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首页> 外文期刊>Liver international : >Contribution of ribavirin transporter gene polymorphism to treatment response in peginterferon plus ribavirin therapy for HCV genotype 1b patients
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Contribution of ribavirin transporter gene polymorphism to treatment response in peginterferon plus ribavirin therapy for HCV genotype 1b patients

机译:利巴韦林转运蛋白基因多态性对聚乙二醇干扰素加利巴韦林治疗HCV基因型1b患者的治疗反应的贡献

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Background: Standard-dose ribavirin is crucial for the standard-of-care treatment of chronic hepatitis C virus (HCV) infection. Equilibrative nucleoside transporter 1 (ENT1), encoded by SLC29A1 gene, is the main transporter that imports ribavirin into human hepatocytes. Aims: To determine whether single nucleotide polymorphisms (SNPs) at the SLC29A1 gene could influence the probability of treatment response compared with other baseline and host genetic factors. Methods: A total of 526 East Asian patients monoinfected with HCV genotype 1b who had received pegylated interferon alpha plus ribavirin therapy were enrolled in this study. They were assigned randomly to the derivation and confirmatory groups. SNPs related to the IL28B, ITPA and SLC29A1 genes were genotyped using real-time detection polymerase chain reaction. Factors associated with sustained virological response (SVR) were analysed using multiple logistic regression analysis. Results: Multivariate analysis for the derivation group identified six baseline variables significantly and independently associated with SVR: age [P = 0.023, odds ratio (OR) = 0.97], gender (P = 0.0047, OR = 2.25), platelet count (P = 0.00017, OR = 1.11), viral load (P = 0.00026, OR = 0.54), IL28B SNP rs12979860 (P = 1.09 × 10 -7, OR = 8.68) and SLC29A1 SNP rs6932345 (P = 0.030, OR = 1.85). Using the model constructed by these independent variables, positive and negative predictive values and predictive accuracy were 73.3, 70.1 and 71.9% respectively. For the confirmatory group, they were 71.4, 84.6 and 75.3% respectively. The SLC29A1 and IL28B SNPs were also significantly associated with rapid virological response. Conclusions: The SNP at the major ribavirin transporter ENT1 gene SLC29A1 was one of significantly independent factors influencing treatment response, although the impact on the prediction was small.
机译:背景:标准剂量的利巴韦林对于慢性丙型肝炎病毒(HCV)感染的标准治疗至关重要。由SLC29A1基因编码的平衡核苷转运蛋白1(ENT1)是将利巴韦林导入人肝细胞的主要转运蛋白。目的:确定与其他基线和宿主遗传因素相比,SLC29A1基因上的单核苷酸多态性(SNP)是否会影响治疗反应的可能性。方法:本研究共纳入了526名接受聚乙二醇干扰素α加利巴韦林治疗的HCV基因型1b单感染的东亚患者。他们被随机分配到派生和确认组。使用实时检测聚合酶链反应对与IL28B,ITPA和SLC29A1基因相关的SNP进行基因分型。使用多重逻辑回归分析对与持续病毒学应答(SVR)相关的因素进行了分析。结果:衍生组的多变量分析确定了六个与SVR显着且独立相关的基线变量:年龄[P = 0.023,优势比(OR)= 0.97],性别(P = 0.0047,OR = 2.25),血小板计数(P = 0.00017,OR = 1.11),病毒载量(P = 0.00026,OR = 0.54),IL28B SNP rs12979860(P = 1.09×10 -7,OR = 8.68)和SLC29A1 SNP rs6932345(P = 0.030,OR = 1.85)。使用由这些独立变量构建的模型,阳性和阴性预测值和预测准确性分别为73.3%,70.1和71.9%。确认组分别为71.4%,84.6%和75.3%。 SLC29A1和IL28B SNP也与快速病毒学应答显着相关。结论:主要病毒唑转运蛋白ENT1基因SLC29A1上的SNP是影响治疗反应的显着独立因素之一,尽管对预测的影响很小。

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