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Prevalence, determinants and co-morbidities of chronic kidney disease among First Nations adults with diabetes: results from the CIRCLE study
© Dyck et al.; licensee BioMed Central Ltd. 2012
Received: 29 March 2012
Accepted: 18 June 2012
Published: 9 July 2012
Indigenous peoples worldwide are experiencing elevated rates of type 2 diabetes and its complications. To better understand the disproportionate burden of diabetic end stage renal disease (ESRD) among Canadian First Nations people (FN), we examined prevalence, determinants, and co-morbidities of chronic kidney disease (CKD) within this population.
The 2007 Canadian FN Diabetes Clinical Management and Epidemiologic (CIRCLE) study conducted a cross-sectional national medical chart audit of 885 FN adults with type 2 diabetes to assess quality of diabetes care. In this sub-study, participants were divided by estimated glomerular filtration rate (eGFR in ml/min/1.73 m2), as well as by albuminuria level in those with eGFRs = > 60. Those with eGFRs = > 60 and negative albuminuria were considered to have normal/near normal kidney function (non-CKD). Using univariate and logistic regression analysis, they were compared with participants having eGFRs = > 60 plus albuminuria (CKD-alb) and with participants having eGFRs <60 (CKD-eGFR <60).
While 84.5% of total CIRCLE participants had eGFRs = > 60, almost 60% of the latter had CKD-alb. Of the 15.5% of total participants with CKD-eGFR <60, 80% had eGFRs 30–60 (Stage 3 CKD) but over 10% (1.6% of total participants) had ESRD. Independent determinants of CKD-alb were male gender and increasing diabetes duration, systolic BP, A1C and total cholesterol. These plus smoking rates also discriminated between FN with micro- and macro-albuminuria. Independent determinants of CKD-eGFR <60 were increasing age at diabetes diagnosis, diabetes duration, total cholesterol and systolic BP. However, participants with CKD-eGFR <60 also displayed a decreasing mean age of diabetes diagnosis as eGFR declined. Micro-vascular co-morbidities were significantly associated with CKD-alb but both micro- and macro-vascular co-morbidities were associated with CKD-eGFR <60. Only 35-40% of participants with CKD used insulin.
High prevalences of CKD-alb and early CKD-eGFR <60 among diabetic FN were largely related to modifiable and treatable risk factors. However, an earlier age of diabetes diagnosis and longer duration of diabetes characterized those with ESRD. These findings suggest that a failure to meet current standards of diabetes care interacting with an age-related survival benefit contribute to the disproportionate burden of ESRD among FN and possibly other Indigenous peoples.
Rates of diabetic end stage renal disease (ESRD) are disproportionately elevated among Indigenous peoples worldwide [1, 2]. In Canada, the incidence of diabetic ESRD remains three times higher among First Nations people (FN) than others, although disparities have diminished slightly since peaking in the early 1990s . After adjusting for substantially higher diabetes prevalence among FN compared to non-FN , these disparities are characterized by two important observations. First, compared with their non-FN counterparts, a greater proportion of diabetic FN have normal estimated glomerular filtration rates (eGFRs) but a higher prevalence of albuminuria [5–8]. Second, FN are younger at diabetes diagnosis than non-FN and experience a longer duration between diabetes and ESRD diagnoses . These findings suggest that diabetic FN are more prone to the initial development of chronic kidney disease (CKD) and may be more likely to survive long enough to develop ESRD [6, 9].
Although the analysis of administrative [3, 4, 8] and other large databases [10, 11] has greatly enhanced our understanding of the differences between FN and non-FN in the epidemiology of diabetes and ESRD, the possible genetic and environmental factors that underlie the observations summarized above remain unclear. Because the current investigation utilized detailed individual level information gathered as part of the Canadian First Nations Diabetes Clinical Management and Epidemiologic (CIRCLE) study , we were able to conduct the first comprehensive study of prevalence, determinants, treatment and co-morbidities of chronic kidney disease within a broad sample of adult FN people with type 2 diabetes across Canada. The results provide new insights into the development and progression of diabetic renal disease within this population which we hope can be translated into more effective prevention/management initiatives.
