Dynamic model assuming mutually inhibitory biomarkers of frailty suggests bistability with contrasting mobility phenotypes.

Frontiers in network physiology Pub Date : 2023-05-04 eCollection Date: 2023-01-01 DOI:10.3389/fnetp.2023.1079070
Nathan Schaumburger, Joel Pally, Ion I Moraru, Jatupol Kositsawat, George A Kuchel, Michael L Blinov
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Abstract

Bistability is a fundamental biological phenomenon associated with "switch-like" behavior reflecting the capacity of a system to exist in either of two stable states. It plays a role in gene regulation, cell fate switch, signal transduction and cell oscillation, with relevance for cognition, hearing, vision, sleep, gait and voiding. Here we consider a potential role for bistability in the existence of specific frailty states or phenotypes as part of disablement pathways. We use mathematical modeling with two frailty biomarkers (insulin growth factor-1, IGF-1 and interleukin-6, IL-6), which mutually inhibit each other. In our model, we demonstrate that small variations around critical IGF-1 or IL-6 blood levels lead to strikingly different mobility outcomes. We employ deterministic modeling of mobility outcomes, calculating the average trends in population health. Our model predicts the bistability of clinical outcomes: the deterministically-computed likelihood of an individual remaining mobile, becoming less mobile, or dying over time either increases to almost 100% or decreases to almost zero. Contrary to statistical models that attempt to estimate the likelihood of final outcomes based on probabilities and correlations, our model predicts functional outcomes over time based on specific hypothesized molecular mechanisms. Instead of estimating probabilities based on stochastic distributions and arbitrary priors, we deterministically simulate model outcomes over a wide range of physiological parameter values within experimentally derived boundaries. Our study is "a proof of principle" as it is based on a major assumption about mutual inhibition of pathways that is oversimplified. However, by making such an assumption, interesting effects can be described qualitatively. As our understanding of molecular mechanisms involved in aging deepens, we believe that such modeling will not only lead to more accurate predictions, but also help move the field from using mostly studies of associations to mechanistically guided approaches.

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假设相互抑制的虚弱生物标志物的动态模型表明,双稳态具有截然不同的流动性表型。
双稳态是一种基本的生物现象,与 "开关样 "行为有关,反映了系统在两种稳定状态中任选其一的能力。它在基因调控、细胞命运转换、信号转导和细胞振荡中发挥作用,并与认知、听觉、视觉、睡眠、步态和排尿有关。在此,我们考虑了双稳态性在特定衰弱状态或表型的存在中的潜在作用,作为失能途径的一部分。我们使用数学模型对两种相互抑制的虚弱生物标志物(胰岛素生长因子-1(IGF-1)和白细胞介素-6(IL-6))进行分析。在我们的模型中,我们证明了临界 IGF-1 或 IL-6 血液水平的微小变化会导致截然不同的活动能力结果。我们对流动性结果进行了确定性建模,计算了人口健康的平均趋势。我们的模型预测了临床结果的双稳态性:通过确定性计算得出的个体随着时间的推移保持行动能力、行动能力降低或死亡的可能性要么增加到几乎 100%,要么降低到几乎为零。与试图根据概率和相关性来估计最终结果可能性的统计模型相反,我们的模型是根据特定的假设分子机制来预测随着时间推移的功能性结果。我们不是根据随机分布和任意先验来估算概率,而是在实验得出的边界内,在广泛的生理参数值范围内对模型结果进行确定性模拟。我们的研究是 "原理证明",因为它基于一个过于简化的关于通路相互抑制的主要假设。然而,通过这样的假设,可以定性地描述有趣的效应。随着我们对衰老分子机制认识的加深,我们相信这种建模不仅会带来更准确的预测,而且有助于将该领域从主要使用关联研究转向以机理为指导的方法。
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