确定影响表型年龄和计时年龄之间差距的生物标记和社会人口因素。

Daniele Pala, Jia Xu, Yuezhi Xie, Yuqin Zhang, Li Shen
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引用次数: 0

摘要

导言:世界人口正在迅速老龄化,与年龄相关的心血管和神经退行性疾病增加了公共卫生和经济负担。早期风险检测对于预防和提高老年人的生活质量至关重要。此外,与衰老相关的健康风险并不直接与年龄相关,还受到环境暴露的综合影响。过去的研究提出了 "表型年龄 "的概念,即结合年龄和生物标志物来估计个人的健康风险:本研究探讨了哪些因素是造成计时年龄与表型年龄之间差距的主要原因。我们将十种机器学习回归技术结合应用于 NHANES 数据集,其中包含 41,474 名患者的人口学、实验室和社会经济数据,以确定最重要的特征。然后,我们使用聚类分析和混合效应模型按性别、种族和教育程度进行分层:结果:我们确定了 28 个与表型年龄和实际年龄之间存在显著差距有关的人口、生物和环境因素。根据性别、教育程度和种族进行分层后,我们发现结果分布存在显著的统计学差异:通过证明健康风险预防应同时考虑生物和社会人口因素,我们提供了一种预测老龄化率的新方法,并有可能改进针对老年相关疾病的预防策略。
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Identifying biological markers and sociodemographic factors that influence the gap between phenotypic and chronological ages.

Introduction: The world's population is aging rapidly, leading to increased public health and economic burdens due to age-related cardiovascular and neurodegenerative diseases. Early risk detection is essential for prevention and to improve the quality of life in elderly individuals. Plus, health risks associated with aging are not directly tied to chronological age, but are also influenced by a combination of environmental exposures. Past research has introduced the concept of "Phenotypic Age," which combines age with biomarkers to estimate an individual's health risk.

Methods: This study explores which factors contribute most to the gap between chronological and phenotypic ages. We combined ten machine learning regression techniques applied to the NHANES dataset, containing demographic, laboratory and socioeconomic data from 41,474 patients, to identify the most important features. We then used clustering analysis and a mixed-effects model to stratify by sex, ethnicity, and education.

Results: We identified 28 demographic, biological and environmental factors related to a significant gap between phenotypic and chronological ages. Stratifying for sex, education and ethnicity, we found statistically significant differences in the outcome distributions.

Conclusion: By showing that health risk prevention should consider both biological and sociodemographic factors, we offer a new approach to predict aging rates and potentially improve targeted prevention strategies for age-related conditions.

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