Literature DB >> 12757179

Distribution of HLA class I alleles differs in celiac disease patients according to age of onset.

Harald Vogelsang1, Simon Panzer, Wolfgang R Mayr, Gerhard Granditsch, Gottfried F Fischer.   

Abstract

Celiac disease (CD) or gluten-sensitive enteropathy is strongly associated with HLA-DQ alleles; more than 95% of patients are DQB1*02. However, the uniform association with HLA-DQ alleles does not explain the clinical heterogeneity, especially the wide range in the age of onset of CD. We asked whether the age of onset of CD is also influenced by class I genes of the human MHC. We performed HLA typing in three groups of patients suffering from CD. The age of onset in the first group (N = 200) was before 15 years of age, in the second group (N = 62) between 15 and 40 years, in the third group (N = 59) after 40 years. We observed a statistically significant increase in the frequencies of HLA-B8 and Cw7 with increasing age of onset. In conclusion, we conclude that distinct alleles from the class I region of the human MHC might lead to late onset of CD. In particular, relatives of CD patients with the disease-prone HLA class I alleles HLA-B8 and Cw7 should be followed up carefully for late onset of CD.

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Year:  2003        PMID: 12757179     DOI: 10.1023/a:1022517606512

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  22 in total

Review 1.  Role of tissue transglutaminase in celiac disease.

Authors:  O Molberg; S N McAdam; L M Sollid
Journal:  J Pediatr Gastroenterol Nutr       Date:  2000-03       Impact factor: 2.839

2.  Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium.

Authors: 
Journal:  Nature       Date:  1999-10-28       Impact factor: 49.962

Review 3.  Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition.

Authors: 
Journal:  Arch Dis Child       Date:  1990-08       Impact factor: 3.791

4.  HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides.

Authors:  F Clot; C Gianfrani; M C Babron; F Bouguerra; S Southwood; M F Kagnoff; R Troncone; S Percopo; J F Eliaou; F Clerget-Darpoux; A Sette; L Greco
Journal:  Immunogenetics       Date:  1999-08       Impact factor: 2.846

Review 5.  HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis.

Authors:  L M Sollid; E Thorsby
Journal:  Gastroenterology       Date:  1993-09       Impact factor: 22.682

6.  A combination of two distinct in vitro amplification procedures for DNA typing of HLA-DRB and -DQB 1 alleles.

Authors:  G F Fischer; I Faé; M Petrasek; S Moser
Journal:  Vox Sang       Date:  1995       Impact factor: 2.144

7.  Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease. SIGEP Study Group for Autoimmune Disorders in Celiac Disease.

Authors:  A Ventura; G Magazzù; L Greco
Journal:  Gastroenterology       Date:  1999-08       Impact factor: 22.682

8.  A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease.

Authors:  B A Lie; L M Sollid; H Ascher; J Ek; H E Akselsen; K S Rønningen; E Thorsby; D E Undlien
Journal:  Tissue Antigens       Date:  1999-08

9.  Effect of diet and age on jejunal and circulating lymphocyte subsets in children with coeliac disease: persistence of CD4-8-intraepithelial T cells through treatment.

Authors:  M A Verkasalo; A Arató; E Savilahti; V M Tainio
Journal:  Gut       Date:  1990-04       Impact factor: 23.059

10.  Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer.

Authors:  L M Sollid; G Markussen; J Ek; H Gjerde; F Vartdal; E Thorsby
Journal:  J Exp Med       Date:  1989-01-01       Impact factor: 14.307

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