| Autor: |
Grubic, Zorana, Maskalan, Marija, Stingl Jankovic, Katarina, Zvecic, Sabina, Dumic Kubat, Katja, Krnic, Nevena, Zunec, Renata, Dumic, Miroslav |
| Přispěvatelé: |
Steven GE Marsh |
| Jazyk: |
angličtina |
| Rok vydání: |
2017 |
| Předmět: |
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| Popis: |
The CYP21A2 mutations that are in linkage disequilibrium with particular HLA-A, -B, -DRB1 alleles/haplotypes, cause deficiency of the 21- hydroxylase enzyme (21-OHD) and account for the majority of congenital adrenal hyperplasia (CAH) cases. The aim of this study was to investigate those associations linked to the non-classical (NC) form of CAH among Croatians. The study included parents of patients with the NC form of CAH, positive for the p.V282L mutation (N =55) and cadaveric donor samples (N =231). All subjects were HLA-A, -B, and -DRB1 typed and tested for the presence of the p.V282L mutation. Among parents of patients, 92.73% of subjects were positive for the B*14:02 allele and almost half of them carried the HLA-A*33:01-B*14:02-DRB1*01:02 haplotype. Among cadaveric samples 77 out of 96 subjects positive for the B*14:02 allele had the p.V282L mutation. Among them, 37 were positive for the HLA-A*33:01- B*14:02-DRB1*01:02 haplotype, 23 had the HLA- A*33:01-B*14:02-DRB1*03:01 haplotype, 8 had the B*14:02-DRB1*01:02 combination and 5 were carrying the HLA-A*68:02-B*14:02-DRB1*13:03 haplotype. Four of these subjects were positive only for B*14:02 allele. HLA-B*14:02 was the only single allele which association with the p.V282L mutation reached statistically significant P value (RR=12.00 ; P=0.0024). Haplotypes B*14:02- DRB1*01:02 (P |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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