Background: Alterations in the gut microbiota after ischemic stroke have been demonstrated, whereas the effect on stroke outcome remains to be established.
Methods: A total of 132 consecutive patients with acute ischemic stroke were prospectively enrolled. Their gut microbiomes within 24 h of admission were profiled using 16S ribosomal RNA (rRNA) gene (V3-V4 region) sequencing. Microbiota comparisons were made between groups with good outcome ( = 105) and poor outcome ( = 27) based on 3-month modified Rankin Scale scores of 0-2 and 3-6. Propensity score-matching (PSM) analysis was conducted to assess the robustness of our findings. The functional potential was predicted using the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt).
Results: Patients in the poor outcome group were characterized by a significant reduction in the alpha diversity (Shannon index, = 0.025; Simpson index, = 0.010), an increase in the pathogenic bacteria (e.g., and ), and a decrease in the short-chain fatty acids (SCFAs)-producing bacteria (e.g., , and ) to those with good outcome group (all < 0.05). Similar results of microbial composition were obtained after PSM. The PICRUSt revealed that the pathway for membrane transport was relatively dominant in patients with poor outcome ( < 0.05).
Conclusion: This study demonstrated that stroke patients with 3-month poor outcome had baseline gut microbiota dysbiosis featured by increased pathogenic bacteria and decreased SCFAs-producing bacteria.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831883 | PMC |
http://dx.doi.org/10.3389/fneur.2021.799222 | DOI Listing |
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