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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Therapeutic options to further lower C-reactive protein for patients on statin treatment
Parag H Joshi1, Terry A Jacobson
1Department of Medicine, Emory University, 69 Jesse Hill Jr Drive, Atlanta, GA 30303, USA. Parag.joshi@piedmont.org
Insights
This review examines high-sensitivity C-reactive protein (hsCRP) in statin trials. While some statin combinations affect hsCRP, evidence for improved cardiovascular risk reduction beyond statin monotherapy is currently lacking.
Area of Science:
- Cardiology
- Inflammation Biology
- Pharmacology
Background:
- Cardiovascular disease (CVD) is a primary cause of death globally.
- Inflammation is recognized as a key factor in CVD development.
- High-sensitivity C-reactive protein (hsCRP) is a biomarker linked to cardiovascular risk.
Purpose of the Study:
- To review hsCRP changes in major statin outcome trials.
- To explore the concept of targeting both low-density lipoprotein cholesterol (LDL-C) and hsCRP.
- To assess the impact of statin combination therapies on hsCRP levels.
Main Methods:
- Review of results from major statin outcome trials focusing on hsCRP.
- Analysis of studies evaluating combination therapies (statin + ezetimibe, fenofibric acid, niacin, colesevelam) and their effect on hsCRP.
- Examination of existing evidence regarding cardiovascular risk reduction with combination therapies.
Main Results:
- Statin trials show a correlation between hsCRP levels and cardiovascular risk.
- Some statin combination therapies demonstrate additional effects on hsCRP and other lipids.
- Current evidence does not conclusively support cardiovascular risk reduction benefits of combination therapies over statin monotherapy.
Conclusions:
- Further placebo-controlled trials are needed to clarify the role of targeting hsCRP versus LDL-C for cardiovascular risk reduction.
- Current evidence suggests prioritizing low-density lipoprotein cholesterol (LDL-C) targets in managing cardiovascular risk.
- The clinical significance of hsCRP reduction beyond LDL-C lowering by combination therapies remains to be established.
Abstract:
Cardiovascular disease remains the leading cause of morbidity and mortality in developed nations. Inflammation plays an increasingly important role in the cardiovascular disease process. Recent statin trials have demonstrated a correlation between the inflammatory biomarker high-sensitivity C-reactive protein (hsCRP) and cardiovascular risk. This review describes the results of changes in hsCRP in the major statin outcome trials and the concept of a "dual target" for both low-density lipoprotein cholesterol and hsCRP. The effect on hsCRP of combination statin therapy with ezetimibe, fenofibric acid, niacin, and colesevelam is reviewed. Although some statin combination therapies have additional effects on CRP and other atherogenic lipids, evidence for their effect on cardiovascular risk beyond statin monotherapy is lacking. Ongoing placebo-controlled trials investigating statin combination therapy versus statin monotherapy may provide additional clues to the role of additional changes in lipids versus markers of inflammation on cardiovascular risk reduction. Until these trials are completed, current evidence suggests focusing on low-density lipoprotein cholesterol targets.
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