The association between the basal metabolic rate and cardiovascular disease: A two‐sample Mendelian randomization study

孟德尔随机化 内科学 医学 置信区间 优势比 多效性 心脏病学 基础代谢率 冠状动脉疾病 心房颤动 全基因组关联研究 单核苷酸多态性 生物 遗传学 遗传变异 基因型 表型 基因
作者
K. Chen,Yue Zhang,Siyu Zhou,Chengjiang Jin,Meixiang Xiang,Hong Ma
出处
期刊:European Journal of Clinical Investigation [Wiley]
卷期号:54 (5) 被引量:4
标识
DOI:10.1111/eci.14153
摘要

Abstract Background Mendelian randomization analysis was applied to elucidate the causal relationship between the basal metabolic rate (BMR) and common cardiovascular diseases. Method We choose BMR as exposure. BMR is the metabolic rate of the body when the basic physiological activities (blood circulation, breathing and constant body temperature) are maintained. The normal BMR is 1507 kcal/day for men and 1276 kcal/day for women. The dataset was drawn from the public GWAS dataset (GWAS ID: ukb‐a‐268), collected and analysed by UK biobank, containing 331,307 European males and females. SNPs independently and strongly associated with BMR were used as instrumental variables in the inverse variance weighted analysis. MR‐Egger, weighted median, MR pleiotropy residual sum, and outlier methods were also performed, and the sensitivity was evaluated using horizontal pleiotropy and heterogeneity analyses to ensure the stability of the results. Results An increased BMR is associated with a higher risk of cardiomyopathy (odds ratio [OR] = 2.00, 95% confidence interval [CI], 1.57–2.54, p = 1.87 × 10 −8 ), heart failure (OR = 1.39, 95% CI, 1.27–2.51, p = 8.1 × 10 −13 ), and valvular heart disease (OR = 1.18, 95% CI, 1.10–1.27, p = .00001). However, there was no clear association between BMR and the subtypes of other cardiovascular diseases, such as coronary disease (OR = .96, 95% CI, .85–1.08, p = .48651) and atrial fibrillation (AF) (OR = 1.85, 95% CI, 1.70–2.02, p = 6.28 × 10 −44 ). Conclusion Our study reveals a possible causal effect of BMR on the risk of cardiomyopathy, heart failure and valvular disease, but not for coronary disease and AF.
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