Research Design, Ethics Approval and Participant Selection
The methodology used in the CIRCLE study has been previously described . Briefly, we carried out a cross-sectional medical chart audit of 2007 data for 885 FN adults (18 years and older) with type 2 diabetes who lived in 19 First Nations communities across seven provinces in Canada. FN are one of three diverse Indigenous populations of Canada which also include Inuit and Métis. The study was approved by the University of Western Ontario, the University of Toronto and Health Canada Research Ethics Boards as well as by each Band Council and other University ethics review boards as required. Community participation was confirmed by a research agreement after community consultations were held. The Ownership, Control, Access and Possession (OCAP) principles developed by the National Aboriginal Health Organization  were used to guide the ethical conduct of the study.
A registry of all adults with type 2 diabetes was developed in each community. Potential CIRCLE participants were then randomly selected from each community’s registry and sequentially contacted for consent until up to 50 people had agreed to participate. For the final analyses, medical chart auditing was successfully carried out by trained local research assistants on 885 of 950 potential study participants.
Data Collection and Definition of Chronic Kidney Disease Sub-Groups
Charts were audited for participant characteristics, a range of diabetes quality care indicators derived from clinical practice guidelines (CPG) , pharmacologic treatment and the presence of co-morbidities that are defined and described in more detail elsewhere (12). Audits were carried out in 2008/09 for the latest healthcare information available for 2007 which was based on a mean of 8.7 visits per participant. If data was missing for 2007, the most recent value prior to that year was used. All information was de-identified and entered into an Access database using study identification numbers.
CIRCLE participants were sub-divided into groups based on their estimated glomerular filtration rates (eGFR) and urinary excretion of albumin. Because test results were obtained from medical chart records, methods for measuring serum creatinine and urine parameters were those being used by the particular province rather than being carried out in one centralized laboratory. eGFRs were calculated using an equation based on the original Modification of Diet in Renal Disease Study Group (MDRD) equation which uses age, sex, serum creatinine, and black/white ethnicity . Thus for males: eGFR = 186 x (serum creatinine x 0.0113)-1.154 x age (years)-0.203 and for females: eGFR = 186 x (serum creatinine x 0.0113)-1.154 x age (years)-0.203 x 0.742. For ethnicity, we used the unadjusted (white ethnicity) parameter which has been preliminarily validated in a North American Indian population . Only those who had at least one serum creatinine result during the study year were included in this sub-study. When more than one result was available, we utilized the lowest value to avoid results possibly associated with acute renal impairment.
The eGFR sub-groups were based on chronic kidney disease (CKD) stages  using the Kidney Disease Outcomes Quality Initiatives classification (eGFR = > 90 ml/min per 1.73 m2 = no CKD and stage 1, 60–89.9 = no CKD and stage 2, 30–59.9 = stage 3, 15–29.9 = stage 4, <15 = stage 5). Those with an eGFR <15 who were not receiving renal replacement therapy (stage 5a) were combined with stage 4 because of small numbers, while people receiving renal replacement therapy were classified as stage 5b. Finally, because there are particular limitations to the MDRD eGFR equation at eGFRs = > 60ml/min/1.73m2 (see DISCUSSION), we presented both overall data for those with eGFRs = > 60ml/min/1.73m2 as well as sub-group information for those with eGFRs = > 90 and 60–90ml/min. Those with an eGFR = > 60 were further sub-divided by the presence or absence of albuminuria . Micro-albuminuria was defined as a 24h urine value 30–300mg/day for both sexes, or a urine albumin: creatinine ratio (ACR) of 2.0-20.0mg/mmol for males, or an ACR of 2.8-28mg/mmol for females. Macro-albuminuria was defined as a 24h urine value >300mg/day for both sexes, an ACR >20.0 mg/mmol for males or an ACR >28 mg/mmol for females. Ten individuals without an available ACR record were considered to have micro-albuminuria because of a chart diagnosis by a physician.
