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High-Density Lipoprotein Subpopulation Profile and Coronary Heart Disease Prevalence in Male Participants of the Framingham Offspring Study

298

Citations

28

References

2004

Year

TLDR

HDL is heterogeneous and the clinical relevance of its subspecies for coronary heart disease risk remains unclear. The study examined whether distinct HDL subpopulations are associated with coronary heart disease prevalence in men. ApoA‑I levels in HDL subfractions were quantified by native 2‑D gel electrophoresis, immunoblotting, and image analysis in male Framingham Offspring Study participants. Compared with controls, CHD cases had higher preβ‑1 and α‑3 and lower α‑1, preα‑3, and preα‑1 particles; α‑1 and preα‑3 were inversely, while α‑3 and preα‑1 were positively associated with CHD, with α‑1 HDL most strongly linked, reducing odds by 26% per mg/dL versus 2% for total HDL‑C.

Abstract

Objective— High-density lipoprotein (HDL) is a heterogeneous lipoprotein class and there is no consensus on the value of HDL subspecies in coronary heart disease (CHD) risk assessment. We tested the hypothesis whether specific HDL subpopulations are significantly associated with CHD-prevalence. Methods and Results— ApoA-I concentrations (mg/dL) in HDL subpopulations were quantitatively determined by native 2d gel electrophoresis, immunoblotting, and image analysis in male participants in the Framingham Offspring Study (FOS). CHD cases (n=169) had higher preβ-1 and α-3 particle and lower α-1, preα-3, and preα-1 particle levels than either all (n=1277) or HDL cholesterol-matched (n=358) controls. α-1 and preα-3 levels had an inverse association, whereas α-3 and preα-1 particle levels had a positive association with CHD prevalence after adjusting the data for established CHD risk factors. Standardized logit coefficients indicated that α-1 HDL was most significantly associated with CHD prevalence. Moreover, each mg/dL increase in α-1 particle level decreased odds of CHD by 26% ( P <0.0001), whereas each mg/dL increase in HDL cholesterol decreased odds of CHD by 2% in a model including all established CHD risk factors. Conclusions— Specific HDL subpopulations were positively correlated, whereas others were inversely correlated with CHD prevalence in male subject in the FOS, indicating that the various HDL particles might have different roles in the cause of CHD.

References

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