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The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease
AIM: The aim of this study was to evaluate the likelihood ratio and frequency of DQ2 and DQ8 in Iranian patients with celiac disease (CD). BACKGROUND: The HLA DQ2 and HLA DQ8 are the important mediators in the development of celiac disease. A few studies evaluated the frequency of HLA DQ2 and HLA DQ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702037/ https://www.ncbi.nlm.nih.gov/pubmed/26744610 |
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author | Khosravi, Asghar Mansouri, Masoume Rostami-Nejad, Mohammad Shahbazkhani, Bijan Ekhlasi, Golnaz Kalantari, Ebrahim |
author_facet | Khosravi, Asghar Mansouri, Masoume Rostami-Nejad, Mohammad Shahbazkhani, Bijan Ekhlasi, Golnaz Kalantari, Ebrahim |
author_sort | Khosravi, Asghar |
collection | PubMed |
description | AIM: The aim of this study was to evaluate the likelihood ratio and frequency of DQ2 and DQ8 in Iranian patients with celiac disease (CD). BACKGROUND: The HLA DQ2 and HLA DQ8 are the important mediators in the development of celiac disease. A few studies evaluated the frequency of HLA DQ2 and HLA DQ8 haplotypes among the Iranian population with low sample size. PATIENTS AND METHODS: In this cross-sectional study, to predict HLA–DQ2 and DQ8 haplotypes, 141(73 male, 78 female) confirmed CD patients compared to 151 healthy controls were enrolled into this study during 2013-2014. HLA DQ2/ DQ8 haplotypes was determined in cases and controls using PCR-SSP technique. RESULTS: DQ2 and DQ8 were positive in 80% (n=111) and 49% (n= 69) of CD patients and 36% (n=61) and 13% (n=21) of control group respectively. Moreover, 32% (n=45) of CD patients and 5.3% (n=8) of the control group were carrier of both haplotypes. In the case group about one-third of patients (32.2%) were positive for carrying both DQ2 and DQ8 heterodimers while only 5.3% (n=8) of the control group were carrier. In addition, the positive likelihood ratio of DQ2 and DQ8 were 1.74 (CI: 1.4- 2.1), and 2.6 (CI: 1.8– 2.7), respectively. CONCLUSION: The result of this study showed that the frequency of DQ8 among our population is higher than those reported by European countries, but it is close to those founded in South America and Middle East. This result suggests that the higher prevalence of HLA DQ8 pattern in Iranian CD patients is similar to non-European patients. |
format | Online Article Text |
id | pubmed-4702037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-47020372016-01-07 The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease Khosravi, Asghar Mansouri, Masoume Rostami-Nejad, Mohammad Shahbazkhani, Bijan Ekhlasi, Golnaz Kalantari, Ebrahim Gastroenterol Hepatol Bed Bench Original Article AIM: The aim of this study was to evaluate the likelihood ratio and frequency of DQ2 and DQ8 in Iranian patients with celiac disease (CD). BACKGROUND: The HLA DQ2 and HLA DQ8 are the important mediators in the development of celiac disease. A few studies evaluated the frequency of HLA DQ2 and HLA DQ8 haplotypes among the Iranian population with low sample size. PATIENTS AND METHODS: In this cross-sectional study, to predict HLA–DQ2 and DQ8 haplotypes, 141(73 male, 78 female) confirmed CD patients compared to 151 healthy controls were enrolled into this study during 2013-2014. HLA DQ2/ DQ8 haplotypes was determined in cases and controls using PCR-SSP technique. RESULTS: DQ2 and DQ8 were positive in 80% (n=111) and 49% (n= 69) of CD patients and 36% (n=61) and 13% (n=21) of control group respectively. Moreover, 32% (n=45) of CD patients and 5.3% (n=8) of the control group were carrier of both haplotypes. In the case group about one-third of patients (32.2%) were positive for carrying both DQ2 and DQ8 heterodimers while only 5.3% (n=8) of the control group were carrier. In addition, the positive likelihood ratio of DQ2 and DQ8 were 1.74 (CI: 1.4- 2.1), and 2.6 (CI: 1.8– 2.7), respectively. CONCLUSION: The result of this study showed that the frequency of DQ8 among our population is higher than those reported by European countries, but it is close to those founded in South America and Middle East. This result suggests that the higher prevalence of HLA DQ8 pattern in Iranian CD patients is similar to non-European patients. Shaheed Beheshti University of Medical Sciences 2016 /pmc/articles/PMC4702037/ /pubmed/26744610 Text en ©2016 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khosravi, Asghar Mansouri, Masoume Rostami-Nejad, Mohammad Shahbazkhani, Bijan Ekhlasi, Golnaz Kalantari, Ebrahim The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title | The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title_full | The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title_fullStr | The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title_full_unstemmed | The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title_short | The likelihood ratio and frequency of DQ2/DQ8 haplotypes in Iranian patients with celiac disease |
title_sort | likelihood ratio and frequency of dq2/dq8 haplotypes in iranian patients with celiac disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702037/ https://www.ncbi.nlm.nih.gov/pubmed/26744610 |
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