Osteoporosis management and fractures in the Métis of Ontario, Canada.

UNLABELLED: Half of Métis citizens, compared to less than 10 % of the general population of Ontario, reside in northern regions, with little access to bone mineral density (BMD) testing. Métis citizens had lower sex-specific and age-standardized rates of BMD testing, yet similar rates of fracture (both sexes) and pharmacotherapy (women only).
PURPOSE: To examine osteoporosis management and common osteoporosis-related fractures among Métis citizens compared to the general population of older adults residing in Ontario.
METHODS: We linked healthcare (medical and pharmacy) utilization and administrative (demographic) databases with the Métis Nation of Ontario citizenship registry to estimate osteoporosis management (bone mineral density [BMD] testing, pharmacotherapy) and fractures (hip, humerus, radius/ulna) among adults aged ≥50 years, from April 1, 2006 to March 31, 2011. Pharmacotherapy data were limited to residents aged ≥65 years. Sex-specific and age-standardized rates were compared between the Métis and the general population. Multivariable logistic regression was used to compare rates of BMD testing after controlling for differences in age and region of residence between the Métis and the general population.
RESULTS: We studied 4219 Métis citizens (55 % men), and 140 (3 %) experienced a fracture. Half of Métis citizens, compared to less than 10 % of the general population of Ontario, resided in northern regions. We identified significantly lower sex-specific and age-standardized rates of BMD testing among Métis compared to the general population, yet found little difference in fracture rates (both sexes) or pharmacotherapy (women only). Differences in BMD testing disappeared after adjusting for region of residence among women yet remained significant among men.
CONCLUSIONS: Despite finding significantly lower rates of osteoporosis management among men, Métis men and women were found to have similar age-standardized fracture rates to the general population.

Introduction

The Canadian Constitution recognizes three groups of Aboriginal peoples: First Nations, Inuit, and Métis [1]. First Nations people are those who identify as North American Indians and are descendants of the original inhabitants of Canada [2]. The Inuit are Aboriginal peoples who mostly inhabit Nunatsiavut (northern coastal Labrador), Nunavik (northern Québec), the territory of Nunavut, and the Inuvialuit region of the Northwest Territories [3]. The Métis are descendants of unions between European men and First Nations women during the early 17th century to late 19th century [4-6], developing a culture, history, and lifestyle distinct from First Nations and Inuit people [5]. In 2011, 451,795 people identified as Métis in Canada, representing 32 % of the total Aboriginal population [3]. Despite their significant numbers, Métis are either not identified specifically or are underrepresented in Aboriginal health research [3, 5, 7, 8]. Most research has focused on First Nations; however, the Métis may differ in their health behaviours and prevalence of risk factors and disease and may require specific health interventions unique to their culture. In addition, the Métis receive significantly fewer local, provincial, and national resources for healthcare in comparison to First Nations and Inuit [9].

About one fifth (86,015 or 19 %) of all Métis reside in Ontario, constituting the second largest provincial Métis population in Canada [3]. The Métis Nation of Ontario was established in 1993 to address the needs of this large population, and it continues to serve as the principal voice for the Métis people in the province. One key contribution of the Métis Nation of Ontario has involved establishing a voluntary registry of Métis citizens residing in Ontario [10]. Data collected and maintained by the Métis Nation of Ontario within the provincial registry has permitted a closer examination of key health challenges facing Métis people in Ontario.

In 2010, the Métis Nation of Ontario entered into a partnership with the Public Health Agency of Canada and the Institute for Clinical Evaluative Sciences to examine rates of selected chronic diseases among Métis. Results have identified higher rates of cardiovascular disease [11], diabetes [12], and chronic obstructive pulmonary disease [13] among Métis compared to the general population of Ontario. The purpose of our study was to compare rates of osteoporosis management and fractures among Métis to the general population in Ontario.

Methods

Residents of all ages in Ontario have access to publicly funded medical care and become eligible to receive pharmacy benefits at the age of 65 years. We linked healthcare (medical and pharmacy) utilization and administrative (demographic) databases from the Ontario Ministry of Health and Long-Term Care, housed at the Institute for Clinical Evaluative Sciences, to the Métis Nation of Ontario citizenship registry to compare osteoporosis management and fracture rates between Métis citizens and the general population.

