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OPN Gene Polymorphism and the Serum OPN Levels Confer the Susceptibility and Prognosis of Ischemic Stroke in Chinese Patients

机译:OPN基因多态性和血清OPN水平赋予中国患者缺血性中风的易感性和预后

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biAim /i/bTo investigate the association of Osteopontin (OPN) gene polymorphism and serum thrombin-cleaved OPN level with the susceptibility to ischemic stroke (IS) and its prognosis. biMethods /i/bA total of 377 patients with IS and 551 healthy individuals were recruited. The OPN gene polymorphisms at -156 GGG, -443 CT and -66 TG were genotyped. Serum full-length and the thrombin-cleaved OPN were determined. biResults /i/bWe found that only the -443 CT polymorphism was significantly associated with the susceptibility to IS. The -443 CC represented a near 2 time higher risk for IS incidence than TT carriers. Also, the -443 CC genotype had significantly poorer outcome and they significantly had higher occurrence for bad recovery as determined by modified Rankin Scale (mRS) (OR=2.18, p=0.043) and Barthel Index (BI) (OR=2.12, p=0.05). The mean serum thrombin-cleaved OPN level in IS group were significantly higher than that in control group. ROC analysis showed that the thrombin-cleaved OPN level (cut-off value, 166.8 ng/ml) can discriminate IS patients from controls with a specificity of 86.3% and a sensitivity of 57.7%. The serum thrombin-cleaved OPN was significantly associated with the clinical outcome at 12 months after discharge from hospital. biConclusion /i/bThese results suggest that the -443 CT polymorphism of OPN gene and serum thrombin-cleaved OPN can be used as a biomarker for the susceptibility and prognosis of IS patients.
机译:目标 研究骨桥蛋白(OPN)基因多态性和血清凝血酶裂解的OPN水平与缺血性卒中(IS)的易感性及其预后的关系。 方法 总共招募了377名IS患者和551名健康个体。对-156 G> GG,-443 C> T和-66 T> G的OPN基因多态性进行基因分型。测定血清全长和凝血酶切割的OPN。 结果 我们发现,只有-443 C> T多态性与IS的易感性显着相关。 -443 CC代表IS发生风险比TT携带者高近2倍。而且,-443 CC基因型的结局明显较差,并且通过改良的兰金评分(mRS)(OR = 2.18,p = 0.043)和Barthel Index(BI)(OR = 2.12,p = 0.05)。 IS组的平均血清凝血酶裂解OPN水平显着高于对照组。 ROC分析显示,凝血酶裂解的OPN水平(临界值166.8 ng / ml)可以将IS患者与对照组区分,特异性为86.3%,敏感性为57.7%。出院后12个月,血清凝血酶裂解的OPN与临床结局显着相关。 结论 这些结果表明,OPN基因的-443 C> T多态性和血清凝血酶裂解的OPN可以作为IS患者易感性和预后的生物标志物。

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