Systematic Mendelian randomization study of the effect of gut microbiome and plasma metabolome on venous thromboembolism

Author:

Cheng Pengfei1,He Yuan1,hu junjie2,Ye Da-Wei2,Wang Wei-Ci2,Wang Jin-Xi1

Affiliation:

1. Third Hospital of Shanxi Medical University, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital

2. Huazhong University of Science and Technology

Abstract

Abstract Background Although there is considerable evidence suggesting a link between gut microbiota (GM) composition and venous thromboembolism (VTE)/deep vein thrombosis (DVT)/pulmonary embolism (PE), population-level studies that can establish a causal relationship are currently lacking. Methods Using two-sample Mendelian randomization (MR) approach was used to examine the causal effects of 211 GM and 489 plasma metabolites on VTE/PE/DVT. We employed instrumental variables comprised of single nucleotide polymorphisms (SNPs) strongly associated with GM composition and plasma metabolite levels to determine whether these factors play a causal role in the development of VTE/DVT/PE. Additionally, we conducted mediation analysis to explore the potential associations between specific taxonomic groups and metabolites. Results The MR analysis revealed significant associations between 16 taxonomic units and 40 metabolites with VTE/DVT/PE as the causative factors. Among these, Firmicutes, Clostridia, Roseburia, Ruminococcaceae NK4A214, and Intestinimonas were found to have a protective effect against VTE/DVT/PE. In contrast, Bacteroidetes, Anaerotruncus, Victivallales, Desulfovibrionaceae, Clostridium innocuum, Eubacterium oxidoreducens, and Lachnoclostridium have been identified as risk factors for VTE/DVT/PE. Reverse MR analysis revealed 11 associations between VTE/DVT/PE and GM. Furthermore, no significant heterogeneity or horizontal pleiotropy was observed in any of the instrumental variables. Mediation analysis revealed 10 intermediate relationships, and metabolic pathway analysis identified 6 significant pathways. Conclusions Our study emphasizes the significant causal associations between the gut microbiota (GM), plasma metabolome, and VTE/DVT/PE. These interconnections have the potential to be used as clinical biomarkers for risk stratification and prognosis assessment in patients with VTE/DVT/PE.

Publisher

Research Square Platform LLC

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