Marital and living status and biological ageing trajectories: a longitudinal cohort study with a 20-year follow-up.

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Weiyao Yin, Xia Li, Ruoqing Chen, Yiqiang Zhan, Juulia Jylhävä, Fang Fang, Sara Hägg
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Abstract

Biomarkers of ageing (BA) can predict health risks beyond chronological age, but little is known about how marital/living status affects longitudinal changes in BA. We examined the association between marital/living status and BA over time using the-Swedish-Adoption/Twin-Study-of-Aging (SATSA) cohort. Four BAs were analyzed: telomere length (TL) (638 individuals; 1603 measurements), DNAmAge (535 individuals; 1392 measurements), cognition (823 individuals; 3218 measurements), and frailty index (FI) (1828 individuals; 9502 measurements). Individuals were born between 1900 and 1948, and data on marital/living status, BAs, and covariates were collected through nine waves of questionnaires and in-person testing from 1986 to 2014. Mixed linear regression with random effects at twin-pair and individual levels were used to assess BA changes for constant marital/living status. Conditional generalized estimating equation assessed within-individual BA changes for varying marital/living status. Results showed that individuals who were consistently unmarried/non-cohabiting (β = 0.291, 95%CI = 0.189-0.393) or living alone (β = 0.203, 95%CI = 0.090-0.316) were more frail, and experienced accelerated frailty (p-for-interaction with age < 0.001 for marital status; p-for-interaction = 0.002 for living status) and cognitive decline (p-for-interaction < 0.001), compared to those married/cohabiting or living with someone Among individuals whose marital/living status changed, frailty was higher when living alone (β = 0.089, 95%CI = 0.017-0.162) and frailty accelerated when they became unmarried/non-cohabiting or were living alone (p-for-interaction < 0.001). Cognitive decline also accelerated when living alone (p-for-interaction = 0.020). No associations were observed for TL and DNAmAge. In conclusion, being unmarried/non-cohabiting or living alone from mid-to-old age is linked to accelerated cognitive decline and frailty. These findings highlight the potential importance of social support networks and living arrangements for healthy ageing.

婚姻和生活状况与生物衰老轨迹:一项20年随访的纵向队列研究。
衰老生物标志物(BA)可以预测超出实足年龄的健康风险,但对婚姻/生活状况如何影响BA的纵向变化知之甚少。我们使用瑞典收养/老龄化双胞胎研究(SATSA)队列研究了婚姻/生活状况与BA之间的关系。分析了4种BAs:端粒长度(TL)(638例);1603测量),DNAmAge(535个人;1392个测量值),认知(823个个体;虚弱指数(FI)(1828个个体;9502测量)。研究对象出生于1900年至1948年之间,从1986年至2014年,通过九波问卷调查和现场测试收集了婚姻/生活状况、BAs和协变量的数据。采用混合线性回归与随机效应在双胞胎和个体水平评估BA变化恒定的婚姻/生活状态。条件广义估计方程评估了不同婚姻/生活状态下个体内BA的变化。结果显示,长期未婚/非同居(β = 0.291, 95%CI = 0.189-0.393)或独居(β = 0.203, 95%CI = 0.090-0.316)的个体更虚弱,并且随着年龄的增加而加速虚弱
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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