Yang Hua
Department of Gynecology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Pol J Microbiol. 2024 Dec 13;73(4):491-503. doi: 10.33073/pjm-2024-041. eCollection 2024 Dec 1.
Epidemiological studies and animal models have suggested a possible link between gut microbiota (GM), circulating metabolites, and endometriosis (EMs) pathogenesis. However, whether these associations are causal or merely due to confounding factors remains unclear. We conducted a two-sample and two-step Mendelian randomization (MR) study to elucidate the potential causal relationship between GM and EMs, and the mediating role of circulating metabolites. Our MR analysis revealed that higher abundances of class Negativicutes, and order Selenomonadales, as well as genera group, were associated with an increased risk of EMs (Odds Ratio (OR) range: 1.0019-1.0037). Conversely, higher abundances of genera and were linked to reduced risk of EMs (OR range: 0.9964-0.9967). Additionally, elevated levels of circulating metabolites such as 1-eicosatrienoyl-glycerophosphocholine and 1-oleoylglycerophosphocholine were found to be associated with heightened risk of EMs (OR range: 2.21-3.16), while higher concentrations of 3-phenylpropionate and dihomo-linolenate were protective (OR range: 0.285-0.535). Two-step MR analysis indicated that specific microbial taxa, notably genus and order Selenomonadales, might function as mediators linking circulating metabolites to the risk of EMs. Our findings suggest a probable causal relationship between GM, circulating metabolites, and EMs, indicating that GM may mediate the influence of circulating metabolites on the pathophysiology of EMs. These results offer new leads for future mechanistic studies and could inform clinical translational research.
流行病学研究和动物模型表明,肠道微生物群(GM)、循环代谢物与子宫内膜异位症(EMs)发病机制之间可能存在联系。然而,这些关联是因果关系还是仅仅由于混杂因素所致仍不清楚。我们进行了一项两样本两步孟德尔随机化(MR)研究,以阐明GM与EMs之间的潜在因果关系以及循环代谢物的中介作用。我们的MR分析显示,Negativicutes菌纲、Selenomonadales目以及特定属组的丰度较高与EMs风险增加相关(优势比(OR)范围:1.0019 - 1.0037)。相反,特定属的丰度较高与EMs风险降低相关(OR范围:0.9964 - 0.9967)。此外,发现循环代谢物如1 - 二十碳三烯酰 - 甘油磷酸胆碱和1 - 油酰甘油磷酸胆碱水平升高与EMs风险增加相关(OR范围:2.21 - 3.16),而3 - 苯丙酸和二高 - 亚麻酸浓度较高则具有保护作用(OR范围:0.285 - 0.535)。两步MR分析表明,特定的微生物分类群,特别是特定属和Selenomonadales目,可能作为将循环代谢物与EMs风险联系起来的中介。我们的研究结果表明GM、循环代谢物与EMs之间可能存在因果关系,表明GM可能介导循环代谢物对EMs病理生理学的影响。这些结果为未来的机制研究提供了新线索,并可为临床转化研究提供参考。