Wibowo Samekto, Haryana Sofia Mubarika, Astuti Indwiani, Nurwidya Fariz
Department of Neurology, Faculty of Medicine, Universitas Syiah Kuala, Banda Aceh, Indonesia.
Department of Neurology, Faculty of Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia.
BMC Res Notes. 2018 Oct 11;11(1):718. doi: 10.1186/s13104-018-3823-6.
The identification of new genetic-associated risk factor of ischemic stroke could improves strategies for stroke prevention. This study aims to identify insulin receptor substrate 1 (IRS-1) gene polymorphism Gly972Arg as the risk factor for ischemic stroke among Indonesian subjects. The case-control study was conducted by matching the gender and race on 85 cases of patients with ischemic stroke and 86 healthy non-stroke control subjects. Ischemic stroke was established by the complete neurology examination and brain computed tomography scan or magnetic resonance imaging. Polymerase chain reaction-Restriction Fragment Length Polymorphism was performed to analyze IRS-1 gene Gly972Arg genotype.
There were 85 ischemic stroke cases and 86 control subjects. The distribution of nucleotide IRS-1 gene polymorphism Gly972Arg in the ischemic stroke vs health controls for GG were 32.2% vs 41.5%, for GR were 16% vs 7.6%, and for RR were 0.5% vs 1.9%. IRS-1 gene polymorphism Gly972Arg was found as significant risk factor for ischemic stroke [odds ratio of 2.6 (1.27-5.27); CI 95%, p = 0.008]. Conclusively, the IRS-1 gene polymorphism Gly972Arg should be considered as an important factor in the prevention and treatment of ischemic stroke.
识别缺血性中风新的基因相关危险因素有助于改进中风预防策略。本研究旨在确定胰岛素受体底物1(IRS-1)基因多态性Gly972Arg是印度尼西亚受试者缺血性中风的危险因素。通过匹配性别和种族,对85例缺血性中风患者和86例健康非中风对照者进行了病例对照研究。通过全面的神经学检查以及脑部计算机断层扫描或磁共振成像确诊缺血性中风。采用聚合酶链反应-限制性片段长度多态性方法分析IRS-1基因Gly972Arg基因型。
共有85例缺血性中风病例和86例对照者。在缺血性中风组与健康对照组中,IRS-1基因多态性Gly972Arg的核苷酸分布情况为:GG型分别为32.2%和41.5%,GR型分别为16%和7.6%,RR型分别为0.5%和1.9%。发现IRS-1基因多态性Gly972Arg是缺血性中风的显著危险因素[比值比为2.6(1.27 - 5.27);95%置信区间,p = 0.008]。总之,IRS-1基因多态性Gly972Arg应被视为缺血性中风预防和治疗中的一个重要因素。