伊朗东北部结节病患者白细胞抗原- drb1等位基因分析

Z. Mirfeizi, M. Sahebari, S. Nabavi, Masoumeh Salari, Masoud Saghafi, Z. Rezaieyazdi, N. Valizadeh, Houshang Raaftpanah
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引用次数: 1

摘要

结节病是一种病因不明、临床表现各异的系统性肉芽肿性疾病。HLA基因,特别是HLA- drb1,已被证明是结节病病因的候选基因。本研究探讨了伊朗人HLA-DRB1等位基因多态性与结节病之间的关系。研究人群包括58例结节病患者和68例健康对照。提取基因组DNA,采用序列特异性引物聚合酶链反应(PCR-SSP)测定HLA-DRB1等位基因多态性。结节病患者HLA-DRB1*07的表达频率(25.8%)高于对照组(15.3%);两组间差异无统计学意义(P>0.05)。HLA-DRB1*11阳性率对照组(31.9%)高于对照组(22.4%),组间差异无统计学意义(P>0.05)。本研究结果表明,在伊朗东北部马什哈德,HLA-DRB1等位基因与结节病易感性之间没有关联。为了澄清这个问题,需要进一步的大样本研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human leukocyte antigen-DRB1 alleles in patients with sarcoidosis from Northeast Iran
Sarcoidosis a systemic granulomatous disorder of unknown etiology with varying clinical pictures. HLA genes, especially HLA-DRB1, have been shown to be candidates for the etiology of sarcoidosis. This study examined the association between the polymorphism of HLA-DRB1 alleles and sarcoidosis in Iranian subjects. The study population included 58 patients with sarcoidosis and 68 healthy controls. Genomic DNA was extracted, and the polymorphisms of the HLA-DRB1 alleles were determined using a polymerase chain reaction with sequence-specific primer (PCR-SSP). The frequency of HLA-DRB1*07 was higher in sarcoidosis patients (25.8%) than in controls (15.3%); however no significant difference was observed between the two groups (P>0.05). The frequency of HLA-DRB1*11 was higher in the control group (31.9%) than in cases (22.4%), but no significant difference was detected between the groups (P>0.05). The results of the present study showed that there is no association between HLA-DRB1 alleles and susceptibility to sarcoidosis in Mashhad, Northeast Iran. Further studies with large sample sizes are required in order to clarify this issue.
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