After determining the distribution of CIRCLE participants by eGFR stage (all) and by albuminuria positivity (those with eGFRs = > 60ml/min), we defined three groups for further comparisons. Those with normal or near-normal kidney function (non-CKD) had eGFRs = > 60ml/min/1.73m2 and negative albuminuria. CKD was defined on the basis of positive albuminuria in those with eGFRs = > 60ml/min/1.73m2 (CKD-alb) or an eGFR <60ml/min/1.73m2 regardless of albuminuria (CKD-eGFR <60). All subsequent comparisons were between people with either CKD-alb or CKD-eGFR <60 and those with non-CKD; we compared overall groups as well as subgroups defined by eGFR stage.
The following parameters were compared between groups and sub-groups: gender; mean age at audit and diabetes diagnosis, and duration of diabetes; mean body mass index (BMI); proportion of smokers; mean systolic blood pressure (sBP); mean diastolic blood pressure (dBP); mean glycosylated haemoglobin (A1C), mean total cholesterol (TC); mean low density lipoprotein cholesterol (LDL); mean high density lipoprotein cholesterol (HDL); proportions with micro-vascular and macro-vascular co-morbidities (total and by organ system); and proportions receiving treatment with insulin and/or agents that target the renin/angiotensin/aldosterone system (RAAS).
Univariate analyses employed chi square tests to compare proportions and two tailed t-tests to compare means. We also used trend analysis to compare selected parameters by level of albuminuria (negative, micro-albuminuria, macro-albuminuria) in those with eGFRs = > 60ml/min. Finally, multivariate analysis was carried out by entering potential determinants of CKD-alb or CKD-eGFR <60 (versus non-CKD) into a logistic regression model. Statistical tests were conducted using PASW Statistics version 18.0 and p <0.05 was used to determine significance. Odds ratios (OR) and 95% confidence intervals (CI) were determined in multivariate analyses.
Circle participants by eGFR* category and urine albumin testing
eGFR = > 90
eGFR 60 to <90
eGFR 30 to <60
eGFR 15 to <30
eGFR <15 (no RRT**)
eGFR <15 (RRT)
Non/Stage 1 CKD
Non/Stage 2 CKD
Stage 3 CKD
Stage 4 CKD
Stage 5a CKD
Stage 5b CKD
People with eGFR (% total)
People with eGFR & Urine Albumin Test (% total)
Normal Urine Albumin (% in eGFR Stage)
Micro-albuminuria (% in eGFR Stage)
Macro-albuminuria (% in eGFR Stage)
Micro/Macro-albuminuria (% in eGFR Stage)
People included in further analyses (% total)***
Characteristics of Circle participants by eGFR category and urine albumin (Ua) positivity (+/−) when eGFR = > 60
PARAMETER* (Mean values or %)
eGFR = < 90
eGFR 60 - < 90
eGFR = > 60 Total**
eGFR 30 - <60
eGFR <30 (no RRT)
eGFR <15 RRT
All eGFR < 60 = CKD-eGFR <60
Stage 3 CKD
p vs Non-CKD
Stage 4/5a CKD
p vs Non- CKD
Stage 5b CKD
p vs Non- CKD
Stage 3-5b CKD
p vs Non- CKD
AGE AT AUDIT
sBP (mm Hg)
dBP (mm Hg)
A1C (mean %)
All Macrovasc (%)
% periph vasc
% cerebro vasc
% combined heart
All Microvasc (%)
% foot disease
% eye disease
% RAAS agents
Mean sBP was higher among those with CKD-alb than non-CKD (133.3 versus 128.7 mm Hg; p < 0.001) but mean dBP was similar. Mean A1C was almost one percentage higher in those with CKD-alb compared to those with non-CKD (8.68 versus 7.72; p < 0.0001), while the mean TC was the only lipid value that was significantly higher among those with CKD-alb. Microvascular but not macrovascular complications were significant co-morbidities associated with CKD-alb. Finally, almost 35% of CKD-alb participants were receiving insulin therapy and almost 80% were on RAAS agents. These proportions were significantly higher than those for non-CKD.
