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Apolipoprotein A-I Infusions in Coronary Artery Disease: A Systematic Review
Rimsha Ahmad1, Syed Sadam Hussain1, Saifullah Khan2
1From the Department of Internal Medicine, Westchester Medical Center and New York Medical College, Valhalla, NY.
Insights
Apolipoprotein A-1 (apoA-1) infusions show promise for treating coronary artery disease (CAD) by improving HDL function and cholesterol clearance. This approach targets HDL functionality, not just cholesterol levels, for cardiovascular event reduction.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
- Pharmacology
Background:
- Coronary artery disease (CAD) remains a leading global cause of mortality.
- High-density lipoprotein (HDL) cholesterol-raising therapies have not consistently reduced cardiovascular events.
- Focus is shifting towards HDL functionality, specifically cholesterol efflux capacity (CEC).
Purpose of the Study:
- To review the rationale for using apolipoprotein A-1 (apoA-1) infusions.
- To summarize the clinical trial landscape for apoA-1 infusions in CAD.
- To explore apoA-1 as a novel therapeutic target for CAD.
Main Methods:
- Review of preclinical studies on apoA-1's antiatherogenic effects.
- Analysis of early-phase human trials involving apoA-1 infusions.
- Examination of apoA-1's role in reverse cholesterol transport and CEC.
Main Results:
- ApoA-1 infusions demonstrated antiatherogenic effects in preclinical models.
- Early human trials suggest apoA-1 infusions enhance CEC and cholesterol clearance.
- ApoA-1 infusions may offer a new strategy beyond raising HDL-C levels.
Conclusions:
- ApoA-1 infusions represent a promising therapeutic strategy for CAD.
- Targeting HDL functionality via apoA-1 is a key area for cardiovascular research.
- Further clinical trials are evaluating apoA-1 infusions for CAD prevention and treatment.
Abstract:
Coronary artery disease (CAD) is the leading cause of death globally. Apolipoprotein A-1 (apoA-1), the primary protein component of high-density lipoprotein (HDL), facilitates reverse cholesterol transport and has emerged as a potential therapeutic target. While pharmacologic efforts to raise HDL-C levels have failed to reduce cardiovascular events, focus has shifted to HDL functionality, particularly cholesterol efflux capacity (CEC). ApoA-1 infusions have demonstrated antiatherogenic effects in preclinical models and early human trials by enhancing CEC and promoting cholesterol clearance. This review summarizes the rationale and evolving clinical trial landscape investigating apoA-1 infusions as a novel therapy for CAD prevention and treatment.
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