Eskandari E, Dahmardeh T, Safdari V, Khosravi S, Pahlevani E
Genetic of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.
Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Int J Immunogenet. 2017 Dec;44(6):322-327. doi: 10.1111/iji.12337. Epub 2017 Sep 20.
To investigate whether 14-bp Ins/Del polymorphism in HLA-G gene is associated with the risk of chronic hepatitis B (CHB) infection. This study was performed on a total of 396 individuals including 199 CHB patients and 197 healthy subjects from a south-east Iranian population. We genotyped 14-bp Ins/Del polymorphism in the HLA-G gene using polymerase chain reaction method. The results of our study revealed that the HLA-G 14-bp deletion polymorphism was associated with a reduced risk of CHB at both allele and genotypic levels. The 14-bp Del allele and Ins/Del genotype were more frequent in control group than in CHB patients (37% vs 28% for Del allele with OR = 0.68 and p-value = .015; 73% vs 52% for Ins/Del genotype with OR = 0.43 and p-value = .001) and both were protective factors against CHB. However, no difference was found in the distribution of HLA-G 14-bp genotypes among subjects with varied levels of HBV DNA or hepatic enzymes (p > .05). Our findings, for the first time, suggest that the HLA-G 14-bp Ins/Del polymorphism may be a marker for genetic susceptibility to CHB infection.
为了研究HLA - G基因中14个碱基对的插入/缺失多态性是否与慢性乙型肝炎(CHB)感染风险相关。本研究共纳入了396名个体,其中包括199名CHB患者和197名来自伊朗东南部人群的健康受试者。我们使用聚合酶链反应方法对HLA - G基因中的14个碱基对插入/缺失多态性进行基因分型。我们的研究结果显示,HLA - G基因14个碱基对缺失多态性在等位基因和基因型水平上均与CHB风险降低相关。14个碱基对缺失等位基因和插入/缺失基因型在对照组中比在CHB患者中更常见(缺失等位基因:37%对28%,OR = 0.68,p值 = 0.015;插入/缺失基因型:73%对52%,OR = 0.43,p值 = 0.001),两者均为预防CHB的保护因素。然而,在不同HBV DNA水平或肝酶水平的受试者中,HLA - G基因14个碱基对基因型的分布没有差异(p > 0.05)。我们的研究结果首次表明,HLA - G基因14个碱基对插入/缺失多态性可能是CHB感染遗传易感性的一个标志物。