Akkız Hikmet, Akgöllü Ersin, Bekar Aynur, Yıldırım Selçuk, Sandıkçı Macit, Ülger Yakup, Yalınbaş Kaya Berrin, Kuran Sedef, Üsküdar Oğuz
Çukurova University, Faculty of Medicine, Department of Gastroenterology, 01330 Adana, Turkey.
Clin Res Hepatol Gastroenterol. 2015 Dec;39(6):711-7. doi: 10.1016/j.clinre.2015.02.008. Epub 2015 Apr 7.
The hepatitis C virus (HCV) which infects 3% of the world's population is a global challenge. Recently, genome-wide association studies (GWAS) have identified that the IL28B gene rs8099917 polymorphism was associated with the response to the pegylated-interferon alpha/ribavirin (PegIFNα/RBV) combination therapy in patients infected with HCV genotype 1. IL28B gene rs8099917 polymorphism should be determined before beginning treatment of HCV-infected patients to predict an individual's response. The aims of this study were to analyze the correlation between IL28B gene rs8099917 (T/G) polymorphism and PegIFNα/RBV therapy outcome in the Turkish population.
Genotypes of the IL28B gene rs8099917 (T/G) single nucleotide polymorphism (SNP) were determined in 308 patients with HCV infection by using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. One group consisted of 148 patients with a sustained virological response (SVR), whereas the second group consisted of 160 nonresponders (non-SVR).
Allele and genotype associations of IL28B gene rs8099917 polymorphism with a sustained virological response were observed in comparisons between the SVR and non-SVR groups (P<0.001). In addition, the characteristics of the subjects did not differ between these two groups except for age and fibrosis stage (P<0.05). Additionally, neither SVR nor rs80999917 genotypes were associated by HCV RNA levels.
In conclusion, the rs8099917 polymorphism was thus found strongly associated with a sustained virological response to therapy in Turkish patients infected with HCV genotype 1. Consequently, we suggest determining IL28B gene rs8099917 polymorphism of patients with HCV genotype 1 before onset of treatment.
丙型肝炎病毒(HCV)感染了全球3%的人口,是一项全球性挑战。最近,全基因组关联研究(GWAS)已确定,IL28B基因rs8099917多态性与感染丙型肝炎病毒1型的患者对聚乙二醇化干扰素α/利巴韦林(PegIFNα/RBV)联合治疗的反应相关。在开始治疗丙型肝炎病毒感染患者之前,应确定IL28B基因rs8099917多态性,以预测个体的反应。本研究的目的是分析土耳其人群中IL28B基因rs8099917(T/G)多态性与PegIFNα/RBV治疗结果之间的相关性。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法,对308例丙型肝炎病毒感染患者的IL28B基因rs8099917(T/G)单核苷酸多态性(SNP)基因型进行测定。一组由148例获得持续病毒学应答(SVR)的患者组成,而第二组由160例无应答者(非SVR)组成。
在SVR组和非SVR组的比较中,观察到IL28B基因rs8099917多态性的等位基因和基因型与持续病毒学应答之间的关联(P<0.001)。此外,除年龄和纤维化分期外,这两组受试者的特征没有差异(P<0.05)。此外,SVR和rs80999917基因型均与丙型肝炎病毒RNA水平无关。
总之,在感染丙型肝炎病毒1型的土耳其患者中,发现rs8099917多态性与治疗的持续病毒学应答密切相关。因此,我们建议在治疗开始前确定丙型肝炎病毒1型患者的IL28B基因rs8099917多态性。