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ABSTRACT: Background
Cardiovascular diseases (CVD) remain the leading cause of morbidity and mortality globally. Traditional risk models, primarily based on established risk factors, often lack the precision needed to accurately predict new-onset major adverse cardiovascular events (MACE). This study aimed to improve prediction and risk stratification by integrating traditional risk factors with biochemical and metabolomic biomarkers.Methods
We analyzed data from 229,352 participants in the UK Biobank (median age 58.0 years; 45.4% male) who were free of baseline MACE. Biomarker selection was conducted using area under the curve (AUC), minimal joint mutual information maximization (JMIM), and correlation analyses, while Cox proportional hazards models were employed to evaluate the pre
SUBMITTER: Zhang XR
PROVIDER: S-EPMC11966882 | biostudies-literature | 2025 Apr
REPOSITORIES: biostudies-literature