Causal association between major depressive disorder and venous thromboembolism: a bidirectional mendelian randomization study

被引:2
作者
Li, Hong-Yan [1 ]
Wang, Li-Hong [2 ]
Wang, Jing [1 ]
Wang, Yong-Bo [3 ]
Wang, Hai-Shan [4 ]
机构
[1] Qingdao Univ, Dept Pharm, Med Coll Affiliated, Yantai Yuhuangding Hosp, Yantai, Peoples R China
[2] Qingdao Univ, Dept Ultrasound, Med Coll Affiliated, Yantai Yuhuangding Hosp, Yantai, Peoples R China
[3] Wuhan Univ, Ctr Evidence Based & Translat Med, Zhongnan Hosp, Wuhan, Peoples R China
[4] Yantai Yeda Hosp, Dept Intens Care Unit, Yantai, Peoples R China
关键词
major depressive disorder; venous thromboembolism; risk factor; singlenucleotide polymorphisms; mendelian randomization; BODY-MASS INDEX; THROMBOSIS; RISK; INSTRUMENTS; INFLAMMATION; METAANALYSIS; STRESS;
D O I
10.3389/fgene.2024.1383333
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose Major depressive disorder (MDD) and venous thromboembolism (VTE) may be linked in observational studies. However, the causal association remains ambiguous. Therefore, this study investigates the causal associations between them.Methods We performed a two-sample univariable and multivariable bidirectional Mendelian randomization (MR) analysis to evaluate the associations between MDD and VTE. The summary genetic associations of MDD statistics were obtained from the Psychiatric Genomics Consortium and UK Biobank. Information on VTE, deep vein thrombosis (DVT), and pulmonary embolism (PE) were obtained from the FinnGen Biobank. Inverse-variance weighting was used as the main analysis method. Other methods include weighted median, MR-Egger, Simple mode, and Weighted mode.Results Univariable MR analysis revealed no significant associations between MDD and VTE risk (odds ratio (OR): 0.936, 95% confidence interval (CI): 0.736-1.190, p = 0.590); however, after adjusting the potential relevant polymorphisms of body mass index and education, the multivariable MR analysis showed suggestive evidence of association between them (OR: 1.163, 95% CI: 1.004-1.346, p = 0.044). Univariable MR analysis also revealed significant associations between MDD and PE risk (OR: 1.310, 95% CI: 1.073-1.598, p = 0.008), but the association between them was no longer significant in MVMR analysis (p = 0.072). We found no significant causal effects between MDD and DVT risk in univariable or multivariable MR analyses. There was also no clear evidence showing the causal effects between VTE, PE, or DVT and MDD risk.Conclusion We provide suggestive genetic evidence to support the causal association between MDD and VTE risk. No causal associations were observed between VTE, PE, or DVT and MDD risk. Further validation of these associations and investigations of potential mechanisms are required.
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页数:8
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