Department of Pediatrics, Shanxi Medical University, Taiyuan, People's Republic of China.
The First Clinical Medical College, Shanxi Medical University, Taiyuan, People's Republic of China.
Sci Rep. 2024 Sep 4;14(1):20526. doi: 10.1038/s41598-024-71253-1.
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.
腹股沟疝是最常见的疝类型,通常由腹股沟区域腹壁肌肉缺陷引起。大量的动物模型和人类研究表明,肠道微生物群与骨骼肌衰老和丢失有关。然而,肠道微生物群与腹股沟疝之间的因果关系尚不清楚。为了揭示肠道微生物群与腹股沟疝之间的因果关系,我们进行了两样本双侧孟德尔随机化分析。我们使用了 MiBioGen 联盟的肠道微生物群的全基因组关联分析(GWAS)汇总统计数据和 FinnGen R10 数据库的腹股沟疝 GWAS 统计数据。通过逆方差加权(IVW)方法、MR Egger 回归方法、加权中位数方法、加权模型方法和简单模型方法探索了肠道微生物群与腹股沟疝之间的因果关系。敏感性分析用于测试孟德尔随机化分析结果的可靠性。使用整个肠道微生物群作为结果,使用反向孟德尔随机化进行效应分析和敏感性分析。IVW 结果表明,厚壁菌门、乳杆菌目、梭菌科 1 属、丁酸球菌属、分类菌属、Hungatella、Odoribacter 和 Olsenella 与肠道微生物群呈直接负相关。反向孟德尔随机化结果表明,Eubacterium brachygroup、Eubacterium eligensgroup、Eubacterium xylanophilumgroup、Coprococcus3、Ruminococcus1 和 Senegalimassilia 与腹股沟疝直接相关。双侧敏感性分析未发现异质性或水平多效性。结果证实 8 种细菌特征与腹股沟疝呈负相关。反向 MR 分析显示,腹股沟疝与 6 种细菌特征呈正相关。调节肠道微生物群的多样性和组成被认为有助于改善腹股沟疝的发病率和预后。