The bidirectional association between frailty index and cardiovascular disease: A Mendelian randomization study

被引:3
|
作者
Xu, Qingyun [1 ,2 ]
Jia, Yiming [1 ,2 ]
Wang, Yinan [1 ,2 ]
Yang, Pinni [1 ,2 ]
Sun, Lulu [1 ,2 ]
Liu, Yi [1 ,2 ]
Chang, Xinyue [1 ,2 ]
He, Yu [1 ,2 ]
Guo, Daoxia [3 ]
Shi, Mengyao [1 ,2 ]
Zhang, Yonghong [1 ,2 ]
Zhu, Zhengbao [1 ,2 ]
机构
[1] Soochow Univ, Sch Publ Hlth, Dept Epidemiol, Suzhou Med Coll, 199 Renai Rd,Ind Pk Dist, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Prevent & Translat Med Geriatr Dis, Suzhou Med Coll, 199 Renai Rd,Ind Pk Dist, Suzhou 215123, Jiangsu, Peoples R China
[3] Soochow Univ, Med Coll, Sch Nursing, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Frailty; Hypertension; Myocardial infarction; Heart failure; Atrial fibrillation; Mendelian randomization; GENOME-WIDE ASSOCIATION; OXIDATIVE STRESS; OLDER-ADULTS; RISK; INFLAMMATION; METAANALYSIS; INSTRUMENTS; HEALTH;
D O I
10.1016/j.numecd.2023.10.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aim: Observational studies have suggested a relationship between frailty and cardiovascular disease (CVD), but the causality is still uncertain. We used bidirectional Mendelian randomization (MR) design to investigate the potential causal associations between frailty and four main CVDs, including hypertension, myocardial infarction (MI), heart failure (HF), and atrial fibrillation (AF). Methods and results: Independent single-nucleotide polymorphisms for frailty index (FI) and CVDs (hypertension, MI, HF, and AF) were selected as genetic instruments based on Europeandescent genome-wide association studies (GWASs). Summary-level data for outcomes on FI (n = 175,226), hypertension (n = 463,010), MI (n = 171,875), HF (n = 977323), and AF (n = 1,030,836) was derived from five large-scale GWASs of European ancestry. We used the inverse-variance weighted (IVW) method to examine the bidirectional associations between FI and CVDs in the main analyses. In the IVW MR analyses, genetically determined high FI was significantly associated with increased risks of hypertension (odds ratio [OR] per 1-SD increase: 1.07 [95 % confidence interval, 1.05-1.08]), MI (OR per 1-SD increase: 1.74 [1.21-2.51]), HF (OR per 1-SD increase: 1.28 [1.10-1.48]), and AF (OR per 1-SD increase: 1.20 [1.08-1.33]). In addition, genetically determined hypertension (beta: 1.406 [1.225-1.587]), MI (beta: 0.045 [0.023 -0.067]), HF (beta: 0.105 [0.066-0.143]) and AF (beta: 0.021 [0.012-0.031]) were significantly associated with high FI. These findings were robustly supported by a series of sensitivity analyses with different MR models. Conclusions: We found potential bidirectional causal associations between elevated FI and increased risks of CVD, suggesting mutual risk factors between frailty and CVD. (c) 2023 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:624 / 632
页数:9
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