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.