Hospital General de Zona 24, Instituto Mexicano Del Seguro Social, Mexico, DF, Mexico.
Mol Cell Biochem. 2013 Dec;384(1-2):163-71. doi: 10.1007/s11010-013-1794-4. Epub 2013 Sep 5.
It has been identified that platelet glycoprotein IIIa PIA1/A2 polymorphism plays an important role in atherothrombotic disease such as myocardial infarction and stroke, but results remain controversial. Here, we investigated whether the PIA2 allele is associated with ST myocardial infarction or idiopathic ischemic stroke in young individuals in two independent studies. In a case-control study 275 patients with ST elevation myocardial infarction ≤45 years of age and 278 controls were recruited. In a second study, 200 patients with idiopathic ischemic stroke ≤45 years of age and 200 controls were enrolled. In both studies cases and controls were matched by age and gender. The PIA1/A2 polymorphism was determined in all participants by a polymerase chain reaction-restriction fragment length polymorphism assay. There was a significant difference in the PIA1/A2 genotype distribution (P = 0.001) and allele frequency (P = 0.001), between ST elevation myocardial infarction and control groups, but not in the PIA1/A2 genotype distribution (P = 0.61) and allele frequency (P = 0.80), between idiopathic ischemic stroke. The allele PIA2 represented an independent risk for ST elevation myocardial infarction but not for idiopathic ischemic stroke. Hypertension, smoking, and family history of atherothrombotic disease were also associated with ST elevation myocardial infarction and idiopathic ischemic stroke. Our results suggest that PA2 allele represents a risk factor for ST elevation myocardial infarction in young Mexican individuals but not for idiopathic ischemic stroke.
已经确定血小板糖蛋白 IIIa PIA1/A2 多态性在动脉粥样硬化性疾病(如心肌梗死和中风)中起着重要作用,但结果仍存在争议。在这里,我们在两项独立的研究中研究了 PIA2 等位基因是否与年轻个体的 ST 段抬高型心肌梗死或特发性缺血性卒中有关。在病例对照研究中,纳入了 275 例年龄≤45 岁的 ST 段抬高型心肌梗死患者和 278 例对照者。在第二项研究中,纳入了 200 例年龄≤45 岁的特发性缺血性卒中患者和 200 例对照者。在两项研究中,病例和对照者均按年龄和性别匹配。所有参与者的 PIA1/A2 多态性均通过聚合酶链反应-限制性片段长度多态性分析确定。ST 段抬高型心肌梗死组和对照组之间 PIA1/A2 基因型分布(P=0.001)和等位基因频率(P=0.001)存在显著差异,但在特发性缺血性卒中组中 PIA1/A2 基因型分布(P=0.61)和等位基因频率(P=0.80)无显著差异。PIA2 等位基因代表 ST 段抬高型心肌梗死的独立危险因素,但不是特发性缺血性卒中的危险因素。高血压、吸烟和动脉粥样硬化性疾病的家族史也与 ST 段抬高型心肌梗死和特发性缺血性卒中有关。我们的结果表明,PA2 等位基因代表了年轻墨西哥个体 ST 段抬高型心肌梗死的危险因素,但不是特发性缺血性卒中的危险因素。