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Published on: November 10, 2017
Choosing the optimal nonstatin lipid-lowering therapies for statin-intolerant patients: A systematic review and
Wattakorn Laohapiboolrattana1, Paisit Kosum2, Mantiwee Nimworapan3
1Division of Neurology, Department of Medicine, Faculty of Medicine, Naresuan University, Phitsanulok, Thailand (Dr. Laohapiboolrattana and Roongpiboonsopit).
Background:
Statin intolerance presents a considerable challenge in managing patients at risk for cardiovascular diseases, as it limits patients' access to standard lipid-lowering therapies.
Objective:
This study aims to compare the efficacy and safety of various nonstatin lipid-lowering therapies in patients who are intolerant to statins.
Methods:
We searched PubMed, Embase, CENTRAL, and EBSCO open dissertations through September 2023 for randomized controlled trials in statin-intolerant patients comparing nonstatin lipid-lowering agents. The primary outcome was low-density lipoprotein cholesterol (LDL-C). A random-effects model estimated comparative effects using mean differences (MDs) for LDL-C reduction and relative risks (RRs) for safety outcomes, specifically trial withdrawal due to adverse events. Results were reported with 95% CIs, and therapies ranked using the surface under the cumulative ranking curve (SUCRA). Evidence certainty was assessed with the Confidence in Network Meta-Analysis (CINeMA) platform.
Results:
Of 1533 articles, 6 studies (1326 patients) met inclusion criteria. Evolocumab combined with ezetimibe achieved the greatest LDL-C reduction (MD: 48.98%; 95% CI: 59.19, -38.77) vs ezetimibe alone, with moderate evidence certainty. Evolocumab, alirocumab, and the combination of bempedoic acid and ezetimibe, also showed significant reductions in LDL-C compared to ezetimibe monotherapy, though the magnitude of their effects was smaller than that of the evolocumab and ezetimibe combination. The SUCRA of evolocumab and ezetimibe (99.7%) aligns with its highest comparative efficacy. No significant differences in safety outcomes were observed across treatments.
Conclusion:
Evolocumab combined with ezetimibe is the most effective regimen for LDL-C reduction, with a safety profile comparable to other treatments, making it a viable alternative for patients with statin intolerance.
Insights
For patients intolerant to statins, combining evolocumab with ezetimibe offers the most effective LDL-C reduction. This combination demonstrates a comparable safety profile to other non-statin therapies, providing a viable alternative for cardiovascular risk management.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Statin intolerance poses a significant challenge in managing cardiovascular disease risk.
- It limits patient access to effective standard lipid-lowering therapies.
Purpose of the Study:
- To compare the efficacy and safety of non-statin lipid-lowering therapies.
- Focus on patients with statin intolerance.
Main Methods:
- Systematic search of PubMed, Embase, CENTRAL, and EBSCO open dissertations up to September 2023.
- Network meta-analysis of randomized controlled trials comparing non-statin agents.
- Primary outcome: low-density lipoprotein cholesterol (LDL-C) reduction; secondary outcome: safety events.
Main Results:
- Evolocumab plus ezetimibe showed the greatest LDL-C reduction (48.98%) versus ezetimibe alone, with moderate certainty.
- Other effective non-statin therapies included evolocumab, alirocumab, and bempedoic acid/ezetimibe combination.
- No significant differences in safety outcomes (adverse events) were observed across treatments.
Conclusions:
- Evolocumab combined with ezetimibe is the most effective regimen for reducing LDL-C in statin-intolerant patients.
- This combination presents a safe and viable alternative to statins for managing hyperlipidemia and cardiovascular risk.
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