Key result
Mechanistic Markov model links subclinical atherosclerosis to MI, revealing postmenopausal shifts in female disease dynamics.
Why the study?
Analyzing epidemiological data with simplified mathematical models links incidence to biological processes, and solving models solely by simulation provides considerable modeling flexibility.
A unified mathematical simulation model can effectively link the biological progression of early subclinical atherosclerosis to population-level myocardial infarction incidence.
Highlights potential menopause-driven atherosclerosis acceleration; leaves open causal validation and targeted prevention trials in perimenopausal women.
Analyzing epidemiological data with simplified mathematical models of disease development provides a link between the time-course of incidence and the underlying biological processes. Here we point out that considerable modeling flexibility is gained if the model is solved by simulation only. To this aim, a model of atherosclerosis is proposed: a Markov Chain with continuous state space which represents the coronary artery intimal surface area involved with atherosclerotic lesions of increasing severity. Myocardial infarction rates are assumed to be proportional to the area of most severe lesions. The model can be fitted simultaneously to infarction incidence rates observed in the KORA registry, and to the age-dependent prevalence and extent of atherosclerotic lesions in the PDAY study. Moreover, the simulation approach allows for non-linear transition rates, and to consider at the same time randomness and inter-individual heterogeneity. Interestingly, the fit revealed significant age dependence of parameters in females around the age of menopause, qualitatively reproducing the known vascular effects of female sex hormones. For males, the incidence curve flattens for higher ages. According to the model, frailty explains this flattening only partially, and saturation of the disease process plays also an important role. This study shows the feasibility of simulating subclinical and epidemiological data with the same mathematical model. The approach is very general and may be extended to investigate the effects of risk factors or interventions. Moreover, it offers an interface to integrate quantitative individual health data as assessed, for example, by imaging.
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Simonetto et al. (2021) studied Atherosclerosis and Myocardial Infarction (n=449,227). Mathematical modeling of atherosclerosis vs. Descriptive parametric models was evaluated on Model fit (deviance) to myocardial infarction incidence rates and age-dependent atherosclerotic lesions. A mechanistic Markov chain model successfully fitted subclinical atherosclerosis data and epidemiological myocardial infarction incidence simultaneously, revealing significant age-dependent parameter shifts in females around menopause.
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