Adults aged 50 or more years as of April 1, 2006 were eligible. Ontario residents not registered with the Métis Nation of Ontario were considered part of the general population. We excluded individuals residing in long-term care or whose last date of contact with the healthcare system was before April 1, 2001. We therefore focused on community-dwelling residents with some healthcare services utilization within the past 5 years. Age, sex, neighbourhood income, region of residence, and urban status were determined as of April 1, 2006. Neighbourhood income was based on census data and categorized into quintiles ranked from poorest to wealthiest. Region of residence was categorized into four main areas based on the number of densitometers (bone mineral density [BMD] machines) [14, 15] and sample size of Métis in each of the province’s local health integration networks: 1. Southwestern (moderate access to densitometry), 2. Southcentral (high density of densitometers and bone specialists, e.g. Hamilton and Toronto), 3. Southeastern (moderate access to densitometry), and 4. Northern (few densitometers).

Urban residence was based on postal code and defined according to the standard geographical classification definition outlined by Statistics Canada: urban areas have a population of at least 1000 and a population density of at least 400 persons per square kilometre [16]. Fracture history (any of hip, humerus, or radius/ulna) within 6 months prior to April 1, 2006 and osteoporosis management (BMD testing and osteoporosis pharmacotherapy) within 1 year prior to April 1, 2006 were also summarized.

Osteoporosis pharmacotherapy was examined among residents aged 65 years or more and included bisphosphonates, calcitonin, denosumab, and raloxifene. Teriparatide is not covered by the provincial drug plan [17, 18] and thus was not considered.

Our main outcomes were 5-year rates of osteoporosis management (BMD testing and pharmacotherapy [19]) and fracture (hip, humerus, radius/ulna, or any of these). Given the known differences in osteoporosis fracture rates by sex [20] and prior evidence of an inverted U-shape between age and rates of BMD testing (rates peak among those aged 60–69 years and are lower among those aged younger than 60 and older than 69 years [14, 21]), results were stratified by sex and age group.

Crude and age-standardized rates were reported per 10,000 persons. Age-standardized rates were calculated using four age groups (50–64, 65–70, 70–74, and ≥75 years of age), by direct standardization according to the 1991 Ontario census population with gamma distribution to estimate 95 % confidence intervals. The direct standardization method permits the direct comparison of rates between the Métis and the general population since rates in both groups are standardized according to the age distribution of the same referent (standard) population [22]. Logistic regression was then used to examine if Métis status was independently associated with BMD testing after adjusting for age, income, region of residence, and urban status. Given that neighbourhood income, region of residence, and urban status are all based on postal code data, we also examined potential collinearity between the different possible combinations of variables using chi-square contingency tables.

Results

We identified 4219 eligible Métis citizens and 3,822,661 eligible persons from the general population of Ontario (Fig. 1). Métis citizens were younger, had lower income status, and fewer lived in urban areas (Table 1). Almost half of Métis citizens, compared to less than 10 % of the general population of Ontario, resided in northern regions, with little to no access to BMD testing.

Fig. 1

Study flow diagram of the Métis and the general population inclusion. Missing data refers to missing information regarding neighbourhood income, region of residence, and “urban” status

Table 1

Characteristics of the Métis and the general population, 1 April 2006

Characteristic	Men		Women
	Métis	General	Métis	General
	N = 2321	N = 1,804,959	N = 1898	N = 2,017,702
Median age, years (IQR)	59 (53–66)	61 (55–70)	59 (54–67)	62 (55–72)
Mean age, years (SD)	60.2 (8.2)	63.0 (10.0)	60.8 (8.7)	64.4 (10.9)
Age in years (%)
50–54	30.9	24.3	30.5	22.3
55–59	23.6	21.5	21.7	19.8
60–64	17.3	15.8	17.5	14.7
65–69	13.2	12.4	12.5	12.0
70–74	8.7	10.3	9.1	10.5
≥75	6.3	15.7	8.6	20.7
Neighbourhood income quintile (%)a
1 (lowest income)	23.5	18.1	23.5	19.3
2	20.7	19.9	21.6	20.4
3	21.4	19.5	19.3	19.4
4	17.7	20.4	18.8	19.8
5 (highest income)	16.7	22.2	16.8	21.1
Region of residence (%)a
Southwestern	7.1	18.3	7.9	18.3
Erie St. Clair	2.4	5.4	2.1	5.3
South West	3.5	7.8	3.6	7.9
Waterloo Wellington	1.2	5.1	2.2	5.1
Southcentral	9.2	44.7	13.5	45.0
Hamilton Niagara Haldimand Brant	4.0	11.6	6.9	11.8
Central West	0.9	5.0	1.0	4.8
Mississauga Halton	1.1	7.6	1.9	7.5
Toronto Central	1.5	8.5	1.8	8.8
Central	1.7	11.9	2.0	12.1
Southeastern	33.0	29.5	34.6	29.6
Central East	4.7	11.8	4.6	11.9
South East	3.6	4.5	2.4	4.5
Champlain	4.5	9.5	4.8	9.6
North Simcoe Muskoka	20.3	3.7	22.8	3.6
Northern	50.6	7.5	44.0	7.1
North East	36.1	5.4	29.4	5.2
North West	14.5	2.1	14.6	1.9
Urban residence (%)a	62.4	85.5	68.3	86.6
Fracture historyb	0.1	0.3	0.7	0.6
Osteoporosis managementc
Bone mineral density test	1.5	2.5	16.4	19.5
Pharmacotherapy (aged ≥65)d	1.7	4.1	22.6	26.3

