Allele and haplotype frequencies for HLA-DQ in Iranian celiac disease patients

被引:29
|
作者
Rostami-Nejad, Mohammad [1 ]
Romanos, Jihane [2 ,6 ]
Rostami, Kamran [3 ]
Ganji, Azita [4 ]
Ehsani-Ardakani, Mohammad Javad [1 ]
Bakhshipour, Ali-Reza [5 ]
Zojaji, Homayoun [1 ]
Mohebbi, Seyed Reza [1 ]
Zali, Mohammad-Reza [1 ]
Wijmenga, Cisca [2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Gastroenterol & Liver Dis Res Ctr, Dept Celiac Dis, Tehran 1985717411, Iran
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands
[3] Worcestershire Royal Hosp, Dept Gastroenterol, Worcester WR5 1DD, England
[4] Mashhad Univ Med Sci, Imam Reza Hosp, Dept Gastroenterol, Mashhad 1351143, Iran
[5] Zahedan Univ Med Sci, Dept Gastroenterol, Zahedan 2143453, Iran
[6] Lebanese Amer Univ, Inst Human Genet, Dept Genet, Byblos 36, Lebanon
基金
美国国家科学基金会;
关键词
Human leukocyte antigen typing; Validation; Susceptibility; Celiac disease; Iran; RISK; PATHOGENESIS; ASSOCIATION; PREVALENCE; DIAGNOSIS;
D O I
10.3748/wjg.v20.i20.6302
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To assess the distribution of human leukocyte antigen (HLA)-DQ2 and -DQ8 in Iranian celiac disease (CD) patients and compare them to healthy Iranian controls. METHODS: To predict the HLA-DQA1 and -DQB1 genes, we used six previously reported HLA-tagging single nucleotide polymorphism to determine HLA genotypes in 59 Iranian patients with 'biopsy-confirmed' CD and in 151 healthy Iranian individuals. To test the transferability of the method, 50 cases and controls were also typed using a commercial kit that identifies individual carriers of DQ2, DQ7 and DQ8 alleles. RESULTS: In this pilot study 97% of CD cases (n = 57) and 58% of controls (n = 87) were carriers of HLA-DQ2 and/or HLA-DQ8 heterodimers, either in the homozygous or heterozygous state. The HLA-DQ pattern of these 57 CD patients: heterozygous DQ2.2 (n = 14) and homozygous DQ2.2 (n = 1), heterozygous DQ2.5 (n = 33) and homozygous DQ2.5 (n = 8), heterozygous DQ8 (n = 13) and homozygous DQ8 (n = 2). Two CD patients were negative for both DQ2 and DQ8 (3%). CONCLUSION: The prevalence of DQ8 in our CD population was higher than that reported in other populations (25.4%). As reported in other populations, our results underline the primary importance of HLA-DQ alleles in the Iranian population's susceptibility to CD. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:6302 / 6308
页数:7
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