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Z Jurcić1, L Brkljacić-Surkalović, Z Grubić
1Klinika za djecje bolesti, KB Sestre milosrdnice, Zagreb.
Insights
Coeliac disease (CD) in Croatia is strongly linked to specific human leukocyte antigen (HLA) types, particularly HLA-DQ2. This study confirms HLA-DQ2 as a key genetic marker for coeliac disease in the Croatian population.
Area of Science:
- Immunogenetics
- Human Leukocyte Antigen (HLA) complex
- Gastroenterology
Context:
- Coeliac disease (CD) exhibits one of the strongest known associations with class II HLA genes.
- Previous studies have not investigated HLA antigen and haplotype frequencies in Croatian CD patients.
Purpose:
- To determine the prevalence of HLA-DR and HLA-DQ antigens and common HLA-DR-DQ haplotypes in Croatian patients with coeliac disease.
- To establish the genetic landscape of CD in Croatia.
Summary:
- A study of 58 biopsy-proven coeliac disease patients and control groups (502 for HLA-DR, 118 for HLA-DQ) utilized standard microcytotoxicity assays.
- High frequencies of HLA-DR3 (84.48%) and HLA-DQ2 (96.55%) were observed in CD patients. Homozygosity for DQ2 was significantly increased (25.86% in patients vs. 2.87% in controls).
- The DR3-DQ2 haplotype was identified as the primary genetic association with coeliac disease in Croatia.
Impact:
- This research provides crucial genetic data for coeliac disease in Croatia, a region previously lacking such information.
- The findings reinforce the role of specific HLA class II alleles, particularly HLA-DQ2, in coeliac disease susceptibility.
- Establishes a foundation for future genetic research and potential diagnostic strategies for coeliac disease in the Croatian population.
Objectives:
Coeliac disease (CD) has one of the strongest class II HLA association of any human disease. The goal of this study was to establish the frequency of HLA-DR and DQ antigens, as well as common HLA-DR-DQ haplotypes among CD patients. No similar study has previously been done in Croatian patients.
Patients And Controls:
There were 58 biopsy proven patients with CD. The control groups comprised 502 and 118 healthy person for HLA-DR and HLA-DQ typing, respectively.
Methods:
The class II HLA-DR and DQ antigens typing were carried out by standard microcytotoxicity assay for B cells. Only antisera to three specificities (DQ1, 2 and 3) were available to us at the time of the study.
Results:
We confirmed the high frequency of HLA-DR3 (84.48%; RR = 23.7; p < 0.00001) in our patients with CD. As reported in other populations, most of the patients negative for DR3, were heterozygous for DR7 and DR5 (10.34%) or DR4/DR5, DR4/DR6 (3.44%). CD was significantly correlated with the presence of HLA-DQ2 (96.55%, RR = 75.9; p < 0.00001). Correlation with CD was strongly dependent on homozygosity, 15 out of 58 (25.86%) of the patients and 4 (2.87%) of the controls being homozygotes for DQ2 (RR = 11.9; p < 0.00001). The remaining two patients were DR4-DQ3 positive. Among extended haplotypes only DR2-DQ1 was under-represented (RR = 0.3; p < 0.0033).
Conclusion:
The results suggest that in Croatia CD is primarily associated with HLA-DQ2 specificities on the DR3-DQ2 haplotype.
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