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Updated: May 5, 2026

Intrastriatal Injection of Autologous Blood or Clostridial Collagenase as Murine Models of Intracerebral Hemorrhage
Published on: July 3, 2014
Gut Microbiome variation in patients with early-stage mild-to-moderate intracerebral hemorrhage: A pilot study
Haixiao Jiang1, Wei Zeng2, Xiaoli Zhang3
1Department of Neurosurgery, The Affiliated Hospital of Yangzhou University, Yangzhou 225009, China.
Background:
The significant morbidity and mortality rates of acute intracerebral hemorrhage (ICH) are well-known around the world. The link between gut microbiota and different types of strokes is becoming more studied. The goal of this study was to look at the relationships between intestinal flora and early-stage mild-to-moderate ICH (emICH), and to provide a new perspective for adjunctive treatment of emICH.
Methods:
Fecal samples from 100 participants with emICH (n=50) and healthy individuals (n=50) in this study were collected as well as analyzed utilizing 16S rRNA gene amplicon sequencing in order to characterize the gut microbial community.
Results:
Distinct microbial communities are present within each group, with emICH patients exhibiting a diminished diversity and uniformity in their microbial profiles. A notable shift in the gut microbiota composition of emICH patients has been observed, characterized by an upsurge in pro-inflammatory microbes belonging to the Euryarchaeota phylum and a concurrent decline in beneficial Bacteroidetes species. Concurrently, significant associations and patterns among operational taxonomic units (OTUs) were identified in emICH patients. A panel of biomarkers (WAL_1855D, Methanobrevibacter, Streptococcus, Bacteroides, Coprococcus, Lachnospira) has been effectively utilized to distinguish emICH patients from healthy individuals, with an area under the curve (AUC) of 0.845. Additionally, an analysis using the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway annotation uncovered several perturbed pathways in emICH patients, predominantly those related to metabolic processes and the inflammatory response. Moreover, predictive profiling of the microbiome's phenotypic traits suggests that emICH patients are likely to harbor a higher prevalence of Gram-negative bacteria and potential opportunistic pathogens compared to healthy controls.
Conclusions:
The gut microbiota ecosystem of emICH patients is disrupted, characterized primarily by an increase in pro-inflammatory microbiota, elevated inflammatory signaling pathways, and metabolic dysregulation. Furthermore, microbiota modulation may be seen as a novel approach for the adjunctive treatment of emICH.
Insights
Gut microbiota alterations are linked to early-stage mild-to-moderate intracerebral hemorrhage (emICH). This study found disrupted gut bacteria in emICH patients, suggesting microbiota modulation as a potential adjunctive treatment.
Area of Science:
- Microbiome research
- Neurology
- Gastroenterology
Background:
- Acute intracerebral hemorrhage (ICH) causes significant global morbidity and mortality.
- Emerging research highlights the connection between gut microbiota and stroke incidence.
- Understanding these gut-brain axis interactions is crucial for novel therapeutic strategies.
Purpose of the Study:
- To investigate the relationship between gut microbiota composition and early-stage mild-to-moderate ICH (emICH).
- To identify specific microbial biomarkers for emICH detection.
- To explore the potential of microbiota modulation as an adjunctive therapy for emICH.
Main Methods:
- 16S rRNA gene amplicon sequencing was used to analyze fecal samples from 50 emICH patients and 50 healthy controls.
- Operational taxonomic units (OTUs) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were analyzed.
- Biomarker panels were identified for distinguishing between emICH patients and healthy individuals.
Main Results:
- emICH patients exhibited reduced gut microbial diversity and uniformity compared to controls.
- A significant increase in pro-inflammatory Euryarchaeota and a decrease in beneficial Bacteroidetes were observed in emICH patients.
- A biomarker panel (WAL_1855D, Methanobrevibacter, Streptococcus, Bacteroides, Coprococcus, Lachnospira) achieved an AUC of 0.845 for emICH detection. Perturbed KEGG pathways included inflammation and metabolic processes. emICH patients showed a higher prevalence of Gram-negative bacteria.
Conclusions:
- The gut microbiota in emICH patients is dysbiotic, with increased pro-inflammatory microbes and dysregulated inflammatory and metabolic pathways.
- Microbiota modulation presents a promising avenue for adjunctive treatment strategies in emICH.
- Targeting the gut microbiome could offer new therapeutic approaches for improving outcomes in emICH patients.
Related Concept Videos
Introduction to the Human Microbiota
Development of Human Microbiota
Gut-Brain Axis

