Ontology highlight
ABSTRACT: Importance
Monogenic familial hypercholesterolemia (FH) is associated with lifelong elevations in low-density lipoprotein cholesterol (LDL-C) levels and increased risk of atherosclerotic cardiovascular disease (CVD). However, many individuals with hypercholesterolemia have a polygenic rather than a monogenic cause for their condition. It is unclear if a genetic variant for hypercholesterolemia alters the risk of CVD.Objectives
To assess whether a genetic variant for hypercholesterolemia alters the risk of atherosclerotic CVD and to evaluate how this risk compares with that of nongenetic hypercholesterolemia.Design, setting, and participants
In this genetic-association, case-control, cohort study, individuals aged 40 to 69 years were recruited by the UK Biobank from
SUBMITTER: Trinder M
PROVIDER: S-EPMC7042820 | biostudies-literature | 2020 Apr
REPOSITORIES: biostudies-literature