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Characterization of eosinophilic esophagitis variants by clinical, histological, and molecular analyses: A cross-sectional multi-center study.
Greuter, Thomas; Straumann, Alex; Fernandez-Marrero, Yuniel; Germic, Nina; Hosseini, Aref; Yousefi, Shida; Simon, Dagmar; Collins, Margaret H; Bussmann, Christian; Chehade, Mirna; Dellon, Evan S; Furuta, Glenn T; Gonsalves, Nirmala; Hirano, Ikuo; Moawad, Fouad J; Biedermann, Luc; Safroneeva, Ekaterina; Schoepfer, Alain M; Simon, Hans-Uwe.
Afiliação
  • Greuter T; Department of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland.
  • Straumann A; Division of Gastroenterology and Hepatology, University Hospital Lausanne - Centre Hopitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
  • Fernandez-Marrero Y; Department of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland.
  • Germic N; Institute of Pharmacology, University of Bern, Bern, Switzerland.
  • Hosseini A; Institute of Pharmacology, University of Bern, Bern, Switzerland.
  • Yousefi S; Institute of Pharmacology, University of Bern, Bern, Switzerland.
  • Simon D; Institute of Pharmacology, University of Bern, Bern, Switzerland.
  • Collins MH; Department of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Bussmann C; Division of Pathology, Cincinnati Children`s Hospital Medical Center, Cincinnati, Ohio, USA.
  • Chehade M; Pathology Viollier AG, Basel, Switzerland.
  • Dellon ES; Mount Sinai Center for Eosinophilic Disorders, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Furuta GT; Division of Gastroenterology and Hepatology, UNC Hospital, Chapel Hill, North Carolina, USA.
  • Gonsalves N; Department of Pediatrics, Gastrointestinal Eosinophilic Diseases Program, Digestive Health Institute, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Hirano I; Division of Gastroenterology and Hepatology, Northwestern University, Chicago, Illinois, USA.
  • Moawad FJ; Division of Gastroenterology and Hepatology, Northwestern University, Chicago, Illinois, USA.
  • Biedermann L; Division of Gastroenterology, Scripps Clinic, La Jolla, California, USA.
  • Safroneeva E; Department of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland.
  • Schoepfer AM; Insitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Simon HU; Division of Gastroenterology and Hepatology, University Hospital Lausanne - Centre Hopitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Allergy ; 77(8): 2520-2533, 2022 08.
Article em En | MEDLINE | ID: mdl-35094416
OBJECTIVE: Physicians are increasingly confronted with patients presenting with symptoms of esophageal dysfunction resembling eosinophilic esophagitis (EoE), but absence of significant esophageal eosinophilia. The purpose of this study was to characterize and classify this group of EoE variants. DESIGN: Patients from six EoE-centers with symptoms of esophageal dysfunction, but peak eosinophil counts of <60/mm2 (<15/hpf) in esophageal biopsies and absence of gastro-esophageal reflux disease (GERD) were included. Clinical, endoscopic, (immuno)-histological, and molecular features were determined and compared with EoE, GERD, and healthy controls. RESULTS: We included 69 patients with EoE variants. Endoscopic abnormalities were found in 53.6%. We identified three histological subtypes: EoE-like esophagitis (36/69, 52.2%), lymphocytic esophagitis (14/69, 20.3%), and non-specific esophagitis (19/69, 27.5%). Immunohistochemistry revealed-in contrast to EoE-no significant increase in inflammatory cell infiltrates compared with GERD and healthy controls, except for lymphocytes in lymphocytic esophagitis. EoE-typical Th2-response was absent in all EoE variants. However, considerable structural changes were detected based on histology and protein expression. Using next generation mRNA sequencing, we found the three EoE variants to have distinct molecular fingerprints partially sharing pronounced traits of EoE. Hierarchical sample clustering of RNA sequencing data confirmed the presence of an EoE-like (characterized by eotaxin-3 expression), non-specific, and lymphocytic variant cluster (characterized by CD3 cells and TSLP expression). CONCLUSION: All EoE variants are clinically and histologically active conditions despite the absence of esophageal eosinophilia. EoE variants appear to be part of a disease spectrum, where classical EoE represents the most common and apparent phenotype.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Refluxo Gastroesofágico / Esofagite Eosinofílica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Refluxo Gastroesofágico / Esofagite Eosinofílica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article