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Microbiome signatures in ischemic stroke: A systematic review. | LitMetric

Microbiome signatures in ischemic stroke: A systematic review.

Heliyon

The First School of Clinical Medicine, Lanzhou University, Lanzhou, China.

Published: January 2024

AI Article Synopsis

  • Microbial changes are linked to cerebral ischemia, influencing stroke development.
  • A systematic review analyzed 24 studies and found key bacterial phyla present in both stroke patients and healthy individuals.
  • Significant differences in microbial diversity were identified in stroke patients compared to non-stroke individuals, suggesting an imbalance that affects stroke severity and outcomes.
  • Further research is necessary to better understand how the microbiome impacts ischemic stroke.

Article Abstract

Microbial structural changes and dysfunction play an important role in the development of cerebral ischemia. We searched PubMed, Embase, Web of Science, and Cochrane Library and conducted a systematic review to assess the relationship between the human microbiome and ischemic stroke. A total of 24 studies were included, and the intestinal bacterial communities detected in both stroke and healthy people were dominated by 4 main phyla, including Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria. Significant diversity (alpha and beta) in patients with ischemic versus nonischemic stroke was observed in nine out of 18 studies, and 3 studies showed that the severity of ischemic stroke affected microbial diversity. The imbalance of bacteria that produce short-chain fatty acids (SCFAs) changes the bacterial metabolic pathway, and disorders in the level of bacterial metabolites (trimethylamine N-oxide TMAO) lead to significant changes in intestinal flora function, which may aggravate the severity of stroke and affect its prognosis. Further studies are needed to explore the relationship between the microbiome and ischemic stroke.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10772200PMC
http://dx.doi.org/10.1016/j.heliyon.2023.e23743DOI Listing

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