aProportions adjusted for missing data for neighbourhood income (1 % Métis and 0.7 % general population) and region (0.5 % Métis and 0.4 % general population)

bHip, humerus, or radius/ulna fracture within 6 months prior to April 1, 2006

c1 year lookback from April 1, 2006 (April 1, 2005 to March 31, 2006)

dOsteoporosis pharmacotherapy includes bisphosphonates, calcitonin, denosumab, and raloxifene

Osteoporosis management

The proportion of Ontario residents receiving BMD testing was substantially lower among men (11 %) than among women (55 %). Although patterns of BMD testing were similar by age group among persons of the same sex (Fig. 2), fewer Métis citizens were tested after standardizing for age, Table 2. Differences in BMD testing disappeared after adjusting for neighbourhood income and region of residence among women, yet remained significant among men, Table 3. Métis men also had lower rates of osteoporosis pharmacotherapy, even after adjusting for age. In contrast, rates of osteoporosis pharmacotherapy were similar among Métis women and the general population.

Fig. 2

Five-year bone mineral density (BMD) testing rates among the Métis (closed circle) and the general population (open square), by age group, stratified by sex. 95 % confidence intervals for Métis estimates are wide and overlap with the general population in all comparisons

Table 2

Five-year ratesa of osteoporosis management and fractures in the Métis and the general population of Ontario

Outcome of interest	Men		Women
	Métis	General population	Métis	General population
	N = 2321	N = 180,959	N = 1898	N = 2,017,702
Osteoporosis management
1. Bone mineral density test
N	136	197,730	923	1,102,997
Crude rate (95 % CI)	122.4 (102.8–144.7)	230.1 (229.1–231.1)	999.1 (935.7–1065.7)	1137.1 (1134.9–1139.2)
Age-standardized rate (95 % CI)	134.2 (110.9–160.9)	245.5 (244.4–246.6)*	969.1 (889.3–1054.1)	1135.1 (1132.9–1137.3)*
2. Osteoporosis pharmacotherapy (aged ≥65)b
N	35	63,205	203	345,213
Crude rate (95 % CI)	114.1 (79.5–158.6)	201.4 (199.8–203.0)	751.2 (651.4–861.9)	855.7 (852.8–858.5)
Age-standardized rate (95 % CI)	125.5 (82.8–182.4)	198.7 (197.0–200.4)*	758.4 (626.3–910.1)	850.9 (847.9–854.0)
3. Osteoporosis management (BMD test or pharmacotherapy)b
N	150	219,668	993	1,201,199
Crude rate (95 % CI)	134.9 (114.2–158.2)	255.6 (254.5–256.7)	1074.9 (1009.1–1143.9)	1238.4 (1236.2–1240.6)
Age-standardized rate (95 % CI)	161.3 (133.4–193.2)	274.6 (273.4–275.8)*	1093.2 (1007.6–1184.0)	1254.3 (1251.9–1256.6)*
Fractures
1. Hip fracture
N	16	14,670	14	34,675
Crude rate (95 % CI)	14.3 (8.2–23.2)	17.1 (16.8–17.4)	15.2 (8.3–25.4)	35.7 (35.4–36.1)
Age-standardized rate (95 % CI)	24.7 (11.7–46.0)	18.8 (18.4–19.1)	26.7 (13.3–47.9)	41.1 (40.5–41.6)
2. Humerus fracture
N	12	11,278	22	30,070
Crude rate (95 % CI)	10.7 (5.5–18.7)	13.1 (12.9–13.4)	23.8 (14.9–36.1)	31.0 (30.7–31.4)
Age-standardized rate (95 % CI)	13.5 (5.9–26.3)	13.7 (13.4–14.0)	25.2 (14.9–40.0)	33.4 (33.0–33.9)
3. Radius or ulna fracture
N	21	20,452	65	63,796
Crude rate (95 % CI)	18.8 (11.6–28.7)	23.8 (23.5–24.1)	70.4 (54.3–89.7)	65.8 (65.3–66.3)
Age-standardized rate (95 % CI)	19.2 (11.2–30.7)	24.1 (23.7–24.4)	77.8 (57.6–102.7)	68.2 (67.6–68.7)
4. Any fracture (hip, humerus, radius/ulna)
N	45	43,132	95	116,539
Crude rate (95 % CI)	40.2 (29.3–53.8)	50.2 (49.7–50.7)	102.8 (83.2–125.7)	120.1 (119.4–120.8)
Age-standardized rate (95 % CI)	53.8 (35.8–77.8)	52.5 (52.0–53.1)	122.5 (95.8–154.4)	128.9 (128.1–129.8)

