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Published on: October 12, 2017
The complexity of HDL
1Department of Medicine and UBC James Hogg Research Centre, Providence Heart and Lung Institute, 1081 Burrard St., Vancouver, British Columbia, Canada. gordon.fracis@hli.ubc.ca
Insights
High-density lipoprotein cholesterol (HDL-C) levels don't always predict heart disease risk. Research suggests HDL particle function, not just HDL-C levels, is key to its protective effects.
Area of Science:
- Cardiovascular Science
- Lipid Metabolism
- Biochemistry
Background:
- Plasma high-density lipoprotein cholesterol (HDL-C) is linked to reduced coronary artery disease (CAD) risk.
- However, HDL-C levels have exceptions in predicting individual patient outcomes.
- Emerging evidence points to HDL particle biology beyond HDL-C levels for in vivo effects.
Purpose of the Study:
- To review the protective role of HDL.
- To examine current HDL-based therapy evidence in humans and animals.
- To explore alternatives to HDL-C for assessing HDL function and clinical predictive value.
Main Methods:
- Literature review of epidemiological studies.
- Analysis of animal and human clinical trial data on HDL therapies.
- Examination of HDL particle formation, metabolism, and dysfunction.
Main Results:
- HDL-C levels have limitations in predicting CAD risk.
- HDL particle function appears more critical than HDL-C levels.
- Dysfunctional HDL is observed in diabetes and inflammatory conditions.
Conclusions:
- HDL's protective effects are complex and not fully captured by HDL-C.
- Assessing HDL function may offer better clinical prediction than HDL-C alone.
- Further research into HDL particle biology and function is warranted for therapeutic development.
Abstract:
Plasma high-density lipoprotein cholesterol (HDL-C) levels are inversely associated with coronary artery disease risk in large epidemiologic studies. This rule, however, has many exceptions in individual patients, and evidence suggests that other facets of high-density lipoprotein particle biology not captured by measuring HDL-C levels are responsible for HDL's effects in vivo. This article reviews the evidence for the protective nature of HDL, current evidence from animal and human studies regarding HDL-based therapies, the major steps in HDL particle formation and metabolism, alterations leading to dysfunctional HDL in diabetes and inflammatory states, and potential alternatives to HDL-C to measure HDL function and predict its protective value clinically.
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