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纵向机器学习将健康衰老因素与慢性疾病风险分离。

Longitudinal machine learning uncouples healthy aging factors from chronic disease risks.

机构信息

Department of Computer Science and Applied Math, Weizmann Institute of Science, Rehovot, Israel.

Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Nat Aging. 2024 Jan;4(1):129-144. doi: 10.1038/s43587-023-00536-5. Epub 2023 Dec 7.

Abstract

To understand human longevity, inherent aging processes must be distinguished from known etiologies leading to age-related chronic diseases. Such deconvolution is difficult to achieve because it requires tracking patients throughout their entire lives. Here, we used machine learning to infer health trajectories over the entire adulthood age range using extrapolation from electronic medical records with partial longitudinal coverage. Using this approach, our model tracked the state of patients who were healthy and free from known chronic disease risk and distinguished individuals with higher or lower longevity potential using a multivariate score. We showed that the model and the markers it uses performed consistently on data from Israeli, British and US populations. For example, mildly low neutrophil counts and alkaline phosphatase levels serve as early indicators of healthy aging that are independent of risk for major chronic diseases. We characterize the heritability and genetic associations of our longevity score and demonstrate at least 1 year of extended lifespan for parents of high-scoring patients compared to matched controls. Longitudinal modeling of healthy individuals is thereby established as a tool for understanding healthy aging and longevity.

摘要

为了了解人类的长寿,必须区分内在的衰老过程和导致与年龄相关的慢性疾病的已知病因。这种去卷积很难实现,因为它需要在患者的整个生命周期内进行跟踪。在这里,我们使用机器学习通过从具有部分纵向覆盖的电子病历中进行外推来推断整个成年期的健康轨迹。使用这种方法,我们的模型可以跟踪健康且没有已知慢性疾病风险的患者的状态,并使用多变量评分来区分具有更高或更低长寿潜力的个体。我们表明,该模型及其使用的标志物在来自以色列、英国和美国人群的数据上表现一致。例如,轻度低中性粒细胞计数和碱性磷酸酶水平是健康衰老的早期指标,与主要慢性疾病的风险无关。我们描述了我们的长寿评分的遗传性和遗传相关性,并证明与匹配的对照组相比,高分患者的父母的寿命至少延长了 1 年。因此,健康个体的纵向建模被确立为理解健康衰老和长寿的工具。

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