V. Giannelli, M. Simmaco, L. Lionetto, G. Gentile, M. Giusto, F. Ponziani, A. Gasbarrini, U. Visco-Comandini, A. Pellicelli, S. Corradini, A. Molinaro, E. Biliotti, M. Merli, G. Taliani
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引用次数: 0
摘要
平衡核苷转运蛋白1 (equilibrium Nucleoside Transporter 1, ENT1)的遗传多态性参与利巴韦林的细胞摄取,并能积极增强抗病毒治疗反应。肝移植环境为选择性观察供体肝脏ENT1基因对HCV治疗结果的影响提供了独特的机会。我们的目的是研究移植患者的供体ENT1多态性和HCV治疗结果。评价利巴韦林血药浓度的作用。纳入39例HCV复发患者。采用RNA PCR对供肝样本进行供体ENT1和IL-28B基因分型。肝脏ENT1等位基因频率为:AA 43.6%;AG) 28.2%;GG 28.2%。GG基因型与快速发病相关[RR=8;95% ci 1.6-38;p=0.01]和持续病毒学反应[RR=9.5;95% ci 1.6-53;p = 0.01)。在多因素分析中,GG基因型和12周时利巴韦林血药浓度>2.0 ng/mL与持续的病毒学反应独立相关。综上所述,耳鼻喉科基因多态性影响治疗反应,治疗前测定其活性有助于预测HCV患者的治疗反应。
Ribavirin Transporter [Ent1] Polymorphism is a Pretreatment Predictorof Virologic Response: The Specific Role of Donor Liver Transporter
The genetic polymorphism of Equilibrative Nucleoside Transporter 1 [ENT1] is involved in ribavirin cellular uptake and it could positively enhance antiviral treatment response. The liver transplant setting offers the unique opportunity to selectively observe the effect(s) of the donor liver ENT1 gene on HCV treatment outcome. We aimed at studying donor polymorphism of ENT1 and HCV therapy outcome in transplanted patients. The role of ribavirin plasma concentration was evaluated. 39 patients after HCV recurrence were included. Genotyping of donor ENT1 and of IL-28B was performed in donor liver samples by RNA PCR. Allelic frequencies of liver ENT1 were: AA 43.6%; AG 28.2%; GG 28.2%. GG genotype was associated with rapid [RR=8; 95% CI 1.6-38; p=0.01] and sustained virological response [RR=9.5; 95% CI 1.6-53; p=0.01]. In multivariate analysis, GG genotype and a ribavirin plasma concentration >2.0 ng/mL at week 12 were independently associated with sustained virological response. In conclusion, the genetic polymorphism of ENT influences treatment response and a pre-treatment determination of its activity could help to predict treatment response in HCV patients.