AI Article Synopsis

  • The study explores the causal relationship between major depressive disorder (MDD) and venous thromboembolism (VTE) using a Mendelian randomization analysis, referencing genetic data from large biobanks like the Psychiatric Genomics Consortium and UK Biobank.
  • Results show no significant association between MDD and overall VTE risk, but suggestive evidence emerged when adjusting for body mass index and education, with a notable link found between MDD and pulmonary embolism (PE).
  • The findings highlight a potential genetic connection between MDD and VTE risk, while no clear causal links were established between VTE (including PE and deep vein thrombosis) and MDD, indicating the need

Article Abstract

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, = 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, = 0.044). Univariable MR analysis also revealed significant associations between MDD and PE risk (OR: 1.310, 95% CI: 1.073-1.598, = 0.008), but the association between them was no longer significant in MVMR analysis ( = 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11231919PMC
http://dx.doi.org/10.3389/fgene.2024.1383333DOI Listing

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