Autoimmune atrophic gastritis and coeliac disease: A case-control study.


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:
01 2023
Historique:
received: 06 04 2022
revised: 30 06 2022
accepted: 01 07 2022
pubmed: 30 7 2022
medline: 31 12 2022
entrez: 29 7 2022
Statut: ppublish

Résumé

Autoimmune atrophic gastritis (AAG) is rarely associated with coeliac disease (CD). To assess the frequency of AAG-CD association and to compare clinical, biochemical, and histological features of adults affected by both diseases (cases) with AAG controls. This case-control study included 9 cases (F55%, median age 47, range 23-59yrs) matched (1:3) by age (±4 yrs) and gender to 27 controls randomly selected from our AAG cohort (2009-2021). The AAG and CD diagnosis was based on internationally agreed criteria. Of 434 AAG patients (median age:62.5yrs, range18-92yrs, F:M ratio=2.2:1),9 had a concomitant diagnosis of CD. The occurrence of AAG-CD association was 2% and 1.65% among AAG/CD cohorts, respectively. Cases were significantly younger than AAG cohort (n = 425, p = 0.002). In 4/9cases, AAG was diagnosed by proactive screening for autoimmune disorders. Autoimmune thyroid disorders were present in 5/9 cases. Cases had a significant higher prevalence of normocytic anaemia than controls (p = 0.004). No significant differences were found between cases and controls concerning clinical and histological features. AAG-CD association is rare. Gastric and duodenal biopsies might be advisable in young people with normocytic anaemia and associated autoimmune disorders to timely diagnose clinically silent conditions.

Sections du résumé

BACKGROUND
Autoimmune atrophic gastritis (AAG) is rarely associated with coeliac disease (CD).
AIMS
To assess the frequency of AAG-CD association and to compare clinical, biochemical, and histological features of adults affected by both diseases (cases) with AAG controls.
METHODS
This case-control study included 9 cases (F55%, median age 47, range 23-59yrs) matched (1:3) by age (±4 yrs) and gender to 27 controls randomly selected from our AAG cohort (2009-2021). The AAG and CD diagnosis was based on internationally agreed criteria.
RESULTS
Of 434 AAG patients (median age:62.5yrs, range18-92yrs, F:M ratio=2.2:1),9 had a concomitant diagnosis of CD. The occurrence of AAG-CD association was 2% and 1.65% among AAG/CD cohorts, respectively. Cases were significantly younger than AAG cohort (n = 425, p = 0.002). In 4/9cases, AAG was diagnosed by proactive screening for autoimmune disorders. Autoimmune thyroid disorders were present in 5/9 cases. Cases had a significant higher prevalence of normocytic anaemia than controls (p = 0.004). No significant differences were found between cases and controls concerning clinical and histological features.
CONCLUSIONS
AAG-CD association is rare. Gastric and duodenal biopsies might be advisable in young people with normocytic anaemia and associated autoimmune disorders to timely diagnose clinically silent conditions.

Identifiants

pubmed: 35906165
pii: S1590-8658(22)00583-7
doi: 10.1016/j.dld.2022.07.001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-74

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflict of interest.

Auteurs

Laura Conti (L)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy. Electronic address: l.conti@uniroma1.it.

Gloria Galli (G)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy.

Chiara Ligato (C)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy.

Marilia Carabotti (M)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy.

Bruno Annibale (B)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy.

Edith Lahner (E)

Medical-Surgical Department of Clinical Sciences and Translational Medicine, Sapienza Affiliations: University of Rome, Italy.

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Classifications MeSH