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遗传易感性、可改变的生活方式及其对人类寿命的综合影响:来自多项队列研究的证据。

Genetic predisposition, modifiable lifestyles, and their joint effects on human lifespan: evidence from multiple cohort studies.

机构信息

Department of Big Data in Health Science, School of Public Health and Center of Clinical Big Data and Analytics of The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Department of Biostatistics, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.

出版信息

BMJ Evid Based Med. 2024 Jul 23;29(4):255-263. doi: 10.1136/bmjebm-2023-112583.

Abstract

OBJECTIVE

To investigate the associations across genetic and lifestyle factors with lifespan.

DESIGN

A longitudinal cohort study.

SETTING

UK Biobank.

PARTICIPANTS

353 742 adults of European ancestry, who were recruited from 2006 to 2010 and were followed up until 2021.

EXPOSURES

A polygenic risk score for lifespan with long (<lowest quintile), intermediate (quintiles 2 to 4), and short (>highest quintile) risk categories and a weighted healthy lifestyle score, including no current smoking, moderate alcohol consumption, regular physical activity, healthy body shape, adequate sleep duration, and a healthy diet, categorised into favourable, intermediate, and unfavourable lifestyles.

MAIN OUTCOME MEASURES

Lifespan defined as the date of death or the censor date minus the date of birth.

RESULTS

Of the included 353 742 participants of European ancestry with a median follow-up of 12.86 years, 24 239 death cases were identified. Participants were grouped into three genetically determined lifespan categories including long (20.1%), intermediate (60.1%), and short (19.8%), and into three lifestyle score categories including favourable (23.1%), intermediate (55.6%), and unfavourable (21.3%). The hazard ratio (HR) of death for individuals with a genetic predisposition to a short lifespan was 1.21 (95% CI 1.16 to 1.26) compared to those with a genetic predisposition to a long lifespan. The HR of death for individuals in the unfavourable lifestyle category was 1.78 (95% CI 1.71 to 1.85), compared with those in the favourable lifestyle category. Participants with a genetic predisposition to a short lifespan and an unfavourable lifestyle had 2.04 times (95% CI 1.87 to 2.22) higher rates of death compared with those with a genetic predisposition to a long lifespan and a favourable lifestyle. No multiplicative interaction was detected between the polygenic risk score of lifespan and the weighted healthy lifestyle score (p=0.10). The optimal combination of healthy lifestyles, including never smoking, regular physical activity, adequate sleep duration, and a healthy diet, was derived to decrease risk of premature death (death before 75 years).

CONCLUSION

Genetic and lifestyle factors were independently associated with lifespan. Adherence to healthy lifestyles could largely attenuate the genetic risk of a shorter lifespan or premature death. The optimal combination of healthy lifestyles could convey better benefits for a longer lifespan, regardless of genetic background.

摘要

目的

探讨遗传和生活方式因素与寿命之间的关联。

设计

纵向队列研究。

地点

英国生物银行。

参与者

353742 名欧洲血统的成年人,他们于 2006 年至 2010 年招募,并随访至 2021 年。

暴露因素

寿命的多基因风险评分,分为长(<最低五分位数)、中(五分位数 2 到 4)和短(>最高五分位数)风险类别,以及加权健康生活方式评分,包括不吸烟、适度饮酒、定期体育锻炼、健康体型、充足的睡眠时间和健康饮食,分为有利、中等和不利生活方式。

主要观察指标

寿命定义为死亡日期或删失日期减去出生日期。

结果

在纳入的 353742 名具有欧洲血统的参与者中,中位随访时间为 12.86 年,共确定了 24239 例死亡病例。参与者被分为三组,根据遗传决定的寿命分为长(20.1%)、中(60.1%)和短(19.8%),以及三组生活方式评分分为有利(23.1%)、中等(55.6%)和不利(21.3%)。与遗传倾向寿命较长的个体相比,遗传倾向寿命较短的个体死亡的风险比(HR)为 1.21(95%CI 1.16 至 1.26)。不利生活方式类别的个体死亡的 HR 为 1.78(95%CI 1.71 至 1.85),而有利生活方式类别的个体死亡的 HR 为 1.78(95%CI 1.71 至 1.85)。与遗传倾向寿命较长且生活方式有利的个体相比,遗传倾向寿命较短且生活方式不利的个体死亡的风险高 2.04 倍(95%CI 1.87 至 2.22)。未检测到寿命多基因风险评分与加权健康生活方式评分之间存在乘法交互作用(p=0.10)。得出了健康生活方式的最佳组合,包括从不吸烟、定期进行体育锻炼、保持充足的睡眠时间和健康饮食,可以降低早逝(75 岁前死亡)的风险。

结论

遗传和生活方式因素与寿命独立相关。坚持健康的生活方式可以在很大程度上减轻寿命较短或早逝的遗传风险。健康生活方式的最佳组合可以带来更长的寿命,而与遗传背景无关。

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