Lu Yu, Bao Jin-Gui, Deng Yan, Rong Cheng-Zhi, Liu Yan-Qiong, Huang Xiu-Li, Song Liu-Ying, Li Shan, Qin Xue
Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China E-mail :
Asian Pac J Cancer Prev. 2015;16(14):6019-26. doi: 10.7314/apjcp.2015.16.14.6019.
The aim of this study was to assess the relationship between IL-18 gene polymorphisms and HBV-related diseases and whether these polymorphisms influence its expression in the Guangxi Zhuang population.
We enrolled 129 chronic HBV infected (CHB) patients, 86 HBV-related liver cirrhosis (LC) patients and 160 healthy controls in our study. Polymerase chain reaction-restriction fragment length polymorphism methods were used to detect IL-18 gene -607C/A, -137G/C polymorphisms, and an ELISA kit was employed to determine serum IL-18 levels.
No correlation was found between the -607C/A polymorphism and risk of HBV-related disease. For the -137G/C polymorphism, the GC genotype and C allele were associated with a significantly lower risk of CHB (95%CI: 0.32-0.95, p=0.034 and 95%CI: 0.35-0.91, p=0.018) and HBV-related LC (95%CI: 0.24-0.89, p=0.022 and 95%CI: 0.28-0.90, p=0.021). A similar decreased risk was also found with the A-607C-137 haplotype. With respect to IL-18 expression, it was significantly lower in both patient groups, but no association was noted between the two polymorphisms in the IL-18 gene and its expression.
Our study indicated that the -137C allele in the IL-18 gene may be a protective factor for HBV-related disease, and serum IL-18 level may be inversely associated with CHB and HBV-related LC.
本研究旨在评估白细胞介素-18(IL-18)基因多态性与乙型肝炎病毒(HBV)相关疾病之间的关系,以及这些多态性是否影响其在广西壮族人群中的表达。
本研究纳入了129例慢性HBV感染(CHB)患者、86例HBV相关肝硬化(LC)患者和160例健康对照。采用聚合酶链反应-限制性片段长度多态性方法检测IL-18基因-607C/A、-137G/C多态性,并使用酶联免疫吸附测定试剂盒测定血清IL-18水平。
未发现-607C/A多态性与HBV相关疾病风险之间存在相关性。对于-137G/C多态性,GC基因型和C等位基因与CHB(95%置信区间:0.32-0.95,p=0.034;95%置信区间:0.35-0.91,p=0.018)和HBV相关LC(95%置信区间:0.24-0.89,p=0.022;95%置信区间:0.28-0.90,p=0.021)的风险显著降低相关。A-607C-137单倍型也发现了类似的风险降低。关于IL-18表达,两组患者的表达均显著降低,但IL-18基因的两种多态性与其表达之间未发现关联。
我们的研究表明,IL-18基因中的-137C等位基因可能是HBV相关疾病的保护因素,血清IL-18水平可能与CHB和HBV相关LC呈负相关。