Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study

被引:58
|
作者
Li, Gloria Hoi-Yee [1 ,2 ]
Cheung, Ching-Lung [1 ]
Chung, Albert Kar-Kin [3 ]
Cheung, Bernard Man-Yung [4 ]
Wong, Ian Chi-Kei [1 ,5 ]
Fok, Marcella Lei Yee [6 ,7 ]
Au, Philip Chun-Ming [1 ]
Sham, Pak-Chung [3 ,8 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Dept Pharmacol & Pharm, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Dept Hlth Technol & Informat, Hong Kong, Peoples R China
[3] Univ Hong Kong, Li Ka Shing Fac Med, Dept Psychiat, Hong Kong, Peoples R China
[4] Univ Hong Kong, Li Ka Shing Fac Med, Dept Med, Hong Kong, Peoples R China
[5] UCL, Sch Pharm, Res Dept Practice & Policy, London, England
[6] Cent & North West London NHS Fdn Trust, London, England
[7] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychol Med, London, England
[8] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Hong Kong, Peoples R China
关键词
Cardiovascular disease; depression; genetics; Mendelian randomization; C-REACTIVE PROTEIN; MYOCARDIAL-INFARCTION; GENETIC-VARIANTS; RISK; METAANALYSIS; MORTALITY; SMOKING; EVENTS; BIAS; AGE;
D O I
10.1017/S0033291720003566
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background Depression and cardiovascular disease (CVD) are associated with each other but their relationship remains unclear. We aim to determine whether genetic predisposition to depression are causally linked to CVD [including coronary artery disease (CAD), myocardial infarction (MI), stroke and atrial fibrillation (AF)]. Methods Using summary statistics from the largest genome-wide association studies (GWAS) or GWAS meta-analysis of depression (primary analysis: n = 500 199), broad depression (help-seeking behavior for problems with nerves, anxiety, tension or depression; secondary analysis: n = 322 580), CAD (n = 184 305), MI (n = 171 875), stroke (n = 446 696) and AF (n = 1 030 836), genetic correlation was tested between two depression phenotypes and CVD [MI, stroke and AF (not CAD as its correlation was previously confirmed)]. Causality was inferred between correlated traits by Mendelian Randomization analyses. Results Both depression phenotypes were genetically correlated with MI (depression: r(G) = 0.169; p = 9.03 x 10(-9); broad depression: r(G) = 0.123; p = 1 x 10(-4)) and AF (depression: r(G) = 0.112; p = 7.80 x 10(-6); broad depression: r(G) = 0.126; p = 3.62 x 10(-6)). Genetically doubling the odds of depression was causally associated with increased risk of CAD (OR = 1.099; 95% CI 1.031-1.170; p = 0.004) and MI (OR = 1.146; 95% CI 1.070-1.228; p = 1.05 x 10(-4)). Adjustment for blood lipid levels/smoking status attenuated the causality between depression and CAD/MI. Null causal association was observed for CVD on depression. A similar pattern of results was observed in the secondary analysis for broad depression. Conclusions Genetic predisposition to depression may have positive causal roles on CAD/MI. Genetic susceptibility to self-awareness of mood problems may be a strong causal risk factor of CAD/MI. Blood lipid levels and smoking may potentially mediate the causal pathway. Prevention and early diagnosis of depression are important in the management of CAD/MI.
引用
收藏
页码:1765 / 1776
页数:12
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