Department of Gastroenterology, The First Hospital of Jilin University, Changchun, China.
Front Cell Infect Microbiol. 2024 Jan 4;13:1304858. doi: 10.3389/fcimb.2023.1304858. eCollection 2023.
Significant differences have been discovered between subtypes of Crohn's disease (CD) and ulcerative colitis (UC). The role of gut microbiota in promoting the onset of UC and CD is established, but conclusions regarding subtype-specific analyses remain limited.
This study aims to explore the influence of gut microbiota on subtypes of UC and CD, offering novel insights into the pathogenesis and treatment of UC and CD.Two-sample Mendelian randomization (MR) analysis was employed to examine the causal relationship between subtypes of UC and CD and gut microbiota composition. Gut microbiota data were sourced from the International Consortium MiBioGen, while UC and CD data were obtained from FINNGEN. Eligible single nucleotide polymorphisms (SNPs) were selected as instrumental variables. Multiple analytical approaches such as inverse variance-weighted (IVW), MR-Egger regression, weighted median, weighted mode, and MR-RAPS were utilized. Sensitivity analyses including MR-Egger intercept test, Cochran's Q test, and leave-one-out analysis were conducted for quality control. Subsequently, we employed multivariable IVW, MR-Egger, weighted median, and LASSO regression methods to identify independently significant genera or families and conducted sensitivity analyses.
We have determined that , , and 15 other microbial taxa act as protective factors for various CD and UC subtypes, while , , and 23 other microbial taxa are associated with increased risk for different CD and UC subtypes. Furthermore, through multivariable MR analysis, we have identified significant genera or families with independent effects.
Our study confirms a causal relationship between dysbiosis of gut microbiota and the occurrence of CD and UC subtypes. Furthermore, it validates etiological distinctions among different subtypes of CD and UC. A novel approach to adjunctive therapy involving distinct UC or CD subtypes may involve the use of probiotics and represents a potential avenue for future treatments.
已经发现克罗恩病(CD)和溃疡性结肠炎(UC)的亚型之间存在显著差异。肠道微生物群在促进 UC 和 CD 的发病中的作用已经确立,但关于亚型特异性分析的结论仍然有限。
本研究旨在探讨肠道微生物群对 UC 和 CD 亚型的影响,为 UC 和 CD 的发病机制和治疗提供新的见解。采用两样本孟德尔随机化(MR)分析来研究 UC 和 CD 亚型与肠道微生物群组成之间的因果关系。肠道微生物群数据来自国际微生物组联合组织,而 UC 和 CD 数据来自 FINNGEN。选择合适的单核苷酸多态性(SNP)作为工具变量。采用逆方差加权(IVW)、MR-Egger 回归、加权中位数、加权模式和 MR-RAPS 等多种分析方法。为了质量控制,进行了 MR-Egger 截距检验、Cochran's Q 检验和逐个排除分析的敏感性分析。随后,我们采用多变量 IVW、MR-Egger、加权中位数和 LASSO 回归方法来识别独立显著的属或科,并进行了敏感性分析。
我们确定了 12 种微生物类群和 15 种其他微生物类群作为各种 CD 和 UC 亚型的保护因素,而 22 种微生物类群和 23 种其他微生物类群与不同 CD 和 UC 亚型的风险增加相关。此外,通过多变量 MR 分析,我们确定了具有独立影响的显著属或科。
我们的研究证实了肠道微生物群失调与 CD 和 UC 亚型发生之间存在因果关系。此外,它验证了不同 CD 和 UC 亚型之间的病因学差异。针对不同 UC 或 CD 亚型的辅助治疗的新方法可能涉及使用益生菌,这代表了未来治疗的潜在途径。