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首页> 外文期刊>International Journal of Genomics >A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis
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A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis

机译:机械的随机模型有助于理解多发性硬化症的病程和发病机理

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摘要

Heritable and nonheritable factors play a role in multiple sclerosis, but their effect size appears too small, explaining relatively little about disease etiology. Assuming that the factors that trigger the onset of the disease are, to some extent, also those that generate its remissions and relapses, we attempted to model the erratic behaviour of the disease course as observed on a dataset containing the time series of relapses and remissions of 70 patients free of disease-modifying therapies. We show that relapses and remissions follow exponential decaying distributions, excluding periodic recurrences and confirming that relapses manifest randomly in time. It is found that a mechanistic model with a random forcing describes in a satisfactory manner the occurrence of relapses and remissions, and the differences in the length of time spent in each one of the two states. This model may describe how interactions between “soft” etiologic factors occasionally reach the disease threshold thanks to comparably small external random perturbations. The model offers a new context to rethink key problems such as “missing heritability” and “hidden environmental structure” in the etiology of complex traits.
机译:遗传和非遗传因素在多发性硬化症中起作用,但是它们的作用大小似乎太小,对疾病病因学的解释相对较少。假设触发疾病发作的因素在一定程度上也是引起疾病缓解和复发的因素,我们试图对包含疾病复发和缓解时间序列的数据集进行观察,对疾病进程的不稳定行为进行建模70位患者没有任何可改善疾病的疗法。我们显示,复发和缓解遵循指数衰减分布,不包括周期性复发并确认复发随时间随机出现。发现具有随机强迫的机械模型以令人满意的方式描述了复发和缓解的发生以及在两种状态的每一种中花费的时间长度的差异。该模型可以描述由于相对较小的外部随机扰动,“软”病因之间的相互作用如何偶尔达到疾病阈值。该模型为重新思考关键性问题(例如复杂性状的病因学)中的“缺失遗传性”和“隐藏环境结构”提供了新的环境。

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