TÜRKİYE POPÜLASYONUNDA HLA-DQ POLİMORFİZMLERİNİN HEPATİT B VİRÜS ENFEKSİYONU İLE İLİŞKİSİ

Bülent Çakal, M. Arıkan, Alp Atasoy, Bilger Çavuş, Mehveş Poda, Mesut Bulakçı, Mine Güllüoğlu, M. Demirci, Filiz Akyüz
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Abstract

Objective Host genetic factors can affect the natural course of hepatitis B virus (HBV) infection and the risk of development and progression of HBV-related liver diseases. The aim of this study is to evaluate the role of the HLA-DQ gene polymorphisms rs9272105, rs2856718 and rs9275572 with HBV natural clearance, viral load and the development of HBV associated liver injury. Materials and Methods The study included 150 patients with chronic hepatitis B (CHB) and 140 patients as the control group, 58 of whom had chronic hepatitis C (CHC) and 82 of whom had undergone a liver biopsy due to different clinical indications. The HLA-DQ gene rs9272105, rs2856718 and rs9275572 polymorphisms were genotypes in liver samples using the hybridization probe assay. Results A difference was found between the HLA-DQ gene rs9272105, rs2856718 and rs9275572 genotype and allele frequencies of the patients with CHB and the control group (P<0,05). The HLA-DQ rs9272105 AA genotype and presence of A allele were associated with hepatitis B surface antigen (HBsAg) clearance and liver injury (p<0,05). In contrast, the HLA-DQ genes rs2856718 and rs9275572 were not associated with HBV clearance and patients’ histological outcomes, nor with patients’ viral load, including rs9272105. Conclusions It has been suggested that the HLA-DQ rs9272105 AA genotype and the A allele are risk factors for both the persistence of HBV infection and the development of HBV-related liver damage.
目的宿主遗传因素可影响乙型肝炎病毒(HBV)感染的自然过程和HBV相关肝脏疾病的发生进展风险。本研究的目的是评估HLA-DQ基因多态性rs9272105、rs2856718和rs9275572在HBV自然清除、病毒载量和HBV相关肝损伤发生中的作用。材料与方法本研究纳入150例慢性乙型肝炎(CHB)患者和140例对照组,其中58例慢性丙型肝炎(CHC)患者和82例因不同临床指征行肝活检的患者。采用杂交探针法对肝样品中HLA-DQ基因rs9272105、rs2856718和rs9275572多态性进行基因分型。结果CHB患者HLA-DQ基因rs9272105、rs2856718和rs9275572基因型及等位基因频率与对照组差异有统计学意义(P< 0.05)。HLA-DQ rs9272105 AA基因型和A等位基因的存在与乙型肝炎表面抗原(HBsAg)清除率和肝损伤相关(p< 0.05)。相反,HLA-DQ基因rs2856718和rs9275572与HBV清除率和患者的组织学结局无关,也与患者的病毒载量无关,包括rs9272105。结论HLA-DQ rs9272105 AA基因型和A等位基因是HBV持续感染和HBV相关肝损害发生的危险因素。
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