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Published on: November 10, 2017
Recent Updates in Hypertriglyceridemia Management for Cardiovascular Disease Prevention
Renato Quispe1, Ty Sweeney1, Bhavya Varma1
1Ciccarone Center for the Prevention of Cardiovascular Disease, Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Blalock 524-C, Baltimore, MD, 21287, USA.
High-dose icosapent ethyl (EPA) reduces vascular events in high-risk patients with elevated triglycerides on statin therapy. Novel therapies targeting triglyceride-rich lipoproteins are under investigation for residual ASCVD risk.
Area of Science:
- Cardiology
- Metabolic Diseases
- Pharmacology
Background:
- Triglyceride-rich lipoproteins (TRL) play a causal role in atherosclerotic cardiovascular disease (ASCVD).
- Residual ASCVD risk persists in patients with elevated triglycerides despite statin therapy for LDL-C reduction.
Purpose of the Study:
- To review current evidence on triglyceride-lowering therapies for managing hypertriglyceridemia and residual ASCVD risk.
- To evaluate the efficacy and safety of various pharmacological interventions beyond statins.
Main Methods:
- Review of randomized clinical trials and emerging research on triglyceride-lowering agents.
- Analysis of data from key trials like REDUCE-IT and studies on fibrates, apoC3, and ANGPTL3 inhibitors.
Main Results:
- Icosapent ethyl (highly purified EPA) demonstrated significant reduction in vascular events in high-risk patients.
- Fibrates show no incremental ASCVD benefit with statins but are useful for pancreatitis prevention.
- Emerging therapies like apoC3 and ANGPTL3 inhibitors show promise in reducing triglycerides and LDL-C.
Conclusions:
- High-dose icosapent ethyl offers cardiovascular benefit in statin-treated patients with elevated triglycerides and high ASCVD risk.
- Novel selective therapies targeting TRL metabolism are a promising area for future ASCVD risk reduction.
- Management of hypertriglyceridemia remains crucial for addressing residual cardiovascular risk.
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