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Ocul Immunol Inflamm ; 29(2): 260-263, 2021 Feb 17.
Article in English | MEDLINE | ID: mdl-32965138

ABSTRACT

PURPOSE: To determine the frequency and association of alleles at human leukocyte antigen (HLA)-DRB1 and HLA-DQB1 loci in VKH disease patients from Northern Thailand. METHODS: A case-control study was conducted with three subject groups: 23 VKH patients, 20 patients with other uveitis entities, and 40 healthy blood donors. HLA-DRB1 and HLA-DQB1 loci were analyzed and the frequency of HLA-DRB1 and HLA-DQB1 alleles was calculated by direct counting. The measure of association was calculated by odds ratio (OR) and 95% confidence interval. RESULTS: In VKH patients, the most prevalent allele was HLA-DRB1*04:05, found in 35% of patients and with the highest OR (42.13). HLA-DQB1*04:01 was the next most prevalent, found in 23.91% of VKH patients. HLA-DQB1*05:02 was also detected in 23.91% of patients; however, a higher prevalence was observed in non-VKH and healthy controls (30% and 35%, respectively). CONCLUSION: HLA-DRB1*04:05 and HLA-DQB1*04:01 could be potential genetic markers for VKH.


Subject(s)
Autoimmunity/genetics , DNA/genetics , HLA-DRB1 Chains/genetics , Uveomeningoencephalitic Syndrome/genetics , Adult , Aged , Alleles , Case-Control Studies , Female , Gene Frequency , Genetic Markers/genetics , HLA-DQ beta-Chains/genetics , HLA-DQ beta-Chains/immunology , HLA-DRB1 Chains/immunology , Histocompatibility Testing , Humans , Male , Middle Aged , Prevalence , Thailand/epidemiology , Uveomeningoencephalitic Syndrome/epidemiology , Uveomeningoencephalitic Syndrome/immunology , Young Adult
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