主观健康测量基因结构的年龄和性别差异:与身体健康、抑郁症状和外显记忆的关系

Deborah Finkel, Margaret Gatz, Carol E Franz, Vibeke S Catts, Kaare Christensen, William Kremen, Marianne Nygaard, Brenda L Plassman, Perminder S Sachdev, Keith Whitfield, Nancy L Pedersen
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引用次数: 0

摘要

目标 主观健康(SH)不仅是身体健康的指标,还反映了对自身健康信息的积极认知处理,并与神经质和抑郁等情绪健康指标相关联。行为遗传学方法研究了SH的遗传结构,即遗传和环境对SH个体差异的影响,以及与身体、认知和情绪健康等潜在成分的关联。以往的双生子分析受到性别、样本大小、年龄范围以及对单一协变量的关注等因素的限制。方法 目前的分析使用了来自国际基因与环境相互作用多重研究(IGEMS)联盟的 24173 名年龄在 40-90 岁之间的成年人的数据,研究了 SH 的三个测量指标的遗传结构:自评健康、与他人相比的健康以及健康对活动的影响。SH的独立路径模型包括身体健康、抑郁症状和外显记忆,年龄、性别和国家为协变量。结果 SH 指标的大部分或全部遗传变异与身体健康、抑郁症状和外显记忆共享。不同测量指标、不同年龄组(40-65 岁、66-90 岁)和不同性别的 SH 遗传结构各不相同。年龄比较显示,老年人与所有 3 个协变量的相关性更强,这通常是由于共享的遗传变异更大所致。讨论 SH 的预测价值已得到充分证明。随着年龄的增长,SH 越来越被认为是一个人生命储备的直观总和。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age and sex differences in the genetic architecture of measures of subjective health: Relationships with physical health, depressive symptoms, and episodic memory
Objectives Subjective health (SH) is not just an indicator of physical health, but also reflects active cognitive processing of information about one’s own health and has been associated with emotional health measures, such as neuroticism and depression. Behavior genetic approaches investigate the genetic architecture of SH, i.e., genetic and environmental influences on individual differences in SH and associations with potential components such as physical, cognitive, and emotional health. Previous twin analyses have been limited by sex, sample size, age range, and focus on single covariates. Methods The current analysis used data from 24,173 adults ranging in age from 40-90 years from the international Interplay of Genes and Environment Across Multiple Studies (IGEMS) consortium to investigate the genetic architecture of three measures of SH: self-rated health, health compared to others, and impact of health on activities. Independent pathways model of SH included physical health, depressive symptoms, and episodic memory, with age, sex, and country included as covariates. Results Most or all of the genetic variance for SH measures was shared with physical health, depressive symptoms, and episodic memory. Genetic architecture of SH differed across measures, age groups (40-65, 66-90), and sexes. Age comparisons indicated stronger correlations with all 3 covariates in older adults, often resulting from greater shared genetic variance. Discussion The predictive value of SH has been amply demonstrated. The higher genetic contributions to associations between SH and its components in older adults support the increasing conceptualization with age of SH as an intuitive summation of one’s vital reserve.
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