*Differences in age-standardized rates are statistically significant, p < 0.05

aRates per 10,000 people; age-standardized using sex-specific direct standardization to the 1991 Canadian population

bOsteoporosis pharmacotherapy includes bisphosphonates, calcitonin, denosumab, and raloxifene

Table 3

Odds ratio estimates for bone mineral density (BMD) testing among Métis vs. general population of Ontario by sex; unadjusted and adjusted for age, income, and region of residence

Characteristic	Men		Women
	Unadjusted	Adjusted	Unadjusted	Adjusted
	OR (95 % CI)	OR (95 % CI)	OR (95 % CI)	OR (95 % CI)
	N = 1,793,883	N = 1,793,883	N = 2,006,619	N = 2,006,619
Métis citizen	0.51 (0.43–0.61)	0.82 (0.69–0.98)	0.78 (0.71–0.86)	0.95 (0.87–1.04)
Age in years
50–54	1	1	1	1
55–59	1.60 (1.57–1.63)	1.61 (1.58–1.64)	1.31 (1.30–1.33)	1.33 (1.32–1.34)
60–64	2.97 (2.91–3.02)	3.03 (2.98–3.08)	1.53 (1.51–1.54)	1.57 (1.56–1.59)
65–69	4.15 (4.08–4.23)	4.26 (4.19–4.34)	1.43 (1.42–1.44)	1.48 (1.46–1.50)
70–74	4.56 (4.48–4.65)	4.69 (4.60–4.77)	1.12 (1.11–1.13)	1.16 (1.15–1.17)
≥75	3.84 (3.77–3.91)	3.91 (3.84–3.98)	0.50 (0.49–0.50)	0.51 (0.50–0.51)
Neighbourhood income quintile
1 (lowest income)	1	1	1	1
2	1.05 (1.04–1.07)	1.03 (1.02–1.05)	1.17 (1.16–1.18)	1.14 (1.13–1.15)
3	1.04 (1.02–1.06)	1.05 (1.03–1.06)	1.27 (1.26–1.28)	1.23 (1.22–1.24)
4	1.06 (1.04–1.07)	1.06 (1.04–1.07)	1.41 (1.39–1.42)	1.32 (1.31–1.33)
5 (highest income)	1.11 (1.10–1.13)	1.10 (1.09–1.12)	1.58 (1.57–1.60)	1.47 (1.46–1.49)
Region of residence
Southwesterna
Erie St. Clair	1	1	1	1
South West	1.30 (1.26–1.35)	1.36 (1.32–1.41)	1.07 (1.06–1.09)	1.11 (1.09–1.12)
Waterloo Wellington	1.72 (1.66–1.78)	1.79 (1.73–1.85)	1.52 (1.49–1.54)	1.53 (1.50–1.55)
Southcentrala
Hamilton Niagara Haldimand Brant	2.31 (2.24–2.38)	2.29 (2.23–2.36)	1.80 (1.77–1.82)	1.85 (1.82–1.88)
Central West	1.93 (1.87–2.00)	2.04 (1.97–2.11)	1.78 (1.75–1.81)	1.73 (1.70–1.76)
Mississauga Halton	2.08 (2.02–2.15)	2.17 (2.11–2.24)	2.30 (2.27–2.34)	2.19 (2.16–2.23)
Toronto Central	2.43 (2.36–2.51)	2.51 (2.43–2.59)	1.87 (1.84–1.90)	1.91 (1.88–1.94)
Central	2.66 (2.58–2.73)	2.71 (2.63–2.79)	2.21 (2.17–2.34)	2.18 (2.15–2.22)
Southeasterna
Central East	2.16 (2.10–2.23)	2.23 (2.16–2.29)	1.75 (1.73–1.78)	1.81 (1.78–1.84)
South East	1.49 (1.44–1.55)	1.54 (1.49–1.60)	1.17 (1.15–1.19)	1.23 (1.21–1.25)
Champlain	1.65 (1.60–1.70)	1.73 (1.68–1.78)	1.62 (1.60–1.65)	1.63 (1.61–1.66)
North Simcoe Muskoka	1.46 (1.41–1.52)	1.52 (1.46–1.58)	1.56 (1.53–1.59)	1.61 (1.57–1.64)
Northerna
North East	1.17 (1.13–1.22)	1.22 (1.18–1.26)	0.93 (0.91–0.95)	0.95 (0.93–0.97)
North West	0.58 (0.55–0.62)	0.62 (0.58–0.66)	0.72 (0.71–0.74)	0.73 (0.71–0.75)
Urban residence	1.51 (1.49–1.53)	1.18 (1.16–1.20)	1.41 (1.40–1.42)	1.11 (1.10–1.12)

