Comparative analysis of HLA II allele and genotype frequency distribution in patients with type 1 diabetes mellitus and autoimmune thyroiditis
Author(s) -
Ekaterina Alexandrovna Repina,
Т М Атаманова,
Yana Stanislavovna Zvereva,
Yulia Vladimirovna Tishina,
Sergey Alexandrovich Prokof'ev
Publication year - 2013
Publication title -
diabetes mellitus
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.155
H-Index - 12
eISSN - 2072-0378
pISSN - 2072-0351
DOI - 10.14341/dm2013423-27
Subject(s) - genotyping , genotype , medicine , autoimmune thyroiditis , allele , thyroiditis , immunology , human leukocyte antigen , hla dq , comorbidity , allele frequency , diabetes mellitus , type 1 diabetes , gastroenterology , thyroid , endocrinology , genetics , gene , biology , haplotype , antigen
Aim. To compare HLA II allele and genotype frequency distribution in type 1 diabetes mellitus (T1DM) and autoimmune thyroiditis (AIT) with that in isolated T1DM. Materials and Methods. A total of 92 T1DM patients were subdivided into two groups. The first group comprised 54 patients with established AIT comorbidity or elevation of anti-thyroid autoantibodies (ATA). Patients with isolated T1DM (ATA-negative) formed the second group. HLA-genotyping was performed by multiprimer PCR set for the three following genes: DRB1 , DQA1 and DQВ1 . Results. Prevalence of alleles DRB1 *01, *03(017), *04, *07, *11 and genotypes 01/03, 01/04, 03/04 tends to be higher among patients with AIT comorbidity. The comorbidity group was also characterized by the trend towards higher prevalence of ?marker/marker? and ?marker/non-marker? combinations favouring the former variant. Conversely, ATA-negative patients exhibited trend for higher prevalence of ?non-marker/non-marker? combination. Conclusion. Statistically insignificant difference between HLA II alleles and genotypes in the two studied groups suggests that primary genetic factors are common in these two diseases. Plausibly, genes other than DRB1 , DQA1 and DQВ1 determine the localization of the autoimmune process.
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