Literature DB >> 26744784

The association of HLA-DRB1 and HLA-DQB1 alleles with genetic susceptibility to multiple sclerosis in the Slovak population.

Jozef Michalik1, Daniel Čierny, Ema Kantorová, Daniela Kantárová, Javor Juraj, Zuzana Párnická, Egon Kurča, Dušan Dobrota, Ján Lehotský.   

Abstract

OBJECTIVE: The aim of the present study was to assess the association between HLA-DRB1 and -DQB1 allele groups with the genetic predisposition to multiple sclerosis (MS) in the Caucasian Central European Slovak population.
METHODS: A total of 282 unrelated patients with sporadic MS were enrolled in this case-control study. HLA-DRB1 and HLA-DQB1 allele groups were genotyped using a polymerase chain reaction with sequence-specific primers. The DRB1 and DQB1 allele carrier frequencies, genotypes and haplotype frequencies were compared between MS cases and healthy controls.
RESULTS: Positive association with MS was found for alleles HLA-DRB1*15 (OR = 3.64; Pcor = 6.9x10-11), DRB1*03 (after elimination of carriers of DRB1*15, OR = 2.8; Pcor = 0.0029), DQB1*06 (OR = 1.99; Pcor = 7.0x10-4), genotypes HLA-DRB1*15/*15 (OR = 7.6; Pcor = 0.001) and DQB1*06/*06 (OR = 3.81; Pcor = 4.0x10-4) and for haplotype DRB1*15-DQB1*06 (OR = 3.03; Pcor = 0.001). Carriage of alleles DRB1*07 (OR = 0.53; Pcor = 0.04), DRB1*13 (OR = 0.39; Pcor = 4.0x10-4), DQB1*03 (OR = 0.46; Pcor = 1.0x10-4), genotypes HLA-DRB1*13/*11 (OR = 0.12; Pcor = 0.004), DQB1*05/*03 (OR = 0.39; Pcor = 0.035), DQB1*03/*03 (OR = 0.38; Pcor = 0.029) and haplotypes DRB1*13-DQB1*06 (OR = 0.47; Pcor = 0.0128) and DRB1*11-DQB1*03 (OR = 0.58; Pcor = 0.0352) was found to be protective against MS development. DISCUSSION: This is the first study performed to analyse the association of HLA-DRB1/DQB1 with susceptibility to MS in Slovakia. The results of our study confirm that HLA class II alleles, genotypes and haplotypes are associated with MS risk.

Entities:  

Keywords:  Human Leukocyte Antigen (HLA); Multiple sclerosis; Susceptibility to MS

Mesh:

Substances:

Year:  2016        PMID: 26744784     DOI: 10.1080/01616412.2015.1115212

Source DB:  PubMed          Journal:  Neurol Res        ISSN: 0161-6412            Impact factor:   2.448


  3 in total

1.  Novel Heterozygous Variants in the HLA-DRB1 Gene in a Saudi Family With Early-Onset Familial Multiple Sclerosis: Therapeutic Failure and Success.

Authors:  Hussein Algahtani; Bader Shirah; Randa Khafaji; Sarah Algahtani
Journal:  Int J MS Care       Date:  2021-10-05

2.  Human leukocyte antigen-DQB1 polymorphisms and haplotype patterns in Guillain-Barré syndrome.

Authors:  Shoma Hayat; Israt Jahan; Avizit Das; Zahid Hassan; Zakir Hossain Howlader; Ishtiaq Mahmud; Quazi Deen Mohammad; Zhahirul Islam
Journal:  Ann Clin Transl Neurol       Date:  2019-08-30       Impact factor: 4.511

3.  Alzheimer's Disease Risk Variant rs3865444 in the CD33 Gene: A Possible Role in Susceptibility to Multiple Sclerosis.

Authors:  Juraj Javor; Mária Bucová; Vladimíra Ďurmanová; Dominika Radošinská; Zuzana Párnická; Daniel Čierny; Egon Kurča; Daniela Čopíková-Cudráková; Karin Gmitterová; Ivana Shawkatová
Journal:  Life (Basel)       Date:  2022-07-21
  3 in total

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