Emerging diabetes and metabolic conditions among Aboriginal and Torres Strait Islander young people
Abstract
Intersectoral collaboration is needed to engage communities and design effective culturally and age-appropriate interventions The gap between the health of Aboriginal and Torres Strait Islander and non-Indigenous Australians is well documented, with many policies and programs currently working towards improving outcomes. Despite these efforts, life expectancy is 10–11 years less than that of non-Indigenous Australians,1 and 65% of deaths occur before 65 years of age, compared with 19% in the non-Indigenous population.1 Cardiovascular and metabolic diseases are responsible for most of the gap in life expectancy and are associated with higher hospitalisation and mortality rates.1 In 2013, hospitalisation rates for cardiovascular disease were 1.6–2.5 times higher in Indigenous people depending on age, and Indigenous adults are six times as likely to die from diabetes as non-Indigenous Australians.1 Indigenous adolescents with type 2 diabetes are over ten times more likely to be hospitalised than non-Indigenous adolescents.2 While we acknowledge that hospitalisations are a poor indicator of the true prevalence of diabetes-related complications within the community, they suggest that the burden of disease associated with a diagnosis of diabetes is greater in the Aboriginal and Torres Strait Islander population.1 Importantly, the age of onset of cardiometabolic conditions, such as diabetes, obesity and cardiovascular disease, is significantly younger in Indigenous than in non-Indigenous Australians, and the incidence of these conditions continues to increase in Indigenous youth.3 With limited national data currently available, however, the prevalence of type 2 diabetes among Indigenous young people is not known. Studies from different states consistently report higher rates, from a younger age, of youth onset type 2 diabetes in the Indigenous Australian population.3-5 While we have seen an increasing prevalence among all Australian youth over the past 20 years, Indigenous young people have experienced a much greater rise in new diagnosis rates. Western Australian data indicate a disturbing discrepancy, with a type 2 diabetes incidence of 12.6 per 100 000 person years in Indigenous youth aged 16 years or less, compared with an incidence of 0.6 in non-Indigenous youth — a striking 20-fold difference.3 A 2007 New South Wales study suggested that type 2 diabetes was 6.1 times as common among Indigenous young people aged 0–19 years than among non-Indigenous young people,4 and a 2013 Northern Territory study reported that Indigenous youth represented 88% of youth type 2 diabetes diagnoses.5 These statistics indicate the extent of the issue despite likely diagnostic underestimation, as many children with type 2 diabetes may be managed in primary care rather than by paediatric or diabetes services, or are not diagnosed until a later age.5 The increasing incidence in the young Indigenous Australian population parallels the global context, where type 2 diabetes in youth has been described as an avoidable "disease of poverty" concentrated in populations of socio-economically disadvantaged young people.6 Risk factors for diabetes and metabolic syndrome have been reported at a significantly earlier age and at much higher frequency among the Indigenous Australian population,7, 8 suggesting that the prevalence of diabetes will continue to rise exponentially in the future without intervention. In Indigenous Australian young people with type 2 diabetes, there are also higher rates of comorbidities, with 59% also having hypertension, 24% having dyslipidaemia and 61% having obesity.3 These comorbidities will have a significant impact on the future burden of disease, and may lead to renal, cardiac, neurological and ophthalmological complications. Canadian data demonstrated that 45% of patients with youth onset type 2 diabetes had reached end-stage renal failure, requiring renal replacement therapy, 20 years after diagnosis, compared with zero people with type 1 diabetes.9 Youth onset type 2 diabetes was associated with a 23 times higher risk of kidney failure and 39 times higher risk of need for dialysis, compared with young people without diabetes.9 This implies that many young people who are being diagnosed with diabetes now will be on dialysis by 30 years of age, with significant effects on Aboriginal and Torres Strait Islander families and communities. Global reports also suggest that the pathophysiology, phenotype, treatment response and prognosis of youth onset diabetes differ significantly from later onset diabetes.10 This contributes to greater concern regarding the future health of young people, as youth onset diabetes (defined as that diagnosed before the age of 25 years) appears to progress more rapidly, be more difficult to treat, have more comorbidities, and have a higher risk of complications. There is also a greater risk of mental health concerns, and the diagnosis of diabetes appears to worsen any pre-existing comorb
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The discrepancy in external validation underscores the potential influence of region- and population-specific factors on model transferability.
“This discrepancy underscores the potential influence of region- and population-specific factors on model transferability, such as differences in dietary patterns, genetic susceptibility, and variations in metabolic phenotypes [38–41].”
From Machine learning with the body roundness index and associated indicators: a new approach to predicting metabolic syndrome (2025) · cites this paper as [40]
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- Authors
- Titmuss, A., Davis, E. A., Brown, A., & Maple‐Brown, L. J.
- Affiliations
- Menzies School of Health Research (AU)
- Princess Margaret Hospital for Children (AU)
- University of South Australia (AU)
- Royal Darwin Hospital Darwin NT
- Corresponding author
- Titmuss, Angela
- Venue
- Medical Journal of Australia
- Publisher
- Wiley
- Published
- 2019-01-18
- Volume
- 210
- Issue
- 3
- Pages
- 111
- ISSN
- 0025-729X (ISSN-L)
- 1326-5377
- OpenAlex
- W2914324501
- Cited by
- 54
- References
- 17
- Citations by year
- 2026: 1 · 2025: 9 · 2024: 8 · 2023: 5 · 2022: 8 · 2021: 11 · 2020: 10 · 2019: 2
- FWCI
- 7.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- The Medical Journal of Australia (publishedVersion)
- PubMed (publishedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- Funders
- National Health and Medical Research Council (1131932, 1137563, 1078477)
- Topics
- Social Sciences › Health › Indigenous Health, Education, and Rights
- Health Sciences › Health Professions › General Health Professions › Indigenous Health and Education
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Obesity, Physical Activity, Diet
- Keywords
- diabetes mellitus, metabolic disorders, Aboriginal and Torres Strait Islander peoples, youth, Indigenous health
- MeSH terms
- Australian Aboriginal and Torres Strait Islander Peoples, Adolescent, Adult, Australia, Child, Diabetes Mellitus, Type 2, Humans, Hypertension, Obesity, Risk Factors, Native Hawaiian or Other Pacific Islander, Dyslipidemias, Young Adult
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