ∈ (1/2, 1) the increments are positively correlated exhibiting thus a persistent behavior. For H ∈ (0, 1/2), the increments are negatively correlated, showing anti-persistence. For H = 1/2, we write the Wiener increment as dWH(t) ∼ where RG is an aleatory generator number with Gaussian distribution of mean zero and variance. In following, we write the Eq. (1) in the discrete form with the time step ?t used in the simulations as ?t = 0.1, with t running along chosen units (say seconds, minutes, days or weeks). In Figure 1, we present the simulation of the model Eq. (1 for a particular set of values of parameters a, b, c and Γ(N (t), t). In (a) we plot the epidemiologic week of novel cases reported in Brazil.

Figure 1 Simulation of the model Eq. (1 for the particular set of values of parameters a, b, c and Γ (N (t), t). (a) Data of epidemiologic week of novel cases reported in Brazil in 2023 year. (b) The time series of the model Eq. (1), for values of Hurst exponent: H = 1/2. The red-square line are the epidemiologic week of novel cases reported and the blackline is the result of the simulation of the model for set of parameters a = b = c = 0 and Γ = g

In plot (b), We plot the time series of model Eq. (1) for the value of Hurst parameter as H = 1/2. The red-square line are the data of epidemiologic week of novel cases reported and the black-line is the result of the simulation of the model for set of parameters a = b = c = 0 and Γ = g. In Figure 2, we perform simulations of the model Eq. (1 for H = 1/2 and Γ = g and different values of (a, b, c). (a) We plot the time series for the values of (a, b, c) such as (a, b, c) = (1.0, 2.0, 1.0) x10−10 (red-circle-line), (a, b, c) = (5.0, 10.0, 5.0) 10−10 (green-square-line), (a, b, c) = (5.0, 10.0, 5.0)x10−9 (blue-triangle-up-line). In plot (b) we present the behavior for values of pa- rameters a, b, c and for (a, b, c) = (0, 0, 0), that is represented as magenta-line: (a, b, c) = (1.0, 2.0, 1.0) x 10−10 (red-line), (a, b, c) = (5.0, 10.0, 5.0) x 10−10 (greenline), (a, b, c) = (5.0, 10.0, 5.0) x10−9 (blue-line). For a, b, c, we have that the drift term of the model above is given by a polynomial of third order in Nt . In general, a point N0 ∈ R in the model Eq. (1) is called a regular point if is locally integrable, L1loc(N0 ) and hence

Figure 2 Simulation of the model Eq. (1 for H = 1/2 and Γ = g. (a) We plot the time series for different values of (a, b, c) parameters such as (a, b, c) = (1.0, 2.0, 1.0) × 10−10 (red-circle-line), (a, b, c) = (5.0, 10.0, 5.0) × 10−10 (green-square-line), (a, b, c) = (5.0, 10.0, 5.0) × 10−9 (blue-triangle- up-line)and H = 1/2. (b) Behavior for different values of pa- rameters a, b, c. (a, b, c) = (0, 0, 0) mangueta-line, (a, b, c) = (1.0, 2.0, 1.0) × 10−10 (red-line), (a, b, c) = (5.0, 10.0, 5.0) ×10−10 (green-line), (a, b, c) = (5.0, 10.0, 5.0)×10−9 (blue-line).

then there exist a unique solution for the model above, Eq. (1). The behavior of the solution at + and singularities is discussed in Ref. [49]. In Figure 3, we per- form simulations of the model Eq. (1). We plot the time series for different values of Hurst index H. We con- sider the set of parameters (a, b, c) such as (a, b, c) = (1.0, 2.0, 1.0) x10−10. We get that the model fits better when (a, b, c) = (1.0, 2.0, 1.0) x 10−10 and the value of the Hurt index is close to H = 1, that is in accordance with the value of the Hurst index obtained by rescaled range method H1 for the time series of epidemiologic weeks data.

Figure 3 Simulation of the model Eq. (1) for different values of H and Γ = g. (a) We plot the time series for different values of Hurst index H. We consider the set of parameters (a, b, c) such as (a, b, c) = (1.0, 2.0, 1.0) × 10−10. The red-solid-line correspond to the data of epidemiologic weeks of novel cases reported in Brazil in (2023).

RS ANALYSIS

There are several estimators for the Hurst exponent such as rescaled range (RS) analysis, multifractal and detrended fluctuation analysis [50,51] that differ basically by the choice of the fluctuation measure. In Figure 4, we present the Log-Log graphic with objective to determine the Hurst index. We use the RS analysis, where the Hurst exponent is directly obtained and it is used as a measure of long-term memory of time series. It relates with the autocorrelations of the time series and the rate in which this decrease as the lag between pairs of values increases. The start point of the method is to determine the standard deviation using the mean field approach as and the range Rt of the series where H is the Hurst index. We get the value of the Hurst exponent using the RS method for time series of epidemiologic weeks of novel cases as H = 1.166(5). The numerical results display a Hurst index close to H = 1, being very far from the value for the standard Brownian motion H = 1/2. In spite of the constant value H ~1.17 obtained into the range considered, in a real situation, we must have a time dependent H = H(t) that is, the estimator is relevant into the current context and must be time dependent. The value found for the data set indicates thus, a strongly persistent behavior for the time series N (t) of epidemiologic week of novel cases reported.

OUTLOOK

In brief, we have analyzed the behavior of novel cases of epidemiologic weeks of coronavirus using the fractional white noise calculus, with the aim to model the rises and falls of these. We get that the model with H~1 fits better to the set of data reported. This value is closer to the value obtained for the time series using the RS method. The variability in the time series for instance is mostly due to the case numbers reports not being filled on weekends, leading to a large-amplitude oscillation in the data. Moreover, due to the large uncertainty in the official case numbers reported which is a consequence of the low number of tests performed in the population and to underreporting, we have a large uncertainly in the results divulged what becomes necessary the addition of random terms in the equations that model the time evolution of infected numbers.

We get a Hurst index close to H~1.17 for the time series of epidemiological weeks indicating so, a large deviation from the result H = ½ which corresponds to the standard stochastic calculus. An additional analysis whether fractional Gaussian noise is the best phenomenological approach to the fluctuations of coronavirus data can be made in a future work. The starting point could be to implement schemes as detrended fluctuation analysis, with possible free parameters, and a larger database that is, coronavirus data from many countries. Nevertheless, we must be careful in using of BMF and Gaussian noise with algebraic correlations for further investigation of data-driven what correlation structure the fluctuations display across different data sets.

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Lima LS (2025) Fractional Stochastic Nonlinear Differential Equation Approach for Evolution in Time of Epidemiological Systems. JSM Math Stat 7(1): 1022.

Received : 25 Jun 2025
Accepted : 24 Jun 2025
Published : 25 Jun 2025
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Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
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