Gut microbiome and risk of ischaemic stroke: a comprehensive Mendelian randomization study

Author:

Meng Changjiang12,Deng Peizhi1,Miao Rujia2,Tang Haibo3,Li Yalan1,Wang Jie1,Wu Jingjing1,Wang Wei1,Liu Shiqi1,Xia Jian456,Lu Yao17ORCID

Affiliation:

1. Clinical Research Center, The Third Xiangya Hospital, Central South University , 138 Tongzipo Road, Changsha 410013 , China

2. Health Management Center, The Third Xiangya Hospital, Central South University , 138 Tongzipo Road, Changsha 410013 , China

3. Department of Metabolic and Bariatric Surgery, The Third Xiangya Hospital, Central South University , 138 Tongzipo Road, Changsha 410013 , China

4. Department of Neurology, Xiangya Hospital, Central South University , 87 Xiangya Road, Changsha 410008 , China

5. Clinical Research Center for Cerebrovascular Disease of Hunan Province, Central South University , 87 Xiangya Road, Changsha 410008 , China

6. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University , 87 Xiangya Road, Changsha 410008 , China

7. School of Life Course Sciences, King’s College London , Strand, London WC2R 2LS , UK

Abstract

Abstract Aims Increasing evidence implicates the microbiome as a susceptibility factor for ischaemic stroke (IS). Interpretation of this evidence is difficult, for the composition of the microbiome is influenced by various factors and might affect differently in IS subtypes. We aim to determine if the specific gut microbiome is causally associated with IS subtypes and suggest potential approaches for stroke prevention. Methods and results We conducted a two-sample Mendelian randomization (MR) analysis to test the causal relationship between gut microbiome and IS subtypes. For exposure data, we extracted genetic variants associated with 194 bacterial traits from MiBioGen consortium (n = 18 340). For outcomes, we selected three IS subtypes including cardioembolic stroke (CES, n = 410 484), small vessel stroke (SVS, n = 198 048), and large artery stroke (LAS, n = 198 048). Additionally, we performed a sequence of sensitivity analyses to validate preliminary MR results. There were four, three, and four bacteria showing an increased risk for LAS, SVS, and CES, respectively, and there were five, six, and five bacteria leading a decreasing risk for LAS, SVS, and CES, respectively. Amongst these, the genus_Intestinimonas showed negative associations with LAS [odds ratio (OR) = 0.77, 95% confidence interval (CI) (0.61–0.98)] and SVS (0.85, 0.73–0.98). The genus_LachnospiraceaeNK4A136group was genetically associated with decreased risk of both SVS (0.81, 0.66–0.99) and CES (0.75, 0.60–0.94). Conclusion The study revealed the causal effect of the abundance of specific bacterial features on the risk of IS subtypes. Notably, genus_Intestinimonas and genus_LachnospiraceaeNK4A136group displayed significant protection against more than one IS subtype, further suggesting potential applications of targeted probiotics in IS prevention.

Funder

National Key Research and Development Program

National Natural Science Foundation of China

Central South University Innovation-Driven Research Program

The Provincial Key Plan for Research and Development of Hunan

The Natural Science Foundation of Hunan Province

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

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