白细胞介素28B基因多态性与拉脱维亚慢性丙型肝炎治疗结果的关系

Hepatitis research and treatment Pub Date : 2012-01-01 Epub Date: 2012-04-24 DOI:10.1155/2012/324090
Ieva Tolmane, Baiba Rozentale, Jazeps Keiss, Ludmila Ivancenko, Nadezda Subnikova, Zaiga Reinholde, Ieva Kozlovska, Nina Sumlaninova, Sniedze Laivacuma, Raimonds Simanis
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引用次数: 18

摘要

介绍。在慢性丙型肝炎的标准治疗中,只有一半的患者能够实现持续的病毒学反应(SVR)。白细胞介素- 28b似乎参与了HCV感染的控制,编码IL-28B基因的遗传多态性可能决定了清除HCV的效果。本文的目的是检测拉脱维亚IL-28B基因多态性并分析治疗结果。这是拉脱维亚首次对IL-28B基因多态性进行研究。材料和方法。该研究包括159名慢性病毒性丙型肝炎患者。为了检测IL-28B基因多态性,我们采用了分子生物学技术和方法:经典DNA分离、PCR扩增和标准测序。基因型定义为CC、CT、TC或TT型。142例患者接受标准护理治疗。结果根据IL-28B多态性进行分析。结果。CC基因型53例(33%),CT/TC基因型84例(53%),TT基因型22例(14%)。CC基因型亚组34例(74%)患者达到SVR,非CC基因型亚组50例(52%)患者达到SVR。在基因型为1的患者中,CC亚组中有16例患者(84%)达到SVR,而非CC亚组中有30例患者(47.6%)达到SVR, P = 0.007。结论。拉脱维亚IL28B最常见的基因型为CT/TC,发病率为53%。CC基因型患者比CT或TT亚组更容易达到SVR。因此,IL28B基因多态性是治疗结果的一个强有力的预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Interleukin 28B Gene Polymorphism and Association with Chronic Hepatitis C Therapy Results in Latvia.

Introduction. With the standard treatment of chronic hepatitis C, sustained virological response (SVR) can be achieved only in half of all patients. Interleukin-28B appears to be involved in the control of HCV infection, and the genetic polymorphism of the encoding IL-28B gene may determine the efficacy of clearance of HCV. The aim of this paper was to detect IL-28B gene polymorphism in Latvia and to analyze therapy results. This is the first study on IL-28B gene polymorphism in Latvia. Material and Methods. There were 159 chronic viral hepatitis C patients included in the study. In order to detect IL-28B gene polymorphism, we used molecular biology techniques and methods: classical DNA separation, amplification by PCR, and standard sequencing. Genotype was defined as CC, CT, TC, or TT type. 142 patients were treated with the standard of care treatment. Results were analyzed according to IL-28B polymorphism. Results. There were 53 patients (33%) with CC genotype, 84 patients (53%) with CT/TC genotype, and 22 patients (14%) with TT genotype. 34 patients (74%) in CC genotype subgroup achieved SVR versus 50 patients (52%) in non-CC subgroups. In patients with genotype 1, SVR was achieved in 16 patients (84%) in CC subgroup versus 30 patients (47.6%) in non-CC subgroups, P = 0.007. Conclusions. The most common genotype of IL28B in Latvia is CT/TC, with an incidence of 53%. Patients with CC genotype achieved SVR more often than CT or TT subgroups. IL28B gene polymorphism therefore is a strong predictor of treatment result.

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