Ontology highlight
ABSTRACT: Background
Statins reduce low-density lipoprotein cholesterol (LDL-C) and are efficacious in the prevention of atherosclerotic cardiovascular disease (ASCVD). Dose-response to statins varies among patients and can be modeled using three distinct pharmacological properties: (1) E0 (baseline LDL-C), (2) ED50 (potency: median dose achieving 50% reduction in LDL-C); and (3) Emax (efficacy: maximum LDL-C reduction). However, individualized dose-response and its association with ASCVD events remains unknown.Objective
We analyze the relationship between ED50 and Emax with real-world cardiovascular disease outcomes.Method
We leveraged de-identified electronic health record data to identify individuals exposed to multipl
SUBMITTER: Aggarwal SK
PROVIDER: S-EPMC11086740 | biostudies-literature | 2024 Apr
REPOSITORIES: biostudies-literature