1. Ultra-short celiac disease exhibits differential genetic and immunophenotypic features compared to conventional celiac disease
- Author
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Pilar Mata-Romero, Daniel Martín-Holgado, Hal C. Ferreira-Nossa, Pedro L. González-Cordero, Ana Izquierdo-Martín, Patricia Barros-García, Nuria Fernandez-Gonzalez, Luis Fernández-Pereira, Carmen Cámara-Hijón, and Javier Molina-Infante
- Subjects
Adult ,Transglutaminases ,Hepatology ,Duodenum ,Biopsy ,Gastroenterology ,Immunoglobulin A ,Celiac Disease ,GTP-Binding Proteins ,Humans ,Protein Glutamine gamma Glutamyltransferase 2 ,Prospective Studies ,Child ,Autoantibodies - Abstract
Ultra-short coeliac disease (USCD) is a novel celiac disease (CD) subtype limited to the duodenal bulb (D1). HLA haplotypes and flow cytometry have not been assessed yet.To compare genetic, clinical, serologic, histopathologic and inmmunophenotypic parameters between USCD and conventional celiac disease (CCD) patients.Prospective single-center study in children and adult patients undergoing duodenal biopsies on a gluten-containing diet. Biopsies for histology and flow cytometry were taken separately from D1 and distal duodenum. Biopsies in seronegative patients with celiac lymphogram were repeated after 2 years on a gluten-free diet.Among 505 included patients, 127 were diagnosed with CD, of whom 7 (5.5%) showed USCD. HLADQ2 was significantly less common in USCD compared to CCD (71% vs. 95%, p 0.003). Likewise, USCD patients showed more frequent non-significant seronegativity (28% vs. 8%, p 0.07) and significantly lower titrations (7-15IU/ml) of tissue transglutaminase antibodies (tTG-IgA) (60% vs. 13%, p0.001). Biopsies from D1 revealed significant less NK cells down-expression in USCD patients (1.4 vs. 5, p 0.04).Up to 5.5% of CD patients showed USCD. A lower frequency of HLADQ2, along with less serum tTG-IgA titration and duodenal NK cell suppression, were differential features of USCD.
- Published
- 2021