Evidence map›Paper›PMID 39227644›Full record

ArticleScientific reports2024

Causation between the gut microbiota and inguinal hernia: a two-sample double-sided Mendelian randomization study.

Changyuan Wu, Yujin Zhu, Hongwei Xi

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Changyuan WuDepartment of Pediatrics, Shanxi Medical University, Taiyuan, People's Republic of China.
Yujin ZhuThe First Clinical Medical College, Shanxi Medical University, Taiyuan, People's Republic of China.
Hongwei XiDepartment of General Surgery, Shanxi Children's Hospital, Taiyuan, People's Republic of China. xihongwei148@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inguinal hernias are the most common type of enterocele and are frequently caused by defects in the abdominal wall muscles in the groin area. Numerous animal models and human studies have shown that the gut microbiota is associated with skeletal muscle aging and loss. However, the causation between the gut microbiota and inguinal hernia remains unclear. To reveal the causal association between the gut microbiota and inguinal hernia, we conducted a two-sample double-sided Mendelian randomization analysis. We used genome-wide association analysis (GWAS) summary statistics of the gut microbiota from the MiBioGen consortium and GWAS statistics of inguinal hernia from the FinnGen R10 database. The causation between the gut microbiota and inguinal hernia was explored through the inverse variance weighted (IVW) method, MR Egger regression method, weighted median method, weighted model method, and simple model method. Sensitivity analysis was used to test whether the Mendelian randomization analysis results were reliable. Reverse Mendelian randomization was used to conduct effect analysis and sensitivity analysis using the entire gut microbiota as the outcome. The IVW results indicated that Verrucomicrobia, Lactobacilliales, Clostridiaceae1, Butyricococcus, Categorybacter, Hungatella, Odoribacter, and Olsenella had a direct negative causation with the gut microbiota. The reverse Mendelian Randomization results showed that Eubacterium brachygroup, Eubacterium eligensgroup, Eubacterium xylanophilumgroup, Coprococcus3, Ruminococcus1, and Senegalimassilia were directly related to inguinal hernia. The bilateral sensitivity analysis revealed no heterogeneity or horizontal pleiotropy. The results confirmed that 8 bacterial traits had a negative causation with inguinal hernia. Reverse MR analysis revealed a positive correlation between inguinal hernia and 6 bacterial traits. Modulating the diversity and components of the gut microbiota is envisaged to contribute to improving the incidence and prognosis of inguinal hernia.

Indexed as

Gastrointestinal MicrobiomeGenome-Wide Association StudyHernia, InguinalMendelian Randomization AnalysisHumansPolymorphism, Single NucleotideCausal inferenceGut microbiotaInguinal herniaMendelian randomization

Identifiers

PMID39227644
PMCPMC11372202

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