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Circulating biomarkers and gut microbiota profiling predict post-stroke infection in acute ischemic stroke patients.

Circulating biomarkers and gut microbiota profiling predict post-stroke infection in acute ischemic …
Photo by CDC / Unsplash
Key Takeaway
Consider combined biomarker and microbiota models for post-stroke infection risk stratification in acute ischemic stroke patients.

This prospective observational study assessed 80 acute ischemic stroke patients admitted within 24 h of onset at Prof. Dr. dr. Mahar Mardjono National Brain Center Hospital, Jakarta, with a 7 days follow-up period duration. The investigation focused on circulating biomarkers including NMDAR, butyrate, TMAO, RANKL, iFABP, and LPS alongside gut microbiota profiling via 16S rRNA sequencing analysis.

Post-stroke infection occurred in 37/80 patients, representing 46.3% of the cohort. NMDAR demonstrated the highest diagnostic performance with an AUC of 0.911, sensitivity of 86.5%, and specificity of 90.7. Other biomarkers included iFABP (AUC 0.894), LPS (AUC 0.896), RANKL (AUC 0.881), butyrate (AUC 0.866), and TMAO (AUC 0.865). Multivariate models integrating microbiota features and biomarkers showed improved predictive accuracy compared with single-domain approaches for the primary outcome of post-stroke infection.

Infected patients exhibited reduced evenness and dominance imbalance. Pathogenic taxa such as Escherichia coli and Salmonella enterica were enriched, while commensals like Faecalibacterium prausnitzii and Roseburia intestinalis were depleted. Safety data regarding adverse events, serious adverse events, and discontinuations were not reported in the study protocol. The study design limits causal inference and generalizability to other settings.

Practice relevance supports combined biomarker–microbiota models for risk stratification and preventive strategies. However, the single-center nature and observational design require validation in broader populations before clinical implementation can be considered.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundPost-stroke infection (PSI), particularly pneumonia and urinary tract infection, is a common and serious complication after acute ischemic stroke (AIS). Current diagnostic biomarkers provide limited accuracy when used in isolation. This study aimed to evaluate the diagnostic value of circulating biomarkers and gut microbiota profiling, both individually and in combination, to predict PSI in AIS patients.MethodsWe conducted a prospective observational study at Prof. Dr. dr. Mahar Mardjono National Brain Center Hospital, Jakarta. A total of 80 AIS patients admitted within 24 h of onset were enrolled and followed for 7 days to assess PSI. Blood samples were analyzed for NMDAR, butyrate, TMAO, RANKL, iFABP, and LPS. Stool samples were collected for 16S rRNA sequencing. Diagnostic performance was evaluated using ROC curves, with AUC, sensitivity, and specificity calculated. Multivariate logistic regression models were constructed to assess independent predictors and combined diagnostic accuracy.ResultsPSI occurred in 37/80 patients (46.3%). NMDAR showed the highest diagnostic performance (AUC 0.911; sensitivity 86.5%; specificity 90.7), followed by iFABP (AUC 0.894), LPS (AUC 0.896), RANKL (AUC 0.881), butyrate (AUC 0.866), and TMAO (AUC 0.865). Gut microbiota analysis revealed reduced evenness and dominance imbalance in infected patients, with enrichment of pathogenic taxa (Escherichia coli, Salmonella enterica) and depletion of SCFA-producing commensals (Faecalibacterium prausnitzii, Roseburia intestinalis). Multivariate models integrating microbiota features and biomarkers improved predictive accuracy compared with single-domain approaches.ConclusionIntegrating circulating biomarkers with gut microbiota profiling significantly enhances early prediction of PSI in AIS. These findings highlight the role of the gut–brain–immune axis in post-stroke complications and support combined biomarker–microbiota models for risk stratification and preventive strategies.
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