aRegion of residence was categorized into four main areas based on the number of densitometers (BMD machines) [14, 15] and sample size of Métis in each of the province’s local health integration networks: Southwestern (moderate access to densitometry), Southcentral (high density of densitometers and bone specialists, e.g. Hamilton and Toronto), Southeastern (moderate access to densitometry), and Northern (few densitometers)

Fracture rates

As expected, fracture rates increased with increasing age in both sexes (Fig. 3) and were higher among women (from 2.9 % aged 50–54 to 12.0 % aged 75 and older) than among men (from 1.5 % aged 50–54 to 5.4 % aged 75 and older). Crude rates of hip fracture were significantly lower among Métis women (15.2 per 10,000 persons, 95 % CI = 8.3–25.4) compared to women in the general population (35.7 per 10,000 persons, 95 % CI = 35.4–36.1), yet this difference disappeared after standardizing for age (Table 2). Similarly, we identified little difference in all sex-specific fracture rates between Métis citizens and the general population after standardizing for age.

Fig. 3

Five-year fracture rates among the Métis (closed circle) and the general population (open square), by age group, stratified by sex. Any fracture refers to a fracture of the hip, humerus, or radius/ulna. The 95 % confidence intervals for Métis estimates are wide and overlap with the general population in all comparisons

Discussion

We identified significantly lower sex-specific and age-standardized rates of BMD testing among Métis compared to the general population, yet found little difference in fracture rates (both sexes) or pharmacotherapy (women only). Differences in BMD testing disappeared after adjusting for region of residence among women, yet remained significant among men.

Prior research identifies regional differences in BMD testing for osteoporosis based on access to BMD testing sites [23], which are largely located in urban centres [24, 25]. Given that half of Métis citizens, compared to less than 10 % of the general population of Ontario, were found to reside in northern regions with little access to BMD testing, it is not surprising to find that crude as well as sex-specific and age-standardized rates of BMD testing were lower among Métis citizens compared to the general population. This is consistent with prior research on other chronic conditions that has identified lower rates of screening and fewer specialist visits among Métis that may relate to problems with access in remote areas [11–13, 26–28]. Indeed, after adjusting for regional variables (region, urban residence, neighbourhood income quintile), differences in rates of BMD testing disappeared among women. However, differences persisted among men. Prior research identifies higher rates of osteoporosis risk factors such as cardiovascular disease, chronic obstructive pulmonary disease, and diabetes among Métis compared to the general population of Ontario [11-13], and thus, the finding that BMD testing rates were lower among Métis men after adjusting for regional characteristics is puzzling. Indeed, our finding that Métis men had lower age-standardized rates of osteoporosis pharmacotherapy suggests a potential gender gap. Prior research identifies a tight link between BMD testing and osteoporosis treatment initiation [25]. It is thus not surprising to find that lower rates of BMD testing among men would translate into lower rates of pharmacoprevention. Prior research has also found that men have lower rates of post-fracture treatment and glucocorticoid-induced osteoporosis management compared to women [29, 30]. It is thus particularly interesting to find that Métis men have lower rates of BMD testing after adjusting for regional differences in access, compared with men in the general population. Further research to better understand the reasons for lower rates of BMD testing and osteoporosis treatment among Métis men compared to the general population of men is of interest.

