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Murine Fecal Isolation and Microbiota Transplantation
Published on: May 26, 2023
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The causality between gut microbiota and functional dyspepsia: A two-sample Mendelian randomization analysis.
Xiaojing Jin1, Keli Xu1, Jingyi Wu1
1The Third Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.
Medicine
|October 29, 2024
Summary
This study used Mendelian randomization to link gut microbiota and functional dyspepsia (FD). Certain gut bacteria were found to be associated with an increased or decreased risk of developing FD.
Area of Science:
- Gastroenterology
- Microbiome Research
- Genetics
Background:
- Functional dyspepsia (FD) is a common gastrointestinal disorder with complex etiology.
- The role of gut microbiota in FD pathogenesis is increasingly recognized but not fully elucidated.
Purpose of the Study:
- To investigate the causal relationship between gut microbiota and functional dyspepsia (FD) using a two-sample Mendelian randomization (MR) approach.
- To identify specific gut microbial taxa associated with FD risk.
Main Methods:
- Utilized genome-wide association studies (GWAS) data for gut microbiota (n=18,340) and FD (n=189,695 controls, 4376 cases).
- Employed inverse variance weighted (IVW) analysis as the primary method for MR analysis.
- Conducted sensitivity analyses to assess pleiotropy and heterogeneity, ensuring result reliability.
Main Results:
- Identified seven gut microbial taxa significantly associated with FD.
- Positive associations with FD were observed for Order/Family Erysipelotrichales, Genus Haemophilus, Genus Ruminiclostridium 9, and Genus Lachnospiraceae NK4A 136 group.
- Inverse associations with FD were found for Class Gammaproteobacteria and Genus Erysipelatoclostridium.
Conclusions:
- This MR study provides genetic evidence supporting a link between specific gut microbiota and functional dyspepsia.
- Findings suggest that alterations in gut microbial composition may contribute to FD development.
- Further research is warranted to explore the mechanisms underlying the gut microbiota-FD relationship.

