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Exploring clinical predictors of cardiovascular disease in a central Australian Aboriginal cohort
Joanne N Luke1, Alex D Brown, Laima Brazionis
1Onemda VicHealth Koori Health Unit, Centre for Health and Society, School of Population Health, University of Melbourne, Australia. jnluke@unimelb.edu.au
Insights
Predicting cardiovascular disease (CVD) risk in Aboriginal populations is challenging. A combination of hyperglycemia, dyslipidemia, hypertension, albuminuria, and smoking effectively identifies individuals at high risk.
Area of Science:
- Public Health
- Epidemiology
- Cardiology
Background:
- Existing cardiovascular disease (CVD) risk prediction algorithms are limited for Aboriginal populations.
- Novel risk factors associated with insulin resistance and metabolic syndrome require examination for CVD prediction.
Purpose of the Study:
- To identify conventional and novel risk factors for cardiovascular disease (CVD) in Aboriginal people.
- To assess the relationship between these risk factors and subsequent CVD events.
Main Methods:
- Longitudinal cohort study of 739 Aboriginal people in Central Australia (surveys in 1995 and 2005).
- Principal components analysis (PCA), regression, and univariate analyses were used to identify CVD predictors.
Main Results:
- PCA identified five key components: lipids/liver function, insulin resistance, blood pressure/kidney function, glucose tolerance, and anti-inflammatory markers.
- Insulin resistance, blood pressure, glucose tolerance, and age were significant independent predictors of CVD.
- A combination of three or more risk variables (hyperglycemia, dyslipidemia, hypertension, albuminuria, smoking) showed 82.0% sensitivity and 59.9% specificity for predicting incident CVD.
Conclusions:
- Age is the strongest predictor of CVD in this population.
- Screening for a combination of hyperglycemia, dyslipidemia, hypertension, albuminuria, and smoking is an efficient strategy for identifying high-risk individuals.
Introduction:
For Aboriginal populations, predicting individuals at risk of cardiovascular disease (CVD) is difficult due to limitations and inaccuracy in existing risk-prediction algorithms. We examined conventional and novel risk factors associated with insulin resistance and the metabolic syndrome and assessed their relationships with subsequent CVD events.
Design:
Longitudinal cohort.
Methods:
Aboriginal people (n = 739) from Central Australia completed population-based risk-factor surveys in 1995 and were followed up in 2005. Principal components analysis (PCA), regression and univariate analyses (using ROC defined cut-off points) were used to identify useful clinical predictors of primary CVD.
Results:
PCA yielded five components: (1) lipids and liver function; (2) insulin resistance; (3) blood pressure and kidney function; (4) glucose tolerance; and (5) anti-inflammatory (low fibrinogen, high HDL cholesterol). Components 2, 3 and 4, and age were significant independent predictors of incident CVD, and smoking approached significance. In univariate analysis fasting glucose ≥ 4.8 mmol/l, total:HDL cholesterol ratio ≥ 5.7, non-HDL cholesterol ≥ 4.3 mmol/l, gamma-glutamyl transferase ≥ 70 U/l, albumin creatinine ratio ≥ 5.7 mg/mmol, systolic blood pressure ≥ 120 mmHg and diastolic blood pressure ≥ 70 mmHg were useful predictors of CVD. The co-occurrence of three or more risk variables (fasting glucose ≥ 4.8 mmol/l, total:HDL cholesterol ratio ≥ 5.7, blood pressure (systolic ≥ 120 mmHg; diastolic ≥ 70 mmHg; albumin:creatinine ratio ≥ 5.7 mg/mmol and smoking) had sensitivity of 82.0% and specificity of 59.9% for predicting incident CVD.
Conclusion:
Age is the strongest predictor of CVD for this population. For clinical identification of individuals at high risk, screening for the combination of three or more of hyperglycaemia, dyslipidaemia, hypertension, albuminuria and smoking may prove a useful and efficient strategy.
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