Access to BMD testing has been shown to impact pharmacotherapy [25] and thus is proposed to lead to potential inequities in fracture prevention. One interpretation of our findings may therefore be to improve access to BMD testing in northern and rural areas of Ontario. However, despite finding lower age-adjusted rates of BMD testing (both sexes) and pharmacotherapy (men only) among Métis citizens compared to the general population, fracture rates were found to be similar. Although this finding is comforting, our results are limited by not including vertebral fractures. Vertebral fractures are the most common type of osteoporotic fracture and cause significant morbidity [20]; however, less than half come to clinical attention [31, 32]. For this reason, healthcare administrative data are limited in ability to capture vertebral fractures. It is thus possible that a closer examination with X-rays could identify significant differences in vertebral fractures and thus osteoporosis morbidity, particularly among Métis men. Nonetheless, our finding of little difference in fracture rates between the Métis population and general population of Ontario is consistent with prior research that found similar prevalence of osteoporosis or fracture among Métis and all other residents in Manitoba [33]. However, our results contradict findings from research conducted with larger groups of Aboriginal peoples in Manitoba that document significantly higher fracture rates among First Nations after adjusting for age, sex, income, and geographical residence area [34]. Both studies from Manitoba included vertebral fractures, and differences in vertebral fractures among First Nations were largely identified in younger age groups compared to our study that focused on adults aged 50 or more years [34]. Higher fracture rates among First Nations people in Manitoba are proposed to be related to higher prevalence of diabetes, comorbidity, and substance abuse [35] and a higher rate of accidental and non-accidental trauma [34]. Further research into the burden of osteoporosis among distinct groups of Aboriginal peoples (First Nations, Inuit, and Métis) is of interest. Results from Manitoba identified that First Nations people are less likely to receive a BMD test or pharmacotherapy within 6 months post-fracture [36], yet are at higher risk for post-fracture mortality [37]. Due to the small number of Métis citizens with fractures in our study, we were unable to examine post-fracture osteoporosis management or adherence to therapy.

We acknowledge that our study is subject to some limitations. First, given that the Métis citizenship registry is voluntary and requires individuals to provide proof of ancestry, it may not capture the entire Métis population in Ontario and thus misclassify some Métis in the general population. In comparison to the 2011 National Household Survey, our cohort of Métis citizens represents approximately 25 % of the equivalently aged Métis in Ontario and is represented by more men (55 vs. 49 % in the National Household Survey) [3]. Registration with the Métis Nation of Ontario permits citizens to apply for Harvesters Certification that allows holders to hunt and fish [38], a benefit that may be more appealing to male Métis. Nonetheless, by completing analyses separately for men and women and standardizing by age, we were able to adjust for any sex- and age-related differences. In addition, although Métis people not registered with the Métis Nation of Ontario, as well as other Aboriginal peoples (First Nations and Inuit), would be included with the general population estimates, we anticipate little overall impact on estimates of osteoporosis management in the general population since these Aboriginal groups are few in number compared to the large population of older adults in Ontario. Second, the Ontario Drug Benefit database is limited to individuals aged ≥65 years, and thus, we did not have pharmacy data for younger patients. Although we could have restricted our study to persons aged ≥65 years, including men and women aged 50 or more years in our study permitted a more comprehensive comparison of BMD testing and fracture rates. Third, our study was limited by a relatively small sample size of Métis men and women aged 50 or more years, with few overall fractures, and we were unable to examine other osteoporosis risk factors, such as glucocorticoid exposure that may differentially impact osteoporosis management in the Métis and the general population. Finally, our data did not capture vertebral fractures, and thus, we may underestimate differences in rates of some osteoporotic fractures between Métis citizens and the general population. Despite these limitations, we have significant strength in our ability to leverage data for the province of Ontario and in working with the Métis Nation of Ontario and the Public Health Agency of Ontario in their efforts to better understand Métis health.

As the Métis Nation of Ontario registry and other Métis registries grow across Canada, future research may be able to examine comparative rates of osteoporosis management and fractures in a larger and more representative sample of Métis citizens, and in particular, post-fracture osteoporosis management. We recommend that future research aim to clarify the burden of osteoporosis management among different Aboriginal groups, particularly among men; and examine whether regional variation in access to services, such as BMD testing in rural and remote locations, translate into important differences in post-fracture management and adherence to osteoporosis pharmacotherapy.