Arthritis in Aboriginal Manitobans: evidence for a high burden of disease
Cheryl Barnabe1, Brenda Elias, Judith Bartlett
1Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Insights
Aboriginal Manitobans experience a higher burden of arthritis, with increased physician claims for rheumatoid arthritis and other arthropathies. Gaps in understanding their healthcare access patterns persist.
Area of Science:
- Public Health
- Rheumatology
- Epidemiology
Background:
- Arthritis significantly impacts populations globally, with varying prevalence and care patterns across diverse ethnic groups.
- Understanding the specific burden and healthcare experiences of Indigenous populations is crucial for equitable health outcomes.
Purpose of the Study:
- To assess the prevalence and patterns of arthritis care among Aboriginal Manitobans.
- To compare arthritis burden and healthcare utilization between First Nations individuals and other Manitobans.
Main Methods:
- Utilized three distinct data sources: physician claims (ICD-9 codes), the Manitoba First Nations Regional Longitudinal Health Survey (MFN Survey), and the Arthritis Centre research database.
- Compared data for First Nations (FN) Manitobans against all other Manitobans for physician claims and self-reported rates.
- Analyzed diagnostic patterns for Aboriginal versus Caucasian patients at the Arthritis Centre.
Main Results:
- First Nations Manitobans showed twice the rate of physician claims for rheumatoid arthritis, degenerative arthritis, and unspecified arthropathy compared to other Manitobans.
- The MFN Survey revealed a 21.0% self-reported arthritis rate and a 3.0% rheumatoid arthritis rate among First Nations individuals.
- Aboriginal patients at the Arthritis Centre were 2-4 times more likely to have inflammatory arthritis diagnoses and less likely to have non-inflammatory types.
Conclusions:
- The study confirms a greater burden of arthritis among Aboriginal Manitobans.
- Significant knowledge gaps exist regarding the reasons, timing, and methods of medical care access for Aboriginal individuals with arthritis.
Objective:
To evaluate the relative burden of arthritis and patterns of care in Aboriginal Manitobans, using multiple data sets to ensure a representative picture.
Methods:
Arthritis burden and healthcare utilization was ascertained using 3 separate data sources. Physician claims for 3 common ICD-9 musculoskeletal diagnoses were abstracted from the Population Health Research Data Repository for First Nations (FN) Manitobans and compared to all other Manitobans. Self-reported arthritis rates were obtained from the Manitoba First Nations Regional Longitudinal Health Survey (MFN Survey), which surveyed FN persons living on-reserve. Data on ethnicity and diagnoses were abstracted from the Arthritis Centre research database, which contains records of all patients seen at the Arthritis Centre.
Results:
Twice as many FN Manitobans had physician claims for rheumatoid arthritis, degenerative arthritis, and unspecified arthropathy compared to all other Manitobans. MFN Survey data identified a self-reported arthritis rate of 21.0% and a rheumatoid arthritis (RA) rate of 3.0%. Data for 687 Aboriginal patients and 4135 Caucasian patients were abstracted from the Arthritis Centre database. Aboriginal patients seen in the Arthritis Centre were 2 to 4 times more likely to have a diagnosis of inflammatory disease, and less than half as likely to have noninflammatory disease.
Conclusion:
The data highlight the increased burden of arthritis in Aboriginal Manitobans, and draw attention to large gaps in our knowledge of how, why, and when Aboriginals access medical care.
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