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Roles of ITPA and IL28B Genotypes in Chronic Hepatitis C Patients Treated with Peginterferon Plus Ribavirin

机译:聚乙二醇干扰素联合利巴韦林治疗慢性丙型肝炎患者中ITPA和IL28B基因型的作用

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摘要

It has been reported that inosine triphosphatase (ITPA) gene variants protect against ribavirin-induced anemia in patients treated for chronic hepatitis C. IL28B variants also influence the treatment response of peginterferon plus ribavirin treatment in these patients. In the present study, we examined how ITPA and IL28B genotypes have clinical impacts on treatment-induced hematotoxicities and treatment response in HCV-infected patients treated with peginterferon plus ribavirin. ITPA genotypes (rs1127354 and rs6051702) and IL28B genotype (rs8099917) were determined by TaqMan SNP assay. We compared clinical background, treatment course and treatment response in terms of these genotypes. Only IL28B rs8099917 major type could predict sustained virological response. ITPA rs1127354 major type leads to significantly greater ribavirin-induced anemia than ITPA rs1127354 minor type between days 0 and 84. We noticed that IL28B rs8099917 minor genotype was associated with higher reduction of neutrophils and platelets. ITPA rs1127354 is useful for the prediction of ribavirin-induced anemia in the early phase after the commencement of peginterferon plus ribavirin treatment and IL28B rs8099917 is useful for the prediction of sustained virological response. Use of the combination of these two genotypes could lead to safe and effective treatment of chronic hepatitis C patients.
机译:据报道,肌苷三磷酸酶(ITPA)基因变体可预防慢性丙型肝炎患者接受利巴韦林引起的贫血。IL28B变体也影响聚乙二醇干扰素联合利巴韦林治疗这些患者的治疗反应。在本研究中,我们检查了ITPA和IL28B基因型如何对接受聚乙二醇干扰素加利巴韦林治疗的HCV感染患者的治疗引起的血液毒性和治疗反应产生临床影响。通过TaqMan SNP分析确定ITPA基因型(rs1127354和rs6051702)和IL28B基因型(rs8099917)。我们根据这些基因型比较了临床背景,治疗过程和治疗反应。只有IL28B rs8099917主要类型可以预测持续的病毒学应答。在0天到84天之间,ITPA rs1127354主要类型导致的病毒唑引起的贫血比ITPA rs1127354较小类型显着更大。我们注意到IL28B rs8099917较小基因型与中性粒细胞和血小板减少率更高有关。 ITPA rs1127354可用于在聚乙二醇干扰素加利巴韦林治疗开始后的早期预测利巴韦林引起的贫血,而IL28B rs8099917可用于预测持续的病毒学应答。结合使用这两种基因型可以安全有效地治疗慢性丙型肝炎患者。

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