With respect to participants having an eGFR = > 60 ml/min, those with an eGFR = > 90 were younger at time of diabetes diagnosis, and had a shorter duration of diabetes than those with an eGFR from 60 to <90 ml/min. Those with a higher eGFR also had higher A1C values; the worst A1C levels were in those with eGFRs = > 90 ml/min/1.73 m2 and positive albuminuria (8.95 versus 8.05 in those with no albuminuria; p < 0.0001).
Table 2 – Characteristics of participants with CKD-eGFR ≤60 and comparison with non-CKD participants: There continued to be a female predominance overall but 7 of 8 people on dialysis were male. While the mean age at diabetes diagnosis for people with an eGFR 30 to <60 ml/min/1.73 m2 (stage 3 CKD) was almost 10 years older than non-CKD participants (52.95 versus 43.62 years; p < 0.0001), the mean age at diabetes diagnosis of people with eGFRs <30 ml/min/1.73 m2 was younger (42.17 for those in Stage 4/5a and 35.88 for those in Stage 5b). This was associated with a longer duration of about 20 years from diabetes diagnosis in the latter two groups compared to 14.3 years for those with stage 3 CKD.
Participants with CKD-eGFR <60 were slightly less obese and had significantly lower smoking rates than those with non-CKD. Mean sBP was significantly higher but mean dBP was significantly lower compared to non-CKD. There were no overall differences in A1C or lipid values between people with CKD-eGFR <60 and non-CKD; however, the mean A1C level was significantly lower among those on dialysis (6.25 versus 7.72; p = 0.033). In contrast to participants with CKD-alb, those with CKD-eGFR <60 not only experienced a higher frequency of microvascular but also of macrovascular co-morbidities.
Characteristics of Circle participants with eGFR = > 60 by degree of albuminuria
People With eGFR = > 60 and Urine Albumin (UA) Test
Total With UA
UA neg (non-CKD)
AGE AT AUDIT – mean (SD)
at diabetes diagnosis – mean (SD)
diabetes duration – mean (SD)
BODY MASS INDEX – mean (SD)
sBP mm Hg – mean (SD)
dBP mm Hg – mean (SD)
AIC % – mean (SD)
TC mM – mean (SD)
LDL mM – mean (SD)
HDL mM – mean (SD)
% eye disease
% RAAS agents
People with any level of albuminuria had a significantly higher mean sBP (>130 mm Hg) than those with non-CKD (128.7 mm Hg) but mean dBP’s were similar and normal (<80 mm Hg) in all groups. There was a progressive and highly significant increase in mean A1C by increasing amounts of albuminuria, from 7.72% in those with no albuminuria to 8.34% and 9.58% in those with micro- and macro-albuminuria respectively (<0.0001). TC also increased progressively from 4.38 mmol/L in those with non-CKD to 4.49 and 4.93 mmol/L in those with micro- and macro-albuminuria respectively (<0.0001). Participants with macro-albuminuria also had significantly higher levels of LDL and HDL cholesterol.
The proportion of CIRCLE participants with eye disease and neuropathy increased progressively and significantly by level of albuminuria from under 8% in those with no albuminuria to over 18% in those with macro-albuminuria. Finally, although use of both insulin and RAAS agents increased significantly with degree of albuminuria, only 39.4% of those with macro-albuminuria were on insulin while over 90% of that group were taking RAAS agents.
