Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad-500016, India.
J Neurol Sci. 2012 Apr 15;315(1-2):72-6. doi: 10.1016/j.jns.2011.11.027. Epub 2011 Dec 15.
Aspirin is the most commonly used antiplatelet drug for treatment of a serious vascular event, most notably myocardial infarction and stroke. Significant fraction of aspirin treated patients is resistant to the antiplatelet effects of the drugs. Previous studies have suggested that a genetic basis for aspirin resistance exists. Therefore the present study was taken up to investigate the role of C3435T polymorphism (rs 1045642) of multiple drug resistance-1 (MDR-1) gene with aspirin resistance in stroke patients. Five hundred and sixty ischemic stroke patients and 560 age and sex matched healthy controls were involved in the study. Baseline clinical data were collected and follow-up telephone interviews were conducted with patients at 3, 6 and 12 months post event to determine stroke outcome. Blood samples were collected and genotypes determined. Significant difference was observed in the genotype distribution and allele frequency between patients and controls. The results were confirmed by a step wise multiple logistic regression analysis controlling all other confounding risk factors [adjusted Odds ratio=3.132 (95% CI; 2.043-4.800; p<0.001)]. There was a significant difference in genotype distribution between drug responders and non-responders. The risk of aspirin resistance was significantly high in patients with TT genotype in comparison to those with CC genotype [(TT vs. CC, χ(2)=6.268; p=0.012, Odds ratio=1.85) (95% CI; 1.142-3.017) (adjusted Odds ratio=2.465; 95% CI; 1.895-4.625 and p<0.001)]. As far as the stroke subtypes are concerned TT genotype associated significantly with aspirin resistance in intracranial large artery atherosclerosis. Our results indicate that the risk of aspirin resistance is more in patients with 3435TT genotype than in those with CC genotype. However, this is a preliminary study and a large study of replication is needed to confirm our results.
阿司匹林是治疗严重血管事件(尤其是心肌梗死和中风)最常用的抗血小板药物。在接受阿司匹林治疗的患者中,有相当一部分人对药物的抗血小板作用产生抵抗。先前的研究表明,阿司匹林抵抗存在遗传基础。因此,本研究旨在探讨多药耐药-1(MDR-1)基因 C3435T 多态性(rs1045642)与中风患者阿司匹林抵抗之间的关系。本研究纳入了 560 例缺血性中风患者和 560 名年龄和性别匹配的健康对照者。收集基线临床数据,并在事件发生后 3、6 和 12 个月对患者进行电话随访,以确定中风结局。采集血样并确定基因型。患者和对照组之间的基因型分布和等位基因频率存在显著差异。通过逐步多元逻辑回归分析控制所有其他混杂风险因素后,结果得到了证实[调整后的优势比=3.132(95%置信区间;2.043-4.800;p<0.001)]。药物反应者和非反应者之间的基因型分布存在显著差异。与 CC 基因型相比,TT 基因型患者发生阿司匹林抵抗的风险显著升高[(TT 与 CC,χ(2)=6.268;p=0.012,优势比=1.85)(95%置信区间;1.142-3.017)(调整后的优势比=2.465;95%置信区间;1.895-4.625,p<0.001)]。就中风亚型而言,TT 基因型与颅内大动脉粥样硬化性阿司匹林抵抗显著相关。我们的研究结果表明,3435TT 基因型患者发生阿司匹林抵抗的风险高于 CC 基因型患者。然而,这只是一项初步研究,需要进行大规模的复制研究来证实我们的结果。