Gut Microbiome and Stroke: a Bidirectional Mendelian Randomisation Study in East Asian and European Populations.

IF 2.6 1区 医学 Journal of Investigative Medicine Pub Date : 2024-01-31 DOI:10.1136/svn-2023-002717
Shiyao Cheng, Hao Zheng, Yuandan Wei, Xingchen Lin, Yuqin Gu, Xinxin Guo, Zhe Fan, Hao Li, Si Cheng, Siyang Liu
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Abstract

Background and aims: Observational studies have implicated the involvement of gut microbiome in stroke development. Conversely, stroke may disrupt the gut microbiome balance, potentially causing systemic infections exacerbated brain infarction. However, the causal relationship remains controversial or unknown. To investigate bidirectional causality and potential ethnic differences, we conducted a bidirectional two-sample Mendelian randomisation (MR) study in both East Asian (EAS) and European (EU) populations.

Methods: Leveraging the hitherto largest genome-wide association study (GWAS) summary data from the MiBioGen Consortium (n=18 340, EU) and BGI (n=2524, EAS) for the gut microbiome, stroke GWAS data from the GIGASTROKE Consortium(264 655 EAS and 1 308 460 EU), we conducted bidirectional MR and sensitivity analyses separately for the EAS and EU population.

Results: We identified nominally significant associations between 85 gut microbiomes taxa in EAS and 64 gut microbiomes taxa in EU with stroke or its subtypes. Following multiple testing, we observed that genetically determined 1 SD increase in the relative abundance of species Bacteroides pectinophilus decreased the risk of cardioembolic stroke onset by 28% (OR 0.72 (95% CI 0.62 to 0.84); p=4.22e-5), and that genetically determined 1 SD increase in class Negativicutes resulted in a 0.76% risk increase in small vessel stroke in EAS. No significant causal association was identified in the EU population and the reverse MR analysis.

Conclusion: Our study revealed subtype-specific and population-specific causal associations between gut microbiome and stroke risk among EAS and EU populations. The identified causality holds promise for developing a new stroke prevention strategy, warrants further mechanistic validation and necessitates clinical trial studies.

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肠道微生物组与中风:东亚和欧洲人群的双向孟德尔随机研究。
背景和目的:观察性研究表明,肠道微生物组参与了中风的发病过程。反之,中风可能会破坏肠道微生物组的平衡,从而可能导致全身感染,加重脑梗塞。然而,其因果关系仍存在争议或未知。为了研究双向因果关系和潜在的种族差异,我们在东亚(EAS)和欧洲(EU)人群中开展了一项双向双样本孟德尔随机化(MR)研究:利用迄今为止最大的全基因组关联研究(GWAS)汇总数据,包括肠道微生物组的 MiBioGen 联合会(18 340 人,欧盟)和 BGI(2524 人,东亚),以及中风 GWAS 数据,包括 GIGASTROKE 联合会(264 655 人,东亚和欧盟),我们分别对东亚和欧盟人群进行了双向 MR 和敏感性分析:我们在 EAS 和欧盟人群中分别发现了 85 个肠道微生物群分类群和 64 个肠道微生物群分类群与中风或中风亚型之间存在明显的关联。经过多重检验,我们发现,果胶嗜酸乳杆菌(Bacteroides pectinophilus)物种相对丰度的基因决定性1 SD增加可使心血管栓塞性中风发病风险降低28%(OR 0.72 (95% CI 0.62 to 0.84); p=4.22e-5),而阴性类群(Negativicutes)的基因决定性1 SD增加可导致EAS人群小血管中风风险增加0.76%。在欧盟人群和反向 MR 分析中未发现明显的因果关系:我们的研究揭示了肠道微生物组与 EAS 和欧盟人群中风风险之间的亚型特异性和人群特异性因果关系。已确定的因果关系为制定新的中风预防策略带来了希望,需要进一步的机理验证和临床试验研究。
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来源期刊
Journal of Investigative Medicine
Journal of Investigative Medicine MEDICINE, GENERAL & INTERNALMEDICINE, RESE-MEDICINE, RESEARCH & EXPERIMENTAL
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111
期刊介绍: Journal of Investigative Medicine (JIM) is the official publication of the American Federation for Medical Research. The journal is peer-reviewed and publishes high-quality original articles and reviews in the areas of basic, clinical, and translational medical research. JIM publishes on all topics and specialty areas that are critical to the conduct of the entire spectrum of biomedical research: from the translation of clinical observations at the bedside, to basic and animal research to clinical research and the implementation of innovative medical care.
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