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白细胞介素-18 基因多态性与中国汉族高危人群丙型肝炎病毒感染结局的相关性。

Association of interleukin-18 gene polymorphisms with the outcomes of hepatitis C virus infection in high-risk Chinese Han population.

机构信息

School of Life Science and Technology, China Pharmaceutical University, No. 24 Tongjiaxiang, Nanjing 210009, Jiangsu, China.

出版信息

Immunol Lett. 2013 Jul-Aug;154(1-2):54-60. doi: 10.1016/j.imlet.2013.08.007. Epub 2013 Aug 23.

Abstract

Interleukin 18 (IL-18) gene polymorphisms have been reported to be associated with the outcomes of hepatitis C virus (HCV) infection in Americans, Indians and Europeans. We aimed to investigate whether the association can be replicated in Chinese Han population. Three IL-18 variants, -656G>T, -137G>C and +105A>C, were genotyped in three independent Han cohorts consisting of 552 cases and 784 controls. By using logistic regression analysis and multiple testing, haplotype GCC were associated with a protection from susceptibility to HCV. After stratified analysis, both the carriage of -137C allele in the older or hemodialysis subgroup and the carriage of +105C allele in the younger subgroup were found to be significantly associated with a decreased risk of HCV susceptibility. By using logistic regression analysis and multiple testing for the resolution of HCV infection, our study showed that +105C allele and haplotype GGC displayed a negative effect on HCV persistence. After stratified analysis, a significantly decreased risk for HCV persistence was found in +105C allele in the subgroups of young, male or female, drug user or hemodialysis and HCV-1 or HCV mixed genotype. No significant association was observed between -656G>T and the outcomes of HCV infection. Our results demonstrated that the carriage of -137C allele, +105C allele, haplotype -656G/-137C/+105C and haplotype -656G/-137G/+105C of IL-18 gene may contribute to better outcomes of HCV infection in high-risk Chinese Han population.

摘要

白细胞介素 18 (IL-18) 基因多态性与丙型肝炎病毒 (HCV) 感染在美国、印度和欧洲人群中的结局相关。我们旨在研究这种关联是否可以在中国汉族人群中得到复制。在三个独立的汉族队列中,对三个 IL-18 变体(-656G>T、-137G>C 和 +105A>C)进行了基因分型,包括 552 例病例和 784 例对照。通过使用逻辑回归分析和多重检验,发现 GCC 单倍型与对 HCV 易感性的保护作用相关。经过分层分析,发现 -137C 等位基因在老年或血液透析亚组中的携带以及 +105C 等位基因在年轻亚组中的携带与 HCV 易感性降低显著相关。通过使用逻辑回归分析和 HCV 感染消退的多重检验,我们的研究表明 +105C 等位基因和 GGC 单倍型对 HCV 持续存在显示出负面影响。经过分层分析,在年轻、男性或女性、药物使用者或血液透析以及 HCV-1 或 HCV 混合基因型亚组中,+105C 等位基因显著降低了 HCV 持续存在的风险。-656G>T 与 HCV 感染的结局之间未观察到显著关联。我们的结果表明,IL-18 基因的 -137C 等位基因、+105C 等位基因、-656G/-137C/+105C 单倍型和 -656G/-137G/+105C 单倍型的携带可能有助于高危中国汉族人群中 HCV 感染的更好结局。

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