Adjusted odds ratios (OR) for associations between model variables and chronic kidney disease*
People With eGFR ≥60 and Albuminuria (CKD-alb) versus Non-CKD
People With eGFR <60 (CKD-eGFR <60) versus Non-CKD
Gender (male versus female)
Diabetes Diagnosis Age (per year ↑)
Diabetes Duration (per year ↑)
Body Mass Index (per 1 unit ↑)
Smoker (yes versus no)
Systolic BP (per 1 mmHg ↑)
Diastolic BP (per 1 mmHg ↑)
A1C (per 0.1% ↑)
Total Cholesterol (per 0.1 mM ↑)
While recent reports have examined the relationship between chronic kidney disease (CKD) and diabetes in other North American indigenous populations [18–20], this is the most comprehensive study of prevalence, determinants and co-morbidities of chronic kidney disease (CKD) that has been carried out among adult First Nations people (FN) with type 2 diabetes in Canada. It is also the first to include a broad representation of FN communities from across the country. We have confirmed that a large majority of diabetic FN have normal or near normal eGFRs but experience high rates of albuminuria [5–8], and that those who develop ESRD are characterized by a younger age at diabetes diagnosis and a longer exposure to the metabolic consequences of diabetes [3, 9]. What we now show more clearly than previously reported is that the initial development of CKD in this population is strongly related to modifiable and treatable risk factors despite possible genetic and prenatal precursors. Furthermore, the development of ESRD appears dependent on factors contributing to long term survival of a small minority rather than to rapid progression of CKD.
Almost 60% of diabetic FN with eGFRs = > 60 ml/min/1.73 m2 in our study had micro- or macro-albuminuria (CKD-alb) and this was clearly associated with suboptimal diabetes management. Thus, we not only demonstrated for the first time in this population that increasing A1C, sBP, and TC were all independent determinants of CKD-alb but that progressive increases in A1C and TC also discriminated between those with micro- and macro-albuminuria, with the latter group having mean A1C’s >9.5%. Additionally, over 50% of those with macro-albuminuria were smokers, more than 10 percentage points higher than those with micro-albuminuria or non-CKD. It is thus concerning to note that smoking rates were also very high among the youngest sub-group in our study, those with eGFRs 90 and higher. Interestingly, increasing BMI was not associated with CKD-alb and those with macro-albuminuria had lower BMI’s than others. This might be due to weight loss associated with very poor glycemic control and/or, because of their inadequate usage, lack of the weight gain often related to glucose lowering drugs.
A longer duration of diabetes and male gender were also independent determinants of albuminuria. The impact of disease duration was expected but has not been previously shown in this population. Similarly, while a higher frequency of albuminuria has been reported among male FN with diabetes , this is the first time that male gender has been identified as an independent determinant of albuminuria among FN. Those with macro-albuminuria, which included the highest proportion of males, also had the highest A1C, TC and smoking rates. Therefore, it is likely that differences in lifestyle and diabetes management rather than underlying biologic differences largely account for the impact of gender on development of albuminuria.
This study also provides insights into why diabetic FN experience a higher risk for ESRD. Although independent determinants of an eGFR <60 ml/min/1.73 m2 included increases in age at diabetes diagnosis, duration of diabetes, sBP and TC, we found that the mean age at diabetes diagnosis actually decreased from 53.0 years for those with Stage 3 CKD to 35.9 years for those with Stage 5b CKD. Furthermore, there was a reversal in the female: male ratio from predominantly females in Stage 3 to overwhelmingly males in Stage 5b. These are consistent with Saskatchewan findings  and are most obviously explained by an age-related survival effect whereby those younger at diabetes diagnosis were more likely to survive after reaching Stage 3 CKD. Unlike overall mortality rates among diabetic FN which tend to be worse for males , our findings from this and previous studies [3, 6] suggest that mortality during the late stages of diabetic CKD appears to be higher for females. Importantly, we have now provided evidence that differential mortality likely contributes to both ethnicity-based disparities in development of diabetic ESRD  as well as to ESRD risk within FN populations.
