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Updated: May 1, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Current guidelines for high-density lipoprotein cholesterol in therapy and future directions
Bishnu H Subedi1, Parag H Joshi2, Steven R Jones2
1Johns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, MD, USA ; Greater Baltimore Medical Center, Baltimore, MD, USA.
Insights
Low high-density lipoprotein cholesterol (HDL-C) is a risk factor for atherosclerotic cardiovascular disease (ASCVD). While increasing HDL-C was a therapeutic goal, recent trials challenge this, necessitating new strategies for HDL therapeutics.
Area of Science:
- Cardiology
- Biochemistry
- Pharmacology
Background:
- Low high-density lipoprotein cholesterol (HDL-C) is a significant risk factor for atherosclerotic cardiovascular disease (ASCVD).
- Therapeutic strategies aimed at increasing HDL-C levels have been pursued, with some agents showing modest HDL-C increases and ASCVD event reduction in the past.
- Recent clinical trials have questioned the direct correlation between elevated HDL-C levels and cardiovascular benefits, leading to controversy surrounding the HDL hypothesis.
Purpose of the Study:
- To review current therapeutic approaches targeting HDL-C for ASCVD.
- To explore emerging and novel strategies for HDL therapeutics that focus on HDL's structure and function.
- To discuss future directions in the development of agents that mimic or enhance HDL's cardioprotective properties.
Main Methods:
- Literature review of clinical trials and therapeutic strategies related to HDL-C.
- Analysis of findings from randomized trials involving niacin and cholesteryl ester transfer protein inhibitors.
- Discussion of novel therapeutic approaches in early-phase development.
Main Results:
- Past therapies like fibrates and niacin showed modest HDL-C increases and some ASCVD event reduction.
- Recent randomized trials have challenged the assumption that higher HDL-C levels uniformly lead to ASCVD benefits.
- Current guidelines lack clear direction for targeting HDL-C due to insufficient outcome data for HDL-specific therapies.
Conclusions:
- The direct benefit of quantitatively increasing HDL-C for ASCVD prevention is now debated.
- Novel therapeutic strategies are being developed to mimic HDL structure or enhance its functions beyond cholesterol transport.
- Future HDL therapeutics may involve approaches like HDL infusions, Apo A-I mimetics, and gene therapy, pending early-phase trial results.
Abstract:
Many studies have suggested that a significant risk factor for atherosclerotic cardiovascular disease (ASCVD) is low high-density lipoprotein cholesterol (HDL-C). Therefore, increasing HDL-C with therapeutic agents has been considered an attractive strategy. In the prestatin era, fibrates and niacin monotherapy, which cause modest increases in HDL-C, reduced ASCVD events. Since their introduction, statins have become the cornerstone of lipoprotein therapy, the benefits of which are primarily attributed to decrease in low-density lipoprotein cholesterol. Findings from several randomized trials involving niacin or cholesteryl ester transfer protein inhibitors have challenged the concept that a quantitative elevation of plasma HDL-C will uniformly translate into ASCVD benefits. Consequently, the HDL, or more correctly, HDL-C hypothesis has become more controversial. There are no clear guidelines thus far for targeting HDL-C or HDL due to lack of solid outcomes data for HDL specific therapies. HDL-C levels are only one marker of HDL out of its several structural or functional properties. Novel approaches are ongoing in developing and assessing agents that closely mimic the structure of natural HDL or replicate its various functions, for example, reverse cholesterol transport, vasodilation, anti-inflammation, or inhibition of platelet aggregation. Potential new approaches like HDL infusions, delipidated HDL, liver X receptor agonists, Apo A-I upregulators, Apo A mimetics, and gene therapy are in early phase trials. This review will outline current therapies and describe future directions for HDL therapeutics.
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