Literature DB >> 31496112

HLA-DQ genotypes relative risks for celiac disease in Arabs: A case-control study.

Abdulrahman Al-Hussaini1,2, Nezar Eltayeb-Elsheikh3, Hanan Alharthi3, Awad Osman3, Maram Alshahrani1, Ibrahim Sandogji1, Sami Alrashidi1, Muhammed Salman Bashir4.   

Abstract

OBJECTIVES: It remains unknown what degree of risk is conferred by celiac disease (CD)-predisposing human leukocyte antigen (HLA)-DQ genotypes in Saudi Arabia compared with in Western countries. In this study, we aimed to determine the CD risk gradient associated with the HLA-DQ genotypes and to compare HLA-DQ genotypes between symptomatic patients with CD and screening-identified asymptomatic CD patients.
METHODS: We enrolled three groups of subjects, including 46 CD children diagnosed consecutively over the past 10 years, 54 CD children diagnosed during a mass screening of schoolchildren, and 192 healthy controls. All the participants were typed for the HLA-DQA1 and HLA-DQB1 genes by polymerase chain reaction sequence-specific oligonucleotide probes.
RESULTS: Comparing the patients with CD to controls, we identified 5 groups in the CD risk gradient: (i) very high risk associated with the DQ2.5/DQ8 genotype (odds ratio [OR] 46.93); (ii) high risk (homozygous DQ2.5, DQ2.5/DQ2.2; OR 4.12-5.04); (iii) intermediate risk (heterozygous DQ2.5, DQ8/DQ2.2; OR 1.61 and 1.67); (iv) low risk (DQ8, DQ2.2); and (v) very low risk (DQ2.x, DQX.5, DQX.x). Heterozygous DQ8 was more common in screening-identified group compared to symptomatic patients (13.0% vs 2.2%); however, other genotypes were very similar between the two groups.
CONCLUSION: The highest risk of developing CD in our Saudi Arabia population is associated with the DQ2.5/DQ8 genotype.
© 2019 Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  DQ2.2; HLA typing; HLA-DQ2.5; HLA-DQ8; Saudi Arabia; celiac disease

Mesh:

Substances:

Year:  2019        PMID: 31496112     DOI: 10.1111/1751-2980.12817

Source DB:  PubMed          Journal:  J Dig Dis        ISSN: 1751-2972            Impact factor:   2.325


  3 in total

1.  Carrier frequency of HLA-DQB1*02 allele in patients affected with celiac disease: A systematic review assessing the potential rationale of a targeted allelic genotyping as a first-line screening.

Authors:  Dimitri Poddighe; Chiara Rebuffi; Annalisa De Silvestri; Cristina Capittini
Journal:  World J Gastroenterol       Date:  2020-03-28       Impact factor: 5.742

2.  The frequency of HLA-DQ2/DQ8 haplotypes and celiac disease among the first-degree relatives of patients with celiac disease.

Authors:  Masoume Mansouri; Masoud Dadfar; Mohammad Rostami-Nejad; Golnaz Ekhlasi; Amirhossein Shahbazkhani; Bijan Shahbazkhani
Journal:  Gastroenterol Hepatol Bed Bench       Date:  2021

3.  TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls.

Authors:  Reham H Baaqeel; Babajan Banaganapalli; Hadiah Bassam Al Mahdi; Mohammed A Salama; Bakr H Alhussaini; Meshari A Alaifan; Yagoub Bin-Taleb; Noor Ahmad Shaik; Jumana Yousuf Al-Aama; Ramu Elango; Omar I Saadah
Journal:  Biosci Rep       Date:  2021-06-25       Impact factor: 3.840

  3 in total

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