As we and others have reported [6, 22], mean A1C levels actually decreased with declining eGFRs and were lowest (6.25%) in those requiring RRT. This observation may be due to uremia-related appetite suppression and nutritional problems as supported by a parallel decline in BMI, or to a reduction in exogenous insulin requirements related to declining renal function. Since it has recently been shown that A1C values <6.5% are associated with increased mortality among those with diabetic CKD , this may be a factor in the poor median survival of both FN and non-FN with diabetic ESRD .
While only micro-vascular comorbidities were significantly associated with CKD-alb, both micro- and macro-vascular comorbidities were related to CKD-eGFR <60. The first finding is presumably due to the impact of poor glycemic control on the development and progression of micro-vascular complications [23, 24]. The second finding is also important because the association of macro-vascular co-morbidities with worsening eGFR relates to both the underlying pathophysiology of these complications and the implications for those with eGFRs <60 ml/min. Thus, increasing TC, sBP and diabetes duration were all independent determinants of CKD-eGFR <60, but are also known risk factors for macro-vascular complications and death in those with diabetes [25, 26]. Furthermore, impaired renal function also contributes to the development of macro-vascular complications and death [27, 28]. Accordingly, our findings not only provide a plausible explanation for mechanisms contributing to the development of CKD-eGFR <60 and its co-morbidities, but also for the attendant increase in mortality rates. Combined with the higher AIC levels that we identified in those with earlier stages of CKD and that have also been shown to be independently associated with death in those with CKD , it is not surprising that only a select minority of people with diabetes live long enough to develop ESRD and that this survivorship particularly favours those with a younger age of diabetes onset.
Although people with CKD-alb and CKD-eGFR <60 were more likely to be on insulin and RAAS agents than people with non-CKD, only the 80% on RAAS agents approached Canadian Diabetes Association CPG guidelines recommending their use in those with CKD . In contrast, only about 1/3 of FN with CKD were on insulin – in the context of a mean A1C >8% for the total study population and over 9.5% in those with macro-albuminuria, these results indicate a critical need for improvements in glycemia management. This is particularly concerning when guidelines recommend insulin therapy in those with A1Cs consistently >9%  and when we have previously shown that diabetic FN are less likely than their non-FN counterparts to achieve a target A1C of 7% . Finally, while we did not analyze the use of lipid lowering agents in this sub-study, over 70% of CIRCLE participants with an LDL >2.5% were receiving pharmacologic treatment. As we have noted previously , LDL values tend to be closer to target than other diabetes quality care indicators among FN and may not adequately reflect dyslipidemia in this population. Instead, TC was an independent determinant of both CKD-alb and CKD-eGFR <60.
Strengths of this study included its national scope, randomized approach to participant selection, ability to only include those with type 2 diabetes and use of detailed individual level information. Limitations included the use of opportunistic rather than random sampling of FN communities across Canada. Thus, study results do not necessarily represent the findings of all FN people with diabetes in Canada. For example, we observed a smaller proportion of CIRCLE participants requiring RRT compared to their Saskatchewan FN counterparts , possibly because of difficulty contacting such individuals who frequently travel to or have relocated to larger centers where dialysis facilities are available. Second, we were unable to identify CKD with causes other than diabetes and did not have complete data with respect to urine albumin testing. Third, in some cases, a diagnosis of CKD-alb or CKD-eGFR <60 may have been made on the basis of a single urine albumin or serum creatinine test result and we can not rule out the possibility that some abnormal results were due to acute rather than chronic renal problems. Fourth, although few cases of albuminuria were based on 24 hour urine collections, over- or under- collection of urine could have increased or decreased urine albumin values respectively. Fifth, there are limitations to the MDRD eGFR equation particularly at eGFRs = > 60 ml/min/1.73 m2[30–32]. Accordingly, we have presented both overall data for those with eGFRs = > 60 ml/min/1.73 m2 as well as sub-group information for those with eGFRs = > 90 and 60–90 ml/min. Finally, our cross-sectional design did not allow the longitudinal follow up of people as they transitioned from diabetes diagnosis through the CKD stages. Importantly, this did not permit us to determine mortality rates by diabetes duration, eGFR and presence of albuminuria. The latter information would have allowed us to further clarify the impact of differential mortality related to the competing risks of ESRD and death. In addition, the cross-sectional design prevents us from making causal inferences and the use of the terms “determinant” and “co-morbidity” is not intended to imply that our findings have established a cause-effect relationship.
