The GPIa C807T dimorphism associated with platelet collagen receptor density is not a risk factor for myocardial infarction

The platelet collagen receptor. GPIa/IIa, is an important mediator of plate let adhesion to fibrillar collagens at sites of vascular injury Recently, a dimorphism at nucleotide 807 of the GPIa cDNA (TTC/TTT in codon 224) was s hown to be associated with variation in GPIa/IIa receptor density on the pl atelet surface. We conducted a case-control study to determine if the 807T allele, linked with increased GPIa/IIa density, contributed to risk of myoc ardial infarction (MI). DNA from 546 acute MI cases and 507 controls, all a ged <75 years. was genotyped for the C807T dimorphism using the TaqMan(TM) system of allelic discrimination. The allelic odds ratio (OR) for MI in the complete cohort was 0.88 (95% CI 0.74-1.05, P=0.17), indicating that the 8 07T allele was not associated with an increased risk of MI. There was also no increased risk of MI associated with the homozygous 807TT (P=0.22) or he terozygous 807CT (P=0.24) genotypes or for carriers of the 807T allele in a ny cohort subgroup analysed. We conclude that the GPIa 807T allele is not a risk factor for MI in our population either alone or in combination with o ther major cardiovascular risk factors.