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Published on: November 10, 2017
Nonstatin therapies for management of dyslipidemia: a review
Karen R Sando1, Michelle Knight1
1College of Pharmacy, Department of Pharmacotherapy & Translational Research, University of Florida, Gainesville, Florida.
Insights
Nonstatin therapies offer limited cardiovascular benefits when added to statins. However, they may be useful for patients intolerant to statins or with specific lipid profiles, warranting further research.
Area of Science:
- Cardiology
- Pharmacology
- Preventive Medicine
Background:
- Cardiovascular disease (CVD) is a leading cause of death in the US.
- Statins are the primary treatment for CVD prevention, but optimal strategies for statin-intolerant patients or those needing additional lipid lowering are unclear.
- Recent evidence questions the benefit of combination therapy.
Purpose of the Study:
- To review evidence on nonstatin drugs for reducing cardiovascular outcomes.
- To provide clinical recommendations for nonstatin therapy use.
- To discuss emerging nonstatin treatments for dyslipidemia.
Main Methods:
- Searched PubMed, International Pharmaceutical Abstracts, and Cochrane Database.
- Included English-language human clinical trials, meta-analyses, and systematic reviews.
- Used keywords: niacin, omega-3 FAs, fibrates, bile acid sequestrants, ezetimibe, PCSK9, CETP inhibitors.
Main Results:
- Niacin and omega-3 FAs showed no benefit in combination trials.
- Fibrates may benefit patients with high triglycerides or low HDL-C when combined with statins.
- Ezetimibe-statin therapy improved outcomes in specific high-risk groups; emerging therapies (PCSK9, CETP) are under evaluation.
Conclusions:
- Nonstatin therapies have a limited role alongside guideline-directed statin therapy.
- Consider nonstatins for statin-intolerant patients, those with severe hypertriglyceridemia, or high cardiovascular risk.
- Further research is needed on nonstatin use in patients unable to tolerate guideline-directed statin doses.
Purpose:
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in the United States. Recently published cholesterol treatment guidelines emphasize the use of statins as the preferred treatment strategy for both primary and secondary prevention of CVD. However, the optimal treatment strategy for patients who cannot tolerate statin therapy or those who need additional lipid-lowering therapy is unclear in light of recent evidence that demonstrates a lack of improved cardiovascular outcomes with combination therapy. The purpose of this review is to summarize and interpret evidence that evaluates nonstatin drug classes in reducing cardiovascular outcomes, to provide recommendations for use of nonstatin therapies in clinical practice, and to review emerging nonstatin therapies for management of dyslipidemia.
Methods:
Relevant articles were identified through searches of PubMed, International Pharmaceutical Abstracts, and the Cochrane Database of Systematic Reviews by using the terms niacin, omega-3 fatty acids (FAs), clofibrate, fibrate, fenofibrate, fenofibric acid, gemfibrozil, cholestyramine, colestipol, colesevelam, ezetimibe, proprotein convertase subtilisin/kexin 9 (PCSK9), cholesteryl ester transfer protein (CETP), and cardiovascular outcomes. Only English language, human clinical trials, meta-analyses, and systematic reviews were included. Additional references were identified from citations of published articles.
Findings:
Niacin may reduce cardiovascular events as monotherapy; however, recent trials in combination with statins have failed to show a benefit. Trials with omega-3 FAs have failed to demonstrate significant reductions in cardiovascular outcomes. Fibrates may improve cardiovascular outcomes as monotherapy; however, trials in combination with statins have failed to show a benefit, except in those with elevated triglycerides (>200 mg/dL) or low HDL-C (<40 mg/dL). There is a lack of data that evaluates bile acid sequestrant in combination with statin therapy on reducing cardiovascular events. Ezetimibe-statin combination therapy can reduce cardiovascular outcomes in those with chronic kidney disease and following vascular surgery or acute coronary syndrome. Long-term effects of emerging nonstatin therapies (CETP and PCSK9 inhibitors) are currently being evaluated in ongoing Phase III trials.
Implications:
Nonstatin therapies have a limited role in reducing cardiovascular events in those maintained on guideline-directed statin therapy. In certain clinical situations, such as patients who are unable to tolerate statin therapy or recommended intensities of statin therapy, those with persistent severe elevations in triglycerides, or patients with high cardiovascular risk, some nonstatin therapies may be useful in reducing cardiovascular events. Future research is needed to evaluate the role of nonstatin therapies in those who are unable to tolerate guideline-directed statin doses.
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