Major depressive disorder and cardiometabolic diseases: a bidirectional Mendelian randomisation study

被引:61
|
作者
Tang, Bowen [1 ]
Yuan, Shuai [1 ,2 ,3 ]
Xiong, Ying [1 ]
He, Qiqiang [4 ]
Larsson, Susanna C. [2 ,3 ]
机构
[1] Karolinska Inst, Dept Global Publ Hlth, Stockholm, Sweden
[2] Karolinska Inst, Inst Environm Med, Unit Cardiovasc & Nutr Epidemiol, Stockholm, Sweden
[3] Uppsala Univ, Dept Surg Sci, Dag Hammarskjold Vag 14B, S-75185 Uppsala, Sweden
[4] Wuhan Univ, Sch Hlth Sci, Dept Nutr & Food Hyg, Wuhan, Peoples R China
基金
瑞典研究理事会;
关键词
Coronary artery disease; Heart failure; Major depression disorder; Mendelian randomisation analysis; Type; 2; diabetes; TYPE-2; DIABETES-MELLITUS; HEART-FAILURE; RISK-FACTOR; ASSOCIATION; US; EPIDEMIOLOGY; PREVALENCE; SYMPTOMS; ADULTS;
D O I
10.1007/s00125-020-05131-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis Observational studies have shown a bidirectional association between major depressive disorder (MDD) and cardiometabolic diseases. We conducted a two-sample bidirectional Mendelian randomisation (MR) study to assess the causal associations of MDD with type 2 diabetes, coronary artery disease (CAD) and heart failure and vice versa. Methods We extracted summary-level data for MDD, type 2 diabetes, CAD and heart failure from corresponding published large genome-wide association studies of individuals mainly of European-descent. In total, 96 SNPs for MDD, 202 SNPs for type 2 diabetes, 44 SNPs for CAD and 12 SNPs for heart failure were proposed as instrumental variables at the genome-wide significance level (p < 5 x 10(-8)). The random-effects inverse-variance weighted method was used for the main analyses. Results Genetic liability to MDD was significantly associated with type 2 diabetes and CAD at the Bonferroni-corrected significance level. The ORs of type 2 diabetes and CAD were respectively 1.26 (95% CI 1.10, 1.43; p = 6 x 10(-4)) and 1.16 (95% CI 1.05, 1.29; p = 0.0047) per one-unit increase in log(e) odds of MDD. There was a suggestive association between MDD and heart failure (OR 1.11 [95% CI 1.01, 1.21]; p = 0.033). We found limited evidence supporting causal effects of cardiometabolic diseases on MDD risk in the reverse MR analyses. Conclusions/interpretation The present study strengthened the evidence that MDD is a potential risk factor for type 2 diabetes and CAD. Whether MDD is causally related to heart failure needs further study. Data availability All data included in this study were uploaded as supplements and are also publicly available through published GWASs and open GWAS datasets (UK Biobank, 23andMe and Psychiatric Genomics: https://datashare.is.ed.ac.uk/handle/10283/3203; DIAGRAM: http://diagram-consortium.org/downloads.html; CARDIoGRAMplusCD4: www.cardiogramplusc4d.org/; HERMES: http://www.kp4cd.org/datasets/mi).
引用
收藏
页码:1305 / 1311
页数:7
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