Interaction between SREBP-1a and APOB polymorphisms influences total and low-density lipoprotein cholesterol levels in patients with coronary artery disease

被引:17
作者
Rios, DLS
Vargas, AF
Torres, AMR
Zago, AJ
Callegari-Jacques, SM
Hutz, MH
机构
[1] Univ Fed Rio Grande do Sul, Inst Biociencias, Dept Genet, BR-91501970 Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Serv Cardiol, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Dept Estatist, Porto Alegre, RS, Brazil
关键词
APOB gene; apolipoproteins; genetic variability; haplotypes; lipid levels; SREBP-1a gene;
D O I
10.1034/j.1399-0004.2003.00057.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In this study, we examined the insertion/deletion (Ins/Del) and XbaI polymorphisms of the apolipoprotein B (APOB) gene and the -36delG polymorphism in the sterol regulatory element binding protein-1a (SREBP-1a) gene in 298 patients with non-diabetic angiographically assessed coronary artery disease (CAD), and 188 healthy controls, from a Brazilian population of European descent. Del/X+ haplotype carriers had higher levels of total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) in patients (TC, p = 0.05; LDL-C, p = 0.049) and controls (TC, p = 0.004; LDL-C, p = 0.013). No association was detected between the SREBP-1a -36delG polymorphism and lipid levels, but a significant interaction effect between APOB and SREBP-la polymorphisms was observed in the patient sample on TC (p = 0.005) and on LDL-C (p = 0.019) levels. Carriers of the APOB Del/X+ haplotype and SREBP-la G-G- genotype showed the highest levels of these lipid parameters. This effect of interaction was not observed in the control sample. Despite the associations with lipids, these polymorphisms were not associated with CAD risk or severity in this sample.
引用
收藏
页码:380 / 385
页数:6
相关论文
共 24 条
[1]   SUBGROUP STUDIES OF BLACK ADMIXTURE WITHIN A MIXED POPULATION OF BAHIA, BRAZIL [J].
AZEVEDO, ES .
ANNALS OF HUMAN GENETICS, 1980, 44 (JUL) :55-60
[2]   Apolipoprotein B signal peptide polymorphism in relation to lipids and diabetes in male CAD patients [J].
Benes, P ;
Muzik, J ;
Benedik, J ;
Elbl, L ;
Znojil, V ;
Vácha, J .
ATHEROSCLEROSIS, 2000, 152 (01) :257-258
[3]  
BOHN M, 1994, CLIN GENET, V45, P255
[4]   A proteolytic pathway that controls the cholesterol content of membranes, cells, and blood [J].
Brown, MS ;
Goldstein, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11041-11048
[5]  
Corbo RM, 1999, HUM BIOL, V71, P933
[6]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[7]   Association of the insertion/deletion gene polymorphism of the apolipoprotein B signal peptide with myocardial infarction [J].
Gardemann, A ;
Ohly, D ;
Fink, M ;
Katz, N ;
Tillmanns, H ;
Hehrlein, FW ;
Haberbosch, W .
ATHEROSCLEROSIS, 1998, 141 (01) :167-175
[9]  
HANSEN PS, 1994, CLIN GENET, V45, P78
[10]   Biosynthesis of apolipoprotein B48-containing lipoproteins - Regulation by novel post-transcriptional mechanisms [J].
Innerarity, TL ;
Boren, J ;
Yamanaka, S ;
Olofsson, SO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) :2353-2356