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Published on: November 10, 2017
Lipid-modifying efficacy and safety of obicetrapib in high-risk cardiovascular patients: A systematic review and
Abdul Mueez Alam Kayani1, Muhammad Faiq Umar1, Daniel Navarro-Martinez2
1Department of Internal Medicine, AdventHealth Tampa, Tampa, FL, United States of America.
Insights
Obicetrapib significantly improves lipid profiles, lowering LDL-C and Lp(a) while increasing HDL-C in high-risk Atherosclerotic Cardiovascular Disease patients. This cholesteryl ester transfer protein inhibitor showed no increased short-term adverse events in a recent meta-analysis.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Lipid Metabolism
Background:
- Atherosclerotic cardiovascular disease (ASCVD) is a major cause of death, with many high-risk patients failing to reach target low-density lipoprotein cholesterol (LDL-C) levels despite therapy.
- Obicetrapib, a cholesteryl ester transfer protein (CETP) inhibitor, modifies lipoprotein profiles by inhibiting cholesterol ester transfer.
Purpose of the Study:
- To evaluate the efficacy and safety of obicetrapib as an add-on therapy for high-risk ASCVD patients.
- To assess obicetrapib's impact on various lipid parameters and adverse events.
Main Methods:
- A systematic literature search was conducted across online databases.
- Outcomes included percentage changes in LDL-C, HDL-C, non-HDL-C, triglycerides, ApoB, and lipoprotein (a) [Lp(a)].
- Risk ratios and mean differences with 95% confidence intervals were calculated for categorical and continuous outcomes, respectively.
Main Results:
- Analysis of three studies involving 3088 patients revealed significant reductions in LDL-C (-31.75%), non-HDL-C (-29.35%), Lp(a) (-35.67%), and ApoB (-19.37%).
- Obicetrapib markedly increased HDL-C (+125.94%) with no significant change in total cholesterol or triglycerides.
- No increased risk of adverse events, discontinuation, acute kidney injury, liver enzyme elevation, creatine kinase elevation, or hypertension was observed.
Conclusions:
- Obicetrapib substantially improved lipid profiles in high-risk ASCVD patients receiving maximally tolerated lipid-lowering therapy.
- The drug demonstrated a favorable short-term safety profile.
- Long-term randomized studies are necessary to confirm sustained efficacy and safety, and to evaluate clinical cardiovascular outcomes.
Introduction:
Atherosclerotic cardiovascular disease (ASCVD) remains a leading cause of morbidity and mortality, particularly among high-risk patients. Despite the availability of multiple lipid lowering therapies, many patients fail to achieve the guideline recommended low-density lipoprotein cholesterol (LDL-C) targets. Obicetrapib, a cholesteryl ester transfer protein (CETP) inhibitor optimizes lipid profile by blocking the exchange of cholesterol esters from high-density lipoprotein cholesterol (HDL-C) to Apolipoprotein B (ApoB) containing lipoproteins. This study evaluates the efficacy and safety of obicetrapib as an adjunctive therapy in high-risk ASCVD patients.
Methods:
Online databases were searched. Outcomes included percentage changes in LDL-C, HDL-C, non-HDL-C, total cholesterol, triglyceride, ApoB, lipoprotein (a) [Lp(a)] and risk of any adverse events (AE), AE leading to discontinuation, acute kidney injury (AKI), transaminase or creatine kinase (CK) elevation and hypertension. Risk ratio (RR) for categorical outcomes and mean difference (MD) for continuous outcomes were reported using 95% confidence intervals (CI).
Results:
Three studies with 3088 patients (mean age 64 ± 11, 37% female) were selected. Obicetrapib significantly reduced LDL-C (-31.75%), non-HDL-C (-29.35%), triglyceride (-5.61%), Lp(a) (-35.67%), ApoB (-19.37%), and increased HDL-C (+125.94%) with no difference in total cholesterol levels. Obicetrapib was not associated with increased risk for any AE, AE leading to discontinuation, AKI, transaminase or CK elevation, and hypertension.
Conclusion:
Obicetrapib substantially improved lipid profiles in high-risk ASCVD patients on maximally tolerated lipid lowering therapy, without increased short-term adverse events. However, further long-term randomized studies are needed to confirm sustained efficacy, long-term safety, and potential impacts on clinical cardiovascular outcomes.
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