COMPARISON OF SERUM LIPOPROTEIN(A) DISTRIBUTION AND ITS CORRELATES AMONG BLACK-AND-WHITE POPULATIONS

Citation
P. Bovet et al., COMPARISON OF SERUM LIPOPROTEIN(A) DISTRIBUTION AND ITS CORRELATES AMONG BLACK-AND-WHITE POPULATIONS, International journal of epidemiology, 23(1), 1994, pp. 20-27
Citations number
39
Categorie Soggetti
Public, Environmental & Occupation Heath
ISSN journal
03005771
Volume
23
Issue
1
Year of publication
1994
Pages
20 - 27
Database
ISI
SICI code
0300-5771(1994)23:1<20:COSLDA>2.0.ZU;2-2
Abstract
Background Epidemiological data on serum lipoprotein(a) (Lp(a)), a pre sumably strong risk factor for coronary artery disease in White popula tions, has mostly been derived, in Black populations, from small sampl es. This study compares the distribution and the determinants of serum Lp(a) in Blacks and in Whites using large representative samples and the same methods in both populations. Methods The distribution and the correlates of serum Lp(a) were investigated in population-based sampl es of 701 Blacks in the Seychelles and 634 Whites in Switzerland, aged 25-64 years. Serum Lp(a) was quantified using a commercial immunoradi ometric assay. Results The distribution of serum Lp(a) was similarly s kewed in both ethnic groups, but median Lp(a) concentration was about twofold higher in Blacks (210 mg/l) compared to Whites (100 mg/l). The proportions of individuals with elevated serum Lp(a) (>300 mg/l) was about 50% higher in Blacks (37.5%) than in Whites (25.2%). In both eth nic groups, serum Lp(a) was found to correlate with total cholesterol, LDL-cholesterol and apoprotein B but not with HDL-cholesterol, alcoho l intake, smoking, and body mass index. The variance in serum Lp(a) co ncentration explained by any combination of these factors was smaller than 5.3% in the two populations. Conclusions The measured factors did not explain the higher levels of serum Lp(a) found in Blacks compared to Whites. These findings are consistent with the hypothesis that gen etic factors account for much of the variation of serum Lp(a) in both populations.