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Causal linkage of tobacco smoking with ageing: Mendelian randomization analysis towards telomere attrition and sarcopenia

孟德尔随机化 肌萎缩 多效性 观察研究 医学 老化 全基因组关联研究 人口学 体质指数 临床营养学 老年学 内科学 遗传学 单核苷酸多态性 生物 表型 遗传变异 基因型 社会学 基因
作者
Sehoon Park,Seong Geun Kim,Soojin Lee,Yaerim Kim,Semin Cho,Kwangsoo Kim,Yong Chul Kim,Seung Seok Han,Hajeong Lee,Jung Pyo Lee,Kwon Wook Joo,Chun Soo Lim,Yon Su Kim,Dong Ki Kim
出处
期刊:Journal of Cachexia, Sarcopenia and Muscle [Springer Science+Business Media]
卷期号:14 (2): 955-963 被引量:22
标识
DOI:10.1002/jcsm.13174
摘要

Abstract Background Ageing traits and frailty are important health issues in modern medicine. Evidence supporting the causal effects of tobacco smoking on various ageing traits is required. Methods This study performed Mendelian randomization (MR) analysis instrumenting 377 genetic variants associated with being an ever‐smoker at a genome‐wide significance level to test the causal estimates from tobacco smoking. The outcome data were obtained from 337 138 white British ancestry participants from the UK Biobank. Leucocyte telomere length, appendicular lean mass index, subjective walking pace, handgrip strength, and wristband accelerometry‐determined physical activity degree were collected as ageing‐related outcomes. Summary‐level MR analysis was performed using the inverse variance‐weighted method and pleiotropy‐robust MR methods, including weighted median and MR‐Egger. Observational association between the outcome traits and phenotypically being an ever‐smoker was also investigated. Results Summary‐level MR analysis indicated that a higher genetic predisposition for tobacco smoking was significantly associated with shorter leucocyte telomere length (twofold increase in prevalence of smoking towards standardized Z‐score, −0.041 [−0.054, −0.028]), lower appendicular lean mass index (−0.007 [−0.010, −0.005]), slower walking pace (ordinal category, −0.047 [−0.054, −0.033]) and lower time spent on moderate‐to‐vigorous physical activity (hours per week, −0.39 [−0.56, −0.23]). The causal estimates were non‐significant towards handgrip strength phenotype (kg, 0.074 [−0.055, 0.204]). Pleiotropy‐robust MR results generally supported the main causal estimates. The observational findings also showed significant association between being an ever‐smoker and the ageing traits. Conclusions Genetically predicted and observational tobacco smoking status are significantly associated with poor ageing phenotypes. Healthcare providers may continue to reduce tobacco use, which may be helpful in reducing the burden of ageing and frailty.

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