Gender related association between genetic variations of APOC-III gene andlipid and lipoprotein variables in northern France

Citation
J. Dallongeville et al., Gender related association between genetic variations of APOC-III gene andlipid and lipoprotein variables in northern France, ATHEROSCLER, 150(1), 2000, pp. 149-157
Citations number
36
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
ATHEROSCLEROSIS
ISSN journal
00219150 → ACNP
Volume
150
Issue
1
Year of publication
2000
Pages
149 - 157
Database
ISI
SICI code
0021-9150(200005)150:1<149:GRABGV>2.0.ZU;2-3
Abstract
The goal of the present study was to assess the impact of variability at th e APOC-III insulin response element (APOC-III IRE) genetic locus on lipid, lipoprotein and complex lipoprotein particle levels as well as on the risk of dyslipidemia, in the population of northern France. To this end, 590 men and 579 women were randomly selected in the urban community of Lille in th e framework of the MONICA project. Three polymorphisms, - 482, - 455 in the APOC-III insulin response element (IRE) and SstI in the 3'-noncoding regio n of the APOC-III gene locus were assessed. Compared to the most common all eles, the rare alleles of -482 and -455 were associated with increased leve ls of apoB-containing particles (LDL-cholesterol, apoB) and of triglyceride -related markers (apoC-III and LpC-III:B) in women, but not in men, suggest ing a gender-related impact of APOC-III polymorphisms on these variables. S imilarly, triglycerides, LpC-III:B and apoB were higher in women bearing th e rare allele of SstI than in those with the most common allele. There was no evidence for any significant association between any of the - 482, - 455 , and SstI alleles and lipid disorders (mixed hyperlipidemia, hypertriglyce ridemia and hypercholesterolemia) in this sample of randomly selected men a nd women from northern France. In contrast, the prevalence of the haplotype that combined the rare alleles of the - 482 and -455 sites was increased o nly in women with hypertriglyceridemia. Therefore, although the individual risk of hypertriglyceridemia is increased in women with the haplotype T, C at -482, -455, it appears that the -482, -455 and SstI APOC-III gene polymo rphisms are not major contributors to the risk of dyslipidemia in the popul ation of northern France. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.