Xiao Junhao, Tao Zhuoyan, Luo Mingjian, Yan Yong, Ke Shaobiao, Mao Benliang, Zhan Jiulin, Wang Zhe, Wang Bailin, Li Zhiwei
Department of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.
Department of Breast Surgery, Shenzhen Futian Maternal and Child Health Center, Shenzhen, China.
Front Immunol. 2024 Nov 15;15:1452743. doi: 10.3389/fimmu.2024.1452743. eCollection 2024.
Some studies suggest a potential link between intestinal flora and acute pancreatitis (AP). However, the causal relationships between specific intestinal flora and AP, and the possible mediating role of immune cell traits, remain unclear.
A genome-wide association study (GWAS) involving 5,959 participants was conducted to identify genetic instrumental variables associated with 473 intestinal flora taxa. Summary statistics for AP were obtained from the UK Biobank. Immune cell traits were also identified using large-scale GWAS summary data. We employed a two-sample bidirectional Mendelian randomization (MR) approach to investigate the causal relationships between intestinal flora, immune cell traits, and AP, with inverse variance weighting (IVW) as the primary statistical method. Sensitivity analyses, including the MR-Egger intercept test, Cochran's Q test, MR-PRESSO test, and leave-one-out test, were conducted to assess the robustness of our findings. Additionally, we explored whether immune cell traits mediate the pathway from intestinal flora to AP.
11 positive and 11 negative causal relationships were identified between genetic susceptibility in intestinal flora and AP. Furthermore, 19 positive and 9 negative causal relationships were observed between immune cell traits and AP. Notably, CD38 mediated the causal relationship between Bacillus C and AP.
This study is the first to uncover novel causal relationships between various intestinal flora and acute pancreatitis, emphasizing the mediating role of immune cell traits in the pathway from intestinal flora to AP. It also provides new evidence supporting the conditional pathogenicity of the Bacillus genus.
一些研究表明肠道菌群与急性胰腺炎(AP)之间可能存在联系。然而,特定肠道菌群与AP之间的因果关系以及免疫细胞特征可能的中介作用仍不清楚。
进行了一项涉及5959名参与者的全基因组关联研究(GWAS),以确定与473种肠道菌群分类群相关的遗传工具变量。AP的汇总统计数据来自英国生物银行。还使用大规模GWAS汇总数据确定了免疫细胞特征。我们采用两样本双向孟德尔随机化(MR)方法来研究肠道菌群、免疫细胞特征和AP之间的因果关系,以逆方差加权(IVW)作为主要统计方法。进行了敏感性分析,包括MR-Egger截距检验、 Cochr an's Q检验、MR-PRESSO检验和留一法检验,以评估我们研究结果的稳健性。此外,我们探讨了免疫细胞特征是否介导了从肠道菌群到AP的途径。
在肠道菌群的遗传易感性与AP之间确定了11个正向和11个负向因果关系。此外,在免疫细胞特征与AP之间观察到19个正向和9个负向因果关系。值得注意的是,CD38介导了芽孢杆菌C与AP之间的因果关系。
本研究首次揭示了各种肠道菌群与急性胰腺炎之间的新因果关系,强调了免疫细胞特征在从肠道菌群到AP的途径中的中介作用。它还提供了新的证据支持芽孢杆菌属的条件致病性。