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Published on: February 14, 2021
Inflammatory Bowel Disease in Indigenous Populations: A Scoping Review
Omer Munir1, Cass Condray2,3, Adrielle Souza Lira1
1College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
Inflammatory bowel disease (IBD) research in Indigenous populations is limited, though rates may be rising. Future studies must include Indigenous peoples as research partners and utilize Indigenous research methodologies to improve inclusivity and understanding.
Area of Science:
- Gastroenterology
- Public Health
- Health Equity
Background:
- Global inflammatory bowel disease (IBD) incidence is increasing.
- Indigenous populations are underrepresented in IBD research.
- Socioeconomic factors present unique healthcare challenges for Indigenous peoples.
Purpose of the Study:
- To synthesize existing literature on IBD in global Indigenous populations.
- To identify critical research gaps concerning IBD in these communities.
- To propose recommendations for enhancing research inclusivity.
Main Methods:
- Comprehensive literature search across 8 databases (e.g., MEDLINE, EMBASE).
- Inclusion of diverse study types (qualitative, quantitative, mixed-methods, commentaries).
- Critical appraisal and synthesis of 18 selected publications since 1962.
Main Results:
- Limited research originates primarily from Canada, New Zealand, and Australia.
- Indigenous populations generally show lower IBD rates, but recent increases are noted.
- Barriers to healthcare access and minimal Indigenous engagement in research were identified.
Conclusions:
- Significant gaps exist in understanding IBD among Indigenous populations.
- Rising IBD rates in Indigenous communities warrant further investigation into genetic and environmental factors.
- Inclusion of Indigenous peoples as research partners and adherence to Indigenous research methodologies are crucial.
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