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Updated: Aug 31, 2025

A Data-Driven Approach to Quantifying Immune States in Sepsis
Published on: February 7, 2025
Application of Machine Learning for Clinical Subphenotype Identification in Sepsis
Chang Hu1,2, Yiming Li1,2, Fengyun Wang1,2
1Department of Critical Care Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, Hubei, China.
Introduction:
Sepsis is a heterogeneous clinical syndrome. Identification of sepsis subphenotypes could lead to allowing more precise therapy. However, there is a lack of models to identify the subphenotypes in such patients. Thus, we aimed to identify possible subphenotypes and compare the clinical outcomes for subphenotypes in a large sepsis cohort.
Methods:
This machine learning-based, cluster analysis was performed using the Medical Information Mart in Intensive Care (MIMIC)-IV database. We enrolled all adult (> 18 years old) patients diagnosed with sepsis in the first 24 h after intensive care unit (ICU) admission. K-means cluster analysis was performed to identify the number of classes. Multivariable logistic regression models were used to estimate the association between sepsis subphenotypes and in-hospital mortality.
Results:
A total of 8817 participants with sepsis were enrolled. The median age was 66.8 (IQR, 55.9-77.1) years, and 38.1% (3361/8817) were female. Two subphenotypes resulted in optimal separation including 11 routinely available clinical variables obtained during the first 24 h after ICU admission. Participants in subphenotype B showed higher levels of lactate, glucose and creatinine, white blood cell count, sodium and heart rate and lower body temperature, platelet count, systolic blood pressure, hemoglobin and PaO2/FiO2 ratio. In addition, the in-hospital mortality in patients with subphenotype B was significantly higher than that in subphenotype A (29.4% vs. 8.5%, P < 0.001). The difference was still significant after adjustment for potential covariates (adjusted OR 2.214; 95% CI 1.780-2.754, P < 0.001).
Conclusions:
Two sepsis subphenotypes with different clinical outcomes could be rapidly identified using the K-means clustering analysis based on routinely available clinical data. This finding may help clinicians to identify the subphenotype rapidly at the bedside.
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