Inflammatory biomarkers in infective endocarditis: machine learning to predict mortality
T Ris1,2, A Teixeira-Carvalho3, R Matos Pinto Coelho1
1Programa de Pós-Graduação em Infectologia e Medicina Tropical e Departamento de Clínica Médica, Faculdade de Medicina da Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Clinical and Experimental Immunology
|January 31, 2019
Summary
New biomarkers are needed for infective endocarditis (IE) mortality. Interleukin-15 (IL-15) and C-C motif chemokine ligand (CCL4) predict death, improving risk stratification beyond C-reactive protein (CRP).
Area of Science:
- Cardiology
- Immunology
- Biomarker Discovery
Background:
- Infective endocarditis (IE) has high mortality rates.
- Improved patient management requires novel biomarkers for risk stratification.
- Current prognostic tools may not fully capture IE patient risk.
Purpose of the Study:
- To investigate if cytokines, chemokines, and growth factors at diagnosis predict mortality in IE patients.
- To identify novel biomarkers that enhance risk prediction beyond C-reactive protein (CRP).
- To develop a predictive model for IE patient outcomes using machine learning.
Main Methods:
- Analysis of 27 cytokines, chemokines, and growth factors using Luminex assay in 69 IE patients.
- Application of machine learning techniques to predict mortality.
- Development of a decision tree incorporating biomarker levels and CRP for risk stratification.
Main Results:
- In-hospital mortality was 26%.
- Interleukin-15 (IL-15) and C-C motif chemokine ligand (CCL4) significantly predicted death.
- A decision tree model achieved 91% accuracy in outcome prediction.
- High-risk group (elevated CRP, IL-15, CCL4) had 88% mortality; low-risk had 8% mortality.
Conclusions:
- Cytokines IL-15 and CCL4 are valuable predictors of mortality in IE.
- These biomarkers offer prognostic value beyond CRP levels.
- Assessing cytokines holds potential for clinical risk stratification and monitoring of IE patients.
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