Ontology highlight
ABSTRACT: Background
von Willebrand factor (VWF) multimers are cleaved by A disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS-13) into less active fragments. Thrombospondin 1 (TSP-1) competes with VWF's cleavage site, protecting it from degradation. Low ADAMTS-13 and high VWF have been associated with cardiovascular disease and atrial fibrillation (AF).Objectives
We aimed to investigate whether VWF, ADAMTS-13, and TSP-1 are associated with clinical outcome.Methods
Elderly patients with a recent myocardial infarction (MI) (n = 1027) were followed for 2 years. Blood was collected 2 to 8 weeks after the MI for ADAMTS-13, VWF, and TSP-1 measures. The primary endpoints (major adverse cardiovascular events; n = 210) included the first event of MI
SUBMITTER: Warlo EMK
PROVIDER: S-EPMC10225923 | biostudies-literature | 2023 May
REPOSITORIES: biostudies-literature