Why the study?
Is HDL-3 a better predictor of carotid artery disease than HDL-2, HDL-C, or apolipoprotein A1?
Is HDL-3 a better predictor of carotid artery disease than HDL-2, HDL-C, or apolipoprotein A1?
HDL-3 levels are a superior predictor of carotid artery disease compared to HDL-2, total HDL-C, or apolipoprotein A1, suggesting a specific atheroprotective role for this subfraction.
Answers are grounded in this paper and cite their sources.
HDL-3 may refine carotid atherosclerosis risk stratification beyond standard HDL measures; observational data leave open clinical utility pending prospective validation.
BACKGROUND: Recent data suggest that high-density lipoprotein cholesterol (HDL-C) levels are likely not in the causative pathway of atheroprotection, shifting focus from HDL-C to its subfractions and associated proteins. This study's goal was to determine which HDL phenotype was the better predictor of carotid artery disease (CAAD). METHODS AND RESULTS: HDL-2 and HDL-3 were measured in 1725 participants of European ancestry in a prevalent case-control cohort study of CAAD. Stratified analyses were conducted for men (n=1201) and women (n=524). Stepwise linear regression was used to determine whether HDL-C, HDL-2, HDL-3, or apolipoprotein A1 was the best predictor of CAAD, while adjusting for the confounders of censored age, diabetes, and current smoking status. In both men and women, HDL-3 was negatively associated with CAAD (P=0.0011 and 0.033 for men and women, respectively); once HDL-3 was included in the model, no other HDL phenotype was significantly associated with CAAD. Addition of paraoxonase 1 activity to the aforementioned regression model showed a significant and independent (of HDL-3) association with CAAD in men (P=0.001) but not in the smaller female subgroup. CONCLUSIONS: This study is the first to contrast the associations of HDL-2 and HDL-3 with CAAD. We found that HDL-3 levels were more predictive of CAAD status than HDL-2, HDL-C, or apolipoprotein A1. In addition, for men, paraoxonase 1 activity improved the overall model prediction for CAAD independently and additively with HDL-3 levels. Further investigation into the molecular mechanisms through which HDL-3 is associated with protection from CAAD is warranted.
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Kim et al. (2014) studied this question.
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