Literature DB >> 21593645

HLA-DQ genotyping combined with serological markers for the diagnosis of celiac disease: is intestinal biopsy still mandatory?

Haude Clouzeau-Girard1, Laurent Rebouissoux, Jean-Luc Taupin, Brigitte Le Bail, Nicolas Kalach, Laurent Michaud, Alain Dabadie, Jean-Pierre Olives, Patrick Blanco, Alain Morali, Jean-François Moreau, Thierry Lamireau.   

Abstract

OBJECTIVES: The aim of this study was to evaluate the value of HLA-DQ2/DQ8 allelic genotyping combined with serologic testing for the diagnosis of celiac disease (CD). PATIENTS AND METHODS: One hundred seventy children, who underwent jejunal biopsy for digestive symptoms or malnutrition, were tested for HLA-DQ2/DQ8 and serologic markers (tTG and/or anti-endomysial antibodies). Children were classified in 2 groups, according to jejunal histology: group 1, when partial or total villous atrophy was associated with an increased intraepithelial lymphocytosis suggesting CD, and group 2, when these histological criteria were absent.
RESULTS: Eight children were excluded from the study because their intestinal histology was not informative; 82 children were classified in group 1 and 80 in group 2. Eighty-one of 82 children in group 1 were positive for HLA and serologic testing. The other child had negative HLA and serologic testing but marked villous atrophy, and further investigation showed an allergic disease. Among the 80 children in group 2, 53 were negative for both HLA and serologic testing, 22 were positive for HLA but negative for serologic testing, 2 were negative for HLA and positive for serologic testing, and 3 patients were positive for both HLA and serologic testing. The last 3 children were shown to have an autoimmune background and had probably a latent form of CD. The association of HLA-DQ2/DQ8 and serologic markers had a sensitivity of 98.8%, a specificity of 96.2%, a positive likelihood ratio of 26.3, and a negative likelihood ratio of 0.013.
CONCLUSIONS: The association of positive HLA-DQ2/DQ8 and serologic testing has a high predictive value for CD. We suggest that symptomatic children with high titers of immunoglobulin (Ig)A tTG could be diagnosed as patients with CD without performing jejunal biopsy. In other children, HLA-DQ2/DQ8 could be useful to exclude the diagnosis of CD if negative. In cases of low IgA tTG titers or in patients with IgA deficiency, intestinal biopsy remains mandatory.

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Year:  2011        PMID: 21593645     DOI: 10.1097/MPG.0b013e31820a724d

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  8 in total

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3.  Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population.

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4.  Clinical utility of celiac disease-associated HLA testing.

Authors:  Kumar Pallav; Toufic Kabbani; Sohaib Tariq; Rohini Vanga; Ciaran P Kelly; Daniel A Leffler
Journal:  Dig Dis Sci       Date:  2014-04-06       Impact factor: 3.199

5.  Phenotypical characterization of the peripheral blood T cells in patients with celiac disease: does it differentiate suspicious celiac disease cases?

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6.  Omitting duodenal biopsy in children with suspected celiac disease and extra-intestinal symptoms.

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Journal:  Ital J Pediatr       Date:  2017-07-15       Impact factor: 2.638

Review 7.  The serological diagnosis of coeliac disease - a step forward.

Authors:  Geoffrey Holmes; Carolina Ciacci
Journal:  Gastroenterol Hepatol Bed Bench       Date:  2018

8.  A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method.

Authors:  Kazem Mashayekhi; Mohammad Rostami-Nejad; Davar Amani; Mostafa Rezaei-Tavirani; Hamid Mohaghegh-Shalmani; Mohammad Reza Zali
Journal:  Gastroenterol Hepatol Bed Bench       Date:  2018
  8 in total

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