| Literature DB >> 34711341 |
Robert S Rosenson1, Aleesha Shaik2, Wenliang Song3.
Abstract
Emerging evidence suggests that elevated concentrations of triglyceride-rich lipoprotein remnants (TRLs) derived from hepatic and intestinal sources contribute to the risk of atherosclerotic cardiovascular events. Natural selection studies support a causal role for elevated concentrations of remnant cholesterol and the pathways contributing to perturbations in metabolic pathways regulating TRLs with an increased risk of atherosclerotic cardiovascular disease events. New therapies targeting select catalytic pathways in TRL metabolism reduce atherosclerosis in experimental models, and concentrations of TRLs in patients with a vast range of triglyceride levels. Clinical trials with inhibitors of angiopoietin-like 3 protein and apolipoprotein C-III will be required to provide further guidance on the potential contribution of these emerging therapies in the paradigm of cardiovascular risk management in patients with elevated remnant cholesterol.Entities:
Keywords: angiopoietin-like 3 protein inhibitors; apolipoprotein C-III inhibitors; eicosapentaenoic acid; omega-3 fatty acids; triglyceride-rich lipoproteins; triglycerides
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Year: 2021 PMID: 34711341 PMCID: PMC9327673 DOI: 10.1016/j.jacc.2021.08.051
Source DB: PubMed Journal: J Am Coll Cardiol ISSN: 0735-1097 Impact factor: 27.203