Incremental value of a gut microbiome score (M-score) for predicting stroke-associated pneumonia beyond the clinical
Yidan Zhang1, Qi Dong2, Wenbin Li3
11Department of Emergency Medicine, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai City, 519000, Guangdong Province, China.
Abstract:
Stroke-associated pneumonia (SAP) is a major complication of acute ischemic stroke. The brain-gut-lung axis suggests that post-stroke gut dysbiosis may offer independent risk information beyond clinical scores like A2DS2. The aim of this study was to evaluate the incremental predictive value of early post-stroke gut microbiome biomarkers for SAP and to construct a simplified microbiome risk score (M-score). In a prospective nested case-control study, we identified 63 SAP cases from a cohort of 551 patients with acute ischemic stroke and stool samples were collected 24-72 h post-admission. Cases were matched 1:2 (age, sex) to 126 controls. Gut microbiota was profiled via 16S rRNA sequencing. Three differentially abundant genera (prevalence ≥20%, FDR q < 0.10) were used to construct an M-score via bootstrapped regression. Independent associations were assessed with conditional logistic regression. Incremental value over the A2DS2 score was evaluated using AUC, continuous net reclassification improvement (NRI), and the Brier score. SAP cases exhibited reduced α-diversity and distinct β-diversity (both P < 0.01). Cases had higher Enterococcus and Streptococcus and lower Faecalibacterium levels (all q < 0.05). The M-score was independently associated with SAP (adjusted OR per 1-SD: 1.76, 95% CI: 1.30-2.39, P = 0.001). Adding the M-score to A2DS2 significantly improved prediction: AUC increased from 0.76 to 0.84 (ΔAUC = 0.08, P = 0.009), NRI was 0.31 (95% CI: 0.12-0.51), and the Brier score decreased from 0.18 to 0.16. Results were robust in sensitivity analyses. A gut microbiome score based on three genera provides significant independent and incremental predictive value for SAP over the A2DS2 score, enabling more precise early risk stratification after stroke.
Insights
A novel microbiome risk score (M-score) can predict stroke-associated pneumonia (SAP) risk. This gut microbiome analysis offers better prediction than existing clinical scores, improving early risk stratification for stroke patients.
Area of Science:
- Neurology
- Microbiology
- Pulmonology
Background:
- Stroke-associated pneumonia (SAP) is a significant complication following acute ischemic stroke.
- The brain-gut-lung axis highlights the gut microbiome's potential role in post-stroke complications.
- Existing clinical scores may not fully capture SAP risk, necessitating novel biomarkers.
Purpose of the Study:
- To assess the incremental predictive value of early gut microbiome biomarkers for SAP.
- To develop a simplified microbiome risk score (M-score) for SAP prediction.
- To evaluate the M-score's performance against the established A2DS2 clinical score.
Main Methods:
- Prospective nested case-control study of 551 acute ischemic stroke patients.
- Stool sample analysis (16S rRNA sequencing) within 24-72 hours of admission.
- Development of an M-score using three differentially abundant gut genera and logistic regression.
Main Results:
- SAP cases showed reduced gut microbial diversity and distinct community composition.
- Higher levels of Enterococcus and Streptococcus, and lower Faecalibacterium were observed in SAP cases.
- The M-score independently predicted SAP and significantly improved prediction accuracy when added to the A2DS2 score (AUC increased from 0.76 to 0.84).
Conclusions:
- Gut microbiome profiling can identify early SAP risk in stroke patients.
- The M-score offers significant independent and incremental predictive value for SAP.
- This microbiome-based approach enhances early risk stratification for SAP post-stroke.
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