Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis

被引:18
作者
Zhuang, Zhenhuang [1 ]
Yao, Minhao [2 ]
Wong, Jason Y. Y. [3 ]
Liu, Zhonghua [2 ]
Huang, Tao [1 ,4 ,5 ]
机构
[1] Peking Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, China 38 Xueyuan Rd, Beijing 100191, Peoples R China
[2] Univ Hong Kong, Dept Stat & Actuarial Sci, Hong Kong, Peoples R China
[3] NCI, Div Canc Epidemiol & Genet, NIH, Rockville, MD USA
[4] Peking Univ, Acad Artificial Intelligence, Ctr Intelligent Publ Hlth, Beijing 100191, Peoples R China
[5] Peking Univ, Minist Educ, Key Lab Mol Cardiovasc Sci, Beijing 100191, Peoples R China
关键词
Body fat percentage; Cardiovascular diseases; Shared genetics; Genetic correlation; Mendelian randomization; MENDELIAN RANDOMIZATION; MASS INDEX; OBESITY; ASSOCIATION; LOCI; METAANALYSIS; EXPRESSION; VARIANTS; RISK; IDENTIFICATION;
D O I
10.1186/s12916-021-01972-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Accumulating evidences have suggested that high body fat percentage (BF%) often occurs in parallel with cardiovascular diseases (CVDs), implying a common etiology between them. However, the shared genetic etiology underlying BF% and CVDs remains unclear. Methods Using large-scale genome-wide association study (GWAS) data, we investigated shared genetics between BF% (N = 100,716) and 10 CVD-related traits (n = 6968-977,323) with linkage disequilibrium score regression, multi-trait analysis of GWAS, and transcriptome-wide association analysis, and evaluated causal associations using Mendelian randomization. Results We found strong positive genetic correlations between BF% and heart failure (HF) (Rg = 0.47, P = 1.27 x 10(- 22)) and coronary artery disease (CAD) (Rg = 0.22, P = 3.26 x 10(- 07)). We identified 5 loci and 32 gene-tissue pairs shared between BF% and HF, as well as 16 loci and 28 gene-tissue pairs shared between BF% and CAD. The loci were enriched in blood vessels and brain tissues, while the gene-tissue pairs were enriched in the nervous, cardiovascular, and exo-/endocrine system. In addition, we observed that BF% was causally related with a higher risk of HF (odds ratio 1.63 per 1-SD increase in BF%, P = 4.16 x 10-04) using a MR approach. Conclusions Our findings suggest that BF% and CVDs have shared genetic etiology and targeted reduction of BF% may improve cardiovascular outcomes. This work advances our understanding of the genetic basis underlying co-morbid obesity and CVDs and opens up a new way for early prevention of CVDs.
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