首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Interferon lambda 3 rs12979860 polymorphism in patients with haemophilia and HCV infection: A predictor of spontaneous viral clearance and sustained virological response
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Interferon lambda 3 rs12979860 polymorphism in patients with haemophilia and HCV infection: A predictor of spontaneous viral clearance and sustained virological response

机译:血友病和HCV感染患者的干扰素λ3 rs12979860基因多态性:自发病毒清除和持续病毒学应答的预测因子

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Chronic hepatitis C is the main cause of morbidity and mortality in adult haemophilic patients who received non-virally inactivated plasma- derived clotting factor concentrates. Overall, spontaneous viral clearance rate is 10-25% and the only approach that can halt disease progression is hepatitis C virus (HCV) eradication by means of antiviral therapy. In non-haemophilic patients a single nucleotide polymorphism located upstream the gene of interferon lambda 3 (IFN3) has been associated with both spontaneous viral clearance and sustained virological response after antiviral treatment. The aim of this study was to assess whether the rs12979860 polymorphism was a predictor of spontaneous viral clearance and of sustained virological response after antiviral therapy in a large cohort of haemophilic patients with HCV infection. The rs12979860 polymorphism, defined as CC genotype or T allele, was tested in a cohort of 342 haemophilic patients and evaluated as predictor of spontaneous clearance or response to antiviral therapy. By multivariate regression analysis the IFN3 CC genotype was an independent predictor of spontaneous viral clearance (odds ratio: 3.7, 95% confidence interval: 2.0-6.8). Sustained virological response rates were doubled in patients with the CC genotype than in those with the T allele (78% vs 44%; p<0.001), especially in patients with HCV type 1 (67% vs 32%; p<0.001) and higher sustained response rates were observed in patients with the CC genotype who did not achieve rapid virological response (61% vs 30% in T allele patients; p=0.006).
机译:慢性丙型肝炎是接受非病毒灭活的血浆来源的凝血因子浓缩物的成年血友病患者发病和死亡的主要原因。总体而言,自发病毒清除率为10%至25%,并且唯一可以阻止疾病进展的方法是通过抗病毒疗法根除丙型肝炎病毒(HCV)。在非血友病患者中,位于干扰素λ3(IFN3)基因上游的单核苷酸多态性与自发病毒清除和抗病毒治疗后持续的病毒学应答有关。这项研究的目的是评估rs12979860基因多态性是否可预测大量人群HCV感染的血友病患者抗病毒治疗后病毒自发清除和持续病毒学应答。 rs12979860多态性(定义为CC基因型或T等位基因)在342名血友病患者队列中进行了测试,并被评估为自发清除或对抗病毒治疗的反应的预测因子。通过多元回归分析,IFN3 CC基因型是自发病毒清除率的独立预测因子(几率:3.7,95%置信区间:2.0-6.8)。 CC基因型患者的持续病毒学应答率是T等位基因患者的两倍(78%vs 44%; p <0.001),尤其是1型HCV患者(67%vs 32%; p <0.001)和在没有快速病毒学应答的CC基因型患者中观察到更高的持续应答率(T等位基因患者为61%vs 30%; p = 0.006)。

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