Our results demonstrate that, despite the role of genetic [33, 34] and pre-natal factors  in the development of diabetic kidney disease among Indigenous North Americans, the development of albuminuria was more immediately related to quality of diabetes care and other modifiable risk factors such as smoking. Failure to achieve or even approach CPG targets for glycemic, systolic blood pressure and possibly cholesterol control clearly discriminated between those with and without albuminuria and was related to obvious deficiencies in pharmacologic and lifestyle interventions. Why a small proportion of those with early diabetic nephropathy progressed to eGFRs <60 ml/min/1.73 m2 also appeared related to quality of diabetes care, but increasing age and duration of diabetes also emerged as dominant factors. Of particular importance in explaining the development of diabetic ESRD, those with this devastating complication were almost 20 years younger at age of diabetes diagnosis than those with Stage 3 CKD. The most plausible explanation for this observation was an age-related survival benefit that allowed those with an earlier age of diabetes onset to live long enough to develop ESRD. This requires confirmation using longitudinal studies that analyze the competing risks of ESRD and death from the age of diabetes diagnosis. Nonetheless, the overall message is clear. Rate disparities in diabetic ESRD and earlier CKD Stages both within FN populations and between FN and others are potentially remediable through early diagnosis of diabetes, smoking cessation and by meeting established CPG targets for glycemic, blood pressure and cholesterol control. Finally, this study once again highlights the need for communities and health care systems to promote healthy lifestyles and develop effective primary prevention initiatives [36, 37]. It is possible that even delaying the onset of diabetes among FN could substantially reduce the incidence of ESRD.
Funding for the CIRCLE study was generously provided in the form of a Contribution Agreement from the Aboriginal Diabetes Initiative (ADI), First Nations and Inuit Health Branch (FHIHB), Health Canada. The funding bodies had no role in the study or in this article.
The authors would also like to acknowledge all the site investigators, Aboriginal communities, Band Councils and community research assistants who participated in the CIRCLE study as well as the statistical assistance of Selam Mequanint.
The CIRCLE Study Group
British Columbia , Site Investigator: Dr. Keith Dawson. Research Assistants: Sue Gladstone, Laurel deGoeij, Kelly Legere.
Alberta , Site Investigator: Dr. Ellen Toth. Research Assistants: Natalie White Quills, Darci Healy, Theresa Campiou, Brenda Laboucan, Pam Cooke, Daniel Wildcat.
Saskatchewan , Site Investigator: Dr. Roland Dyck. Research Assistants: Wendy McKenzie, Teresa McLeod.
Manitoba , Site Investigator: Dr. Nichole Riese. Research Assistants: George Flett, Cheyanne Harper.
Ontario , Site Investigators: Dr. Bernard Zinman, Dr. Onil Bhattacharyya, Dr. Michael Green, Dr. Anthony Hanley. Coordinating Centre: Dr. Stewart Harris, Mariam Naqshbandi Hayward, Jim Esler, Marnie Orcutt. Research Assistants: Elizabeth Estey, Peggy Sugarhead, Denise Troutlake, Linda Nakogee, Tom McLeod, Tina McLeod, Sharon Dockstater, Vikki Tran, Laverne Fiddler, Marie-Elaine Delvin.
Quebec , Site Investigators: Dr. David Dannenbaum, Ms. Joceline Piché, Dr. Darlene Kitty, Dr. Laura MacLaren, Dr Ann C Macaulay. Research Assistants: Jean-Pierre Desormiers, Cindy Chakapash, Lisa Bobbish, Dawn Montour-Lazare, Cynthia Deere.
Newfoundland and Labrador , Site Investigator: Ms. Kayla Collins. Research Assistant: Maggie Organ
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