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Scand J Gastroenterol ; 54(5): 563-570, 2019 May.
Article in English | MEDLINE | ID: mdl-31057009

ABSTRACT

Background: Seronegative celiac disease (CD) poses a diagnostic challenge. Aims: Characterize and identify differences between seronegative and seropositive CD. Patients and methods: Retrospective cohort study examining adult patients diagnosed with CD (1980-2017). Clinical, analytical, histological, genetic and immunophenotypic data were compiled. Seronegative CD was defined as a anti-tissue transglutaminase type 2 IgA and endomysial antibodies (EMA) negative and HLA-DQ2 and/or DQ8 positive, showing clinical signs of CD plus an abnormal duodenal biopsy, and responding to a gluten-free diet (GFD). Factors associated with seronegative CD were identified through binomial logistic regression. Results: Of 315 CD patients, 289 were seropositive (91.7%) and 26 seronegative (8.3%). Among the seronegative patients, higher prevalence was observed for autoimmune thyroiditis (26.9% vs. 9.7%, p = .016), HLA-DQ8 heterozygosity (23.1% vs. 2.5%, p ˂ .001) and Marsh I lesion (34.6% vs. 3.7%, p ˂ .001). The two groups showed similar flow cytometry-determined duodenal immunophenotypes and rates of refractory CD. Conclusions: Seronegative CD differs mostly in genetic (more HLA-DQ8) and histologic (milder atrophy) features as compared with seropositive. Intestinal intraepithelial immunophenotype by flow cytometry, similar in both modalities, is a useful tool to diagnose seronegative CD.


Subject(s)
Celiac Disease/genetics , Celiac Disease/pathology , Duodenum/pathology , Lymphocytes/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Atrophy , Autoantibodies/blood , Biopsy , Celiac Disease/diagnosis , Celiac Disease/diet therapy , Diet, Gluten-Free , Duodenal Diseases/diagnosis , Duodenal Diseases/genetics , Duodenal Diseases/pathology , Female , Flow Cytometry , GTP-Binding Proteins/blood , HLA-DQ Antigens/genetics , Humans , Immunoglobulin A/immunology , Intestinal Mucosa/pathology , Logistic Models , Male , Middle Aged , Protein Glutamine gamma Glutamyltransferase 2 , Retrospective Studies , Transglutaminases/blood , Young Adult
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