肠道菌群,循环代谢物和子宫内膜异位症的风险:两步孟德尔随机研究。

Polish journal of microbiology Pub Date : 2024-12-13 eCollection Date: 2024-12-01 DOI:10.33073/pjm-2024-041
Hua Yang
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引用次数: 0

摘要

流行病学研究和动物模型表明,肠道微生物群(GM)、循环代谢物和子宫内膜异位症(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是由于混杂因素造成的尚不清楚。我们进行了一项两样本两步孟德尔随机化(MR)研究,以阐明转基因和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,阴性类、硒单胞菌目、Dialister属、enterorhabduus属、嗜木真杆菌组、Methanobrevibacter属的丰度较高,与EMs的风险增加相关(比值比(OR)范围:1.0019-1.0037)。相反,Coprococcus 1属和Senegalimassilia的丰度越高,EMs的风险就越低(OR范围:0.9964-0.9967)。此外,循环代谢物如1-二十碳三烯酰基甘油酰胆碱和1-油基甘油酰胆碱水平升高被发现与EMs风险增加相关(OR范围:2.21-3.16),而3-苯丙酸盐和二homo-亚麻酸盐浓度较高具有保护作用(OR范围:0.285-0.535)。两步MR分析表明,特定的微生物类群,特别是Enterorhabdus属和Selenomonadales,可能是将循环代谢物与EMs风险联系起来的媒介。我们的研究结果表明转基因、循环代谢物和EMs之间可能存在因果关系,表明转基因可能介导循环代谢物对EMs病理生理的影响。这些结果为未来的机制研究提供了新的线索,并可能为临床转化研究提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut Microbiota, Circulating Metabolites and Risk of Endometriosis: A Two-Step Mendelian Randomization Study.

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 Dialister, Enterorhabdus, Eubacterium xylanophilum group, Methanobrevibacter were associated with an increased risk of EMs (Odds Ratio (OR) range: 1.0019-1.0037). Conversely, higher abundances of genera Coprococcus 1 and Senegalimassilia 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 Enterorhabdus 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.

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