Concentrations of high-density lipoprotein subfraction HDL2 and lipoprotein A-I in a random population of healthy subjects

Author:

Roche D1,Migueres M L1,Lequang N T1,Burstein M2,Ekindjian O G1,Girard-Globa A34

Affiliation:

1. Laboratoire Central de Biochimie, Hôpital Laënnec, 42 rue de Sévres, 75007 Paris, France

2. Centre National de la Transfusion Sanguine, Paris

3. INSERM, U 286, Faculté de Médecine X Bichat, Paris

4. Nonstandard abbreviations: HDL, LDL, VLDL, high-, low-, and very-low-density lipoproteins, respectively; apo, apolipoprotein; Lp, lipoprotein; LpA-I:A-II, apoA-I associated with apoA-II in lipoparticles; and ANOVA, analysis of variance

Abstract

Abstract High-density lipoproteins (HDL) are now currently subdivided according either to density and size—HDL2 and HDL3—or to surface apoprotein composition—lipoprotein A-I (LpA-I) without A-II, and LpA-I:A-II. In samples from blood bank donors (60 women, 47 men), we evaluated HDL subclasses, LpA-I particles, and other classic risk factors for atherosclerosis and compared them with each other. We found a good correlation between HDL2 and LpA-I (r = 0.74, P < 0.001), the correlation being more marked in women (r = 0.74) than in men (r = 0.67). LpA-I was also strongly correlated with total apolipoprotein A-I (apoA-I) (r = 0.61), which suggests that LpA-I represents a significant portion of the variable pool of apoA-I. By contrast, LpA-I:A-II but not LpA-I was correlated with HDL3, confirming the preferential association of LpA-I with HDL2. The difference between the sexes was more marked for HDL2 (+66% in women) than for LpA-I (+25%). We conclude that in normolipemic subjects the size of the HDL2 pool depends on that of LpA-I. Considering the speed and low cost of the assay, determination of HDL2 cholesterol might be a useful tool for assessing cardiovascular risk.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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