Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9280
Title: HLA genotyping in pediatric celiac disease patients
Authors: Stankovic, BIljana
Radlovic N.
Leković Z.
Ristic Medic D.
Radlović V.
Nikčević G.
Kotur, Nikola
Vucicevic, Ksenija
Kostic N.
Pavlovic G.
Zukic B.
Journal: Bosnian Journal of Basic Medical Sciences
Issue Date: 1-Jan-2015
Abstract: © 2014 ABMSFBIH Celiac disease (CD) is a chronic inflammatory disease in the small intestine triggered by gluten uptake that occurs in genetically susceptible individuals. HLA-DQ2 protein encoded by HLA-DQA1*05 and DQB1*02 alleles is found in 90-95% of CD patients. All of the remaining patients carry HLA-DQ8 protein encoded by HLA-DQA1*03 and DQB1*03:02 alleles. Specific HLA-DQ genotypes define different risk for CD incidence. Presence of susceptible HLA-DQ genotypes does not predict certain disease development, but their absence makes CD very unlikely, close to 100%. Here we presented for the first time the distribution of HLA-DQ genotypes in the group of pediatric celiac patients from the University Children’s Hospital, Belgrade, Serbia and estimated risk for CD development that these genotypes confer. Seventy three celiac disease patients and 62 healthy individuals underwent genotyping for DQA1, DQB1 alleles and DRB1 allele. 94.5% of patients carried alleles that encode DQ2 protein variant and 2.7% carried alleles that encode DQ8 protein variant. Two patients carried single DQB1*02 allele. No patients were negative for all the alleles predisposing to CD. The highest HLA-DQ genotype risk for CD development was found in group of patients homozygous for DQ2.5 haplotype, followed by the group of heterozygous carriers of DQ2.5 haplotype in combination with DQB1*02 allele within the other haplotype. The lowest risk was observed in carriers of a single copy of DQB1*02 or DQA1*05 allele or other non-predisposing alleles. HLA genotyping, more informative than serological testing commonly used, proved to be a useful diagnostic tool for excluding CD development.
URI: https://scidar.kg.ac.rs/handle/123456789/9280
Type: Article
DOI: 10.17305/bjbms.2014.3.28
ISSN: 15128601
SCOPUS: 84928229946
Appears in Collections:Faculty of Medical Sciences, Kragujevac
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