Collagenous gastritis: Epidemiology and clinical associations.

Autoimmune gastritis Celiac disease Collagenous gastritis Duodenal intraepithelial lymphocytosis Environmental risk factors Epidemiology Helicobacter pylori Microscopic colitis

Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 19 02 2021
revised: 04 03 2021
accepted: 10 03 2021
pubmed: 8 4 2021
medline: 4 2 2022
entrez: 7 4 2021
Statut: ppublish

Résumé

the rare occurrence of collagenous gastritis (CG) makes its epidemiology difficult to investigate. We designed a study to determine the demographic and clinical characteristics as well as the associations of CG with other upper gastrointestinal diseases in a large national clinicopathological database. from the IDEA database we extracted all patients with histopathologically documented CG and, in a case-control study, we compared 168 subjects with and 1,286,165 subjects without CG using odds ratios (OR) with their 95% confidence intervals (CI). the prevalence of CG was 13 per 100,000 EGDs. CG was significantly more common among female than male patients (OR: 1.69, 95% CI: 1.20-2.39) and was characterized by a bi-modal age distribution (first peak in patients aged 10-19, second peak primarily in females aged >60 years). CG patients presented with diarrhea (18%), anemia (12%), weight loss (11%), and vomiting (10%). CG was significantly associated with other lymphocytic disorders of the upper gastrointestinal tract, including celiac sprue (2.12, 1.55-2.88), duodenal intraepithelial lymphocytosis (3.71, 2.30-5.98), and lymphocytic gastritis (23.2, 10.9-49.5). CG persisted in 69% of patients who underwent multiple consecutive endoscopies. the epidemiologic features of collagenous gastritis reflect on different etiologies contributing to its occurrence in children and adults.

Sections du résumé

BACKGROUND BACKGROUND
the rare occurrence of collagenous gastritis (CG) makes its epidemiology difficult to investigate. We designed a study to determine the demographic and clinical characteristics as well as the associations of CG with other upper gastrointestinal diseases in a large national clinicopathological database.
METHODS METHODS
from the IDEA database we extracted all patients with histopathologically documented CG and, in a case-control study, we compared 168 subjects with and 1,286,165 subjects without CG using odds ratios (OR) with their 95% confidence intervals (CI).
RESULTS RESULTS
the prevalence of CG was 13 per 100,000 EGDs. CG was significantly more common among female than male patients (OR: 1.69, 95% CI: 1.20-2.39) and was characterized by a bi-modal age distribution (first peak in patients aged 10-19, second peak primarily in females aged >60 years). CG patients presented with diarrhea (18%), anemia (12%), weight loss (11%), and vomiting (10%). CG was significantly associated with other lymphocytic disorders of the upper gastrointestinal tract, including celiac sprue (2.12, 1.55-2.88), duodenal intraepithelial lymphocytosis (3.71, 2.30-5.98), and lymphocytic gastritis (23.2, 10.9-49.5). CG persisted in 69% of patients who underwent multiple consecutive endoscopies.
CONCLUSIONS CONCLUSIONS
the epidemiologic features of collagenous gastritis reflect on different etiologies contributing to its occurrence in children and adults.

Identifiants

pubmed: 33824091
pii: S1590-8658(21)00124-9
doi: 10.1016/j.dld.2021.03.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1136-1140

Informations de copyright

Copyright © 2021 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest RM Genta, KO Turner, and CJ Morgan are employed by Inform Diagnostics, Irving, TX. A Sonnenberg has no conflict of interest to declare. No funding was obtained for this study. Author Contributions: Study conception and design: A Sonnenberg, RM Genta; data analysis: A Sonnenberg, RM Genta, KO Turner; review of biopsy specimens and photographs: CJ Morgan; writing of manuscript: RM Genta, A Sonnenberg.

Auteurs

Robert M Genta (RM)

Inform Diagnostics, Irving, TX, United States; Baylor College of Medicine, Houston, TX, United States. Electronic address: rmgenta@gastropath.com.

Kevin O Turner (KO)

Inform Diagnostics, Irving, TX, United States.

Christopher J Morgan (CJ)

Inform Diagnostics, Irving, TX, United States.

Amnon Sonnenberg (A)

Division of Gastroenterology, Portland VA Medical Center and Oregon Health and Science University, United States.

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Classifications MeSH