Retrospective Review of Pediatric and Adult Autoimmune Hepatitis in Two Quaternary Care Centres in British Columbia: Increased Prevalence Seen in British Columbia’S First Nations Community

Author:

Chung Henry V1,Riley Mark2,Ho Jin K1,Leung Benjamin3,Jevon Gareth P4,Arbour Laura T5,Barker Colin2,Schreiber Richard2,Yoshida Eric M16

Affiliation:

1. Division of Gastroenterology, Department of Medicine, University of British Columbia, Canada

2. Department of Pediatrics, University of British Columbia, Canada

3. Department of Medicine, University of British Columbia, Canada

4. Department of Pathology, University of British Columbia, Canada

5. Department of Medical Genetics, University of British Columbia, Canada

6. British Columbia Transplant Society, Vancouver, British Columbia, Canada

Abstract

BACKGROUND: It has been previously reported that British Columbia’s (BC’s) First Nations (Aboriginal) community has an increased risk of autoimmune diseases, including rheumatological conditions (rheumatoid arthritis, systemic lupus) and primary biliary cirrhosis. The researchers hypothesized that this community may also be at increased risk for autoimmune hepatitis (AIH).METHODS: Independent, retrospective reviews of the databases of two separate tertiary/quaternary British Columbia university-affiliated health care institutions, the Adult Liver Transplant Program of the BC Transplant Society and the Division of Pediatric Gastroenterology, BC Children’s Hospital (Vancouver, BC), were performed. All patients referred with a diagnosis of probable or definite AIH who identified themselves as being of First Nations descent from 1988 to 2004 were reviewed. The liver transplant database records all adult patients in the province referred for transplant assessment. The pediatric database records all children referred to the BC Children’s Hospital.RESULTS: A total of 68 adult patients with a definite or probable diagnosis of AIH were referred to the liver transplant program. Twelve patients (17.6%) were Aboriginal, 11 of which were female. Similarly, a total of 30 children with probable or definite AIH were identified from the pediatric database. Six of these cases (20%) were identified in Aboriginal children.CONCLUSIONS: The findings suggest an increased prevalence of AIH among BC’s First Nations community. A disproportionate First Nations representation was found on independent review of two databases. Future studies are needed to determine the true prevalence of AIH in this community, and to uncover the genetic predisposition and the environmental triggers explaining this phenomenon.

Publisher

Hindawi Limited

Subject

Gastroenterology,General Medicine

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