孟德尔随机化
肌萎缩
认知
学历
老年学
医学
因果关系(物理学)
心理学
内科学
遗传学
生物
精神科
遗传变异
物理
量子力学
基因
基因型
经济
经济增长
作者
Yanyan Li,Zhenhuang Zhuang,Huaxin Si,Qinqin Liu,Jiaqi Yu,Wendie Zhou,Tao Huang,Cuili Wang
标识
DOI:10.1177/10998004241274271
摘要
Purpose Two-sample Mendelian randomization methods were used to explore the causal effects of cognitive reserve proxies, such as educational attainment, occupational attainment, and physical activity (PA), on biological (leukocyte telomere length), phenotypic (sarcopenia-related features), and functional (frailty index and cognitive performance) aging levels. Results Educational attainment had a potential protective effect on the telomere length ( β = 0.10, 95% CI: 0.08–0.11), sarcopenia-related features ( β = 0.04–0.24, 95% CI: 0.02–0.27), frailty risk ( β = −0.31, 95% CI: −0.33 to −0.28), cognitive performance ( β = 0.77, 95% CI: 0.75–0.80). Occupational attainment was causally related with sarcopenia-related features ( β = 0.07–0.10, 95% CI: 0.05–0.14), and cognitive performance ( β = 0.30, 95% CI: 0.24–0.36). Device-measured PA was potentially associated with one sarcopenia-related feature ( β = 0.14, 95% CI: 0.03–0.25). Conclusions Our findings support the potential causality of educational attainment on biological, phenotypic, and functional aging outcomes, of occupational attainment on phenotypic and functional aging-related outcomes, and of PA on phenotypic aging-related outcomes.
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