Platelet collagen receptor GPla (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men

被引:8
作者
Mikkelsson, J
Perola, M
Penttilä, A
Karhunen, PJ
机构
[1] Univ Tampere, FIN-33014 Tampere, Finland
[2] Tampere Univ Hosp, FIN-33014 Tampere, Finland
[3] Univ Helsinki, Dept Forens Med, Helsinki, Finland
[4] Univ Kuopio, Dept Clin Pathol & Forens Med, FIN-70211 Kuopio, Finland
[5] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
[6] Univ Calif Los Angeles, Dept Human Genet, Gonda Neurosci & Genet Res Ctr, Los Angeles, CA USA
关键词
coronary thrombosis; glycoprotein GPIa/IIa; myocardial infarction; polymorphism; genetics;
D O I
10.1016/S0021-9150(02)00110-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelet CPIa/IIa receptors play key roles in the adhesion of platelets to collagen during the formation of coronary thrombosis. The C807T and HPA-5 polymorphisms of the gene for GPIa define three distinct alleles of GPIa which are associated with the surface expression of the protein in an allele-dependent fashion. Significance of these polymorphisms in victims of sudden cardiac death (SCD) was studied in Helsinki Sudden Death Study (HSDS) comprising 700 autopsied middle-aged Caucasian Finnish men with 288 SCD victims and 84 men with fatal acute myocardial infarction (AMI). The high-expression A1 allele was found in 36.6% of control men as opposed to 38.0% of all SCD victims and 36.9% of men with fatal AMI (P > 0.4). The high-expression A1A1 genotype was found in 11.9% of men with fatal AMI and 10.0% of controls as opposed to the low-expression A2A2 genotype which was found in 29.8% of men with fatal AMI and in 31.2% of controls (OR 1.2, P > 0.3). Age group (under/over 55) had no effect on the results. Our results do not support an effect of the GPIa haplotype on fatal coronary events among middle-aged men. ( D 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 118
页数:8
相关论文
共 51 条
[51]   RISK-FACTORS FOR SUDDEN CARDIAC DEATH IN MIDDLE-AGED BRITISH MEN [J].
WANNAMETHEE, G ;
SHAPER, AG ;
MACFARLANE, PW ;
WALKER, M .
CIRCULATION, 1995, 91 (06) :1749-1756