Journals / Turkish Journal of Pediatrics / 2021 / Cilt: 63 - Sayı: 1

The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease

Pages
118–125
DOI
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⚡ TL;DR(Too Long; Didn't Read)

HLA C14, DR11, DR15, and DQ3 alleles were found to have a protective role in the same population.

📌 3 Key Takeaways

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Objective & Hypothesis:We aimed to investigate the relationship between human leukocyte antigens (HLA)-groups and clinical features, and degree of intestinal injury in children with celiac disease (CD).
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Key Findings & Data:Study group included 73 (50 females, 68.5%) children with CD.
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Conclusion & Impact:HLA C14, DR11, DR15, and DQ3 alleles were found to have a protective role in the same population.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Background. We aimed to investigate the relationship between human leukocyte antigens (HLA)-groups and clinical features, and degree of intestinal injury in children with celiac disease (CD). Methods. Study group included 73 (50 females, 68.5%) children with CD. Demographic and clinical features, accompanying autoimmune diseases, family history for CD and degree of damage in small intestinal mucosa (according to Marsh classification) at the time of diagnosis were determined. Twenty-two siblings of celiac patients without CD (15 females, 65.2%) consisted control group 1, and 66 (40 females, 60.6%) people from the normal population consisted control group 2. Results. The allele frequencies of HLA B8, B50, C6, C7, DR3, DR7, DQ2, and DR3 homozygosity were higher in the patient group. HLA DQ2 positivity was 89% in the patient group, 73.9 and 45.5% in control groups 1 and 2, respectively (p <0.0001). HLA A30, C14, DR11, DQ3 frequency were lower in patients compared to both control groups. HLA-DR15 alleles in patient and control group 1 was significantly lower compared to the general population (p <0.05). Thirty (41.1%) patients had typical, 43 (58.9%) patients had atypical presentation. Thirteen (17.8%) patients had other autoimmune diseases. There was no association between coexisting autoimmune diseases and the HLA antigens. Fifteen patients (20.5%) had a positive family history for CD; patients with HLA A69, B41 and C12 alleles had a higher positive family history (p <0.05). Intestinal mucosal damage was as follows: 5 patients (6.8%) had Marsh 2, 25 (34.3%) Marsh 3a, 28 (38.4%) Marsh 3b, 15 (20.5%) Marsh 3c. Patients with HLA-DR15 alleles had more frequent Marsh 3a lesions (p <0.05). Conclusions. B8, B50, C6, C7, DR3, DR7, DR3/DR3, DQ2 alleles were risk factors for CD in the Turkish population. HLA C14, DR11, DR15, and DQ3 alleles were found to have a protective role in the same population.

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Cite This Article

Balamtekin, N., BAYSOY, G., KIZILKAN, N. U., DEMIR, H., TEMİZEL, İ. N. S., ÖZEN, H., YÜCE, A., GÜRAKAN, F., TAN, Ç., TEZCAN, İ. (2021). The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease. Turkish Journal of Pediatrics, Cilt: 63 - Sayı: 1, 118–125. https://ajindex.com/articles/411744

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References (15)

  1. NIH Consensus Statement on Celiac Disease. NIH Consens State Sci Statements 2004; 21: 1-23
  2. Lebwohl B, Sanders DS, Green PHR. Coeliac disease. Lancet 2018; 391: 70-81
  3. Brown JRG, Singh P. Coeliac disease. Paediatr Int Child Health 2019; 39: 23-31
  4. Hill ID, Dirks MH, Liptak GS, et al; North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Guideline for diagnosis and treatment of celiac disease in children: Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr 2005; 40: 1-19
  5. Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition. Arch Dis Child 1990; 65: 909-911
  6. Ryan AW, Thornton JM, Brophy K, et al. Chromosome 5q candidate genes in coeliac disease: genetic variation at IL4, IL5, IL9, IL13, IL17B and NR3C1. Tissue Antigens 2005; 65: 150-155
  7. Bolognesi E, Karell K, Percopo S, et al. Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease. Tissue Antigens 2003; 61: 308-316
  8. Louka AS, Sollid LM. HLA in coeliac disease: unravelling the complex genetics of a complex disorder. Tissue Antigens 2003; 61: 105-117
  9. Louka AS, Moodie SJ, Karell K, et al; European Genetics Cluster on Celiac Disease. A collaborative European search for non-DQA1*05-DQB1*02 celiac disease loci on HLA-DR3 haplotypes: analysis of transmission from homozygous parents. Hum Immunol 2003; 64: 350-358
  10. Tümer L, Altuntaş B, Hasanoglu A, Söylemezoglu O, Arinsoy T. Pattern of human leukocyte antigens in Turkish children with celiac disease. Pediatr Int 2000; 42: 678-681
  11. Tüysüz B, Dursun A, Kutlu T, et al. HLA-DQ alleles in patients with celiac disease in Turkey. Tissue Antigens 2001; 57: 540-542
  12. Erkan T, Kutlu T, Yılmaz E, Cullu F, Tümay T. Human leukocyte antigens in Turkish pediatric celiac patients. Turk J Pediatr 1999; 41: 181-188
  13. Kuloğlu Z, Doğancı T, Kansu A, et al. HLA types in Turkish children with celiac disease. Turk J Pediatr 2008; 50: 515-520
  14. Basturk A, Artan R, Yılmaz A. The incidence of HLADQ2/DQ8 in Turkish children with celiac disease and a comparison of the geographical distribution of HLA-DQ. Prz Gastroenterol 2017; 12: 256-261
  15. Megiorni F, Mora B, Bonamico M, et al. HLA-DQ and susceptibility to celiac disease: evidence for gender differences and parent-of-origin effects. Am J Gastroenter