Association between platelet glycoprotein Ib alpha genotype and ischemic cerebrovascular disease

Citation
A. Sonoda et al., Association between platelet glycoprotein Ib alpha genotype and ischemic cerebrovascular disease, STROKE, 31(2), 2000, pp. 493-497
Citations number
35
Categorie Soggetti
Neurology,"Cardiovascular & Hematology Research
Journal title
STROKE
ISSN journal
00392499 → ACNP
Volume
31
Issue
2
Year of publication
2000
Pages
493 - 497
Database
ISI
SICI code
0039-2499(200002)31:2<493:ABPGIA>2.0.ZU;2-U
Abstract
Background and Purpose-Platelets play pivotal roles in the development of i schemic cerebrovascular disease (CVD), The platelet glycoprotein (GP) Ib/IX /V complex is a receptor for von Willebrand factor, which plays a major rol e in the initial phase of platelet activation under high shear stress condi tions. This study was designed to investigate the association between a gen etic variation of this receptor and the prevalence of CVD, Methods-Two hundred patients with ischemic CVD, as confirmed by brain CT an d/or MRI, and 317 age- and sex-matched control subjects without clinical ev idence of CVD or cardiovascular disease were analyzed for their genotype fr equencies of the (145)Thr/Met dimorphism of the a-chain of GPIb (GPIb alpha ), Results-Genotypes with (145)Met (T/M and M/M) were more frequently found in the CVD patients (26.5%) than in control subjects (14.2%, P=0.0005). The g enotype effect was more obvious in those <60 years of age or without acquir ed cardiovascular risk factors. The odds ratio for nonsmoking women <60 yea rs of age was 10.6 (95% confidence intervals, 2.2 to 51.7). Although the nu mber of patients studied was small (n=24), transient ischemic attack showed the highest odds ratio (4.3, P=0.0004), followed by lacunar infarction (OR =2.2, P=0.0024) and atherothrombotic infarction (OR= 1.5, P=0.3143), Logist ic regression analysis revealed that the presence of Met-allele was indepen dently associated with CVD, Conclusions-Our study suggests that the platelet GPIba genotype is a geneti c risk factor for ischemic CVD.