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A Machine-Learning Model for the Prognostic Role of C-Reactive Protein in Myocarditis
Anna Baritussio1, Chun-Yan Cheng1, Giulia Lorenzoni2
1Cardiology, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, 35128 Padua, Italy.
C-reactive protein (CRP) levels at diagnosis in myocarditis patients indicate less severe clinical features, particularly in clinically suspected cases. However, CRP does not predict patient survival, which is primarily linked to ejection fraction and biopsy-proven status.
Area of Science:
- Cardiology
- Inflammation
- Biomarkers
Background:
- The role of inflammation markers, such as C-reactive protein (CRP), in diagnosing and predicting outcomes for myocarditis remains unclear.
- Understanding these markers is crucial for effective patient management and prognosis.
Purpose of the Study:
- To evaluate the diagnostic and prognostic significance of C-reactive protein (CRP) levels at the time of diagnosis in patients with myocarditis.
- To identify predictors of mortality and heart transplant (Htx) in this patient cohort.
Main Methods:
- Retrospective analysis of 409 patients with clinically suspected (CS) or biopsy-proven (BP) myocarditis, with available CRP data at diagnosis.
- Machine learning (random forest) was used to analyze survival data and identify predictors of death/Htx.
- Clinical, laboratory, and imaging data were collected at diagnosis and follow-up.
Main Results:
- Abnormal CRP levels were more frequent in CS myocarditis, associated with recent viral infection, shorter symptom duration, chest pain, better functional class, and higher troponin I.
- There were 13 deaths/Htx events over a median follow-up of 2.9 years (10-year survival 94%), with 10 occurring in BP myocarditis patients.
- CRP levels did not significantly differ survival rates (p = 0.23).
Conclusions:
- Elevated CRP at diagnosis is associated with less severe clinical presentations in CS myocarditis but does not predict survival.
- The strongest predictors of death/Htx were reduced left ventricular ejection fraction (LVEF), biopsy-proven myocarditis, and positive anti-nuclear auto-antibodies (ANA).
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