Variation in real world dementia risk profiles according to demographic characteristics in 6171 adults drawn from the Australian CogDrisk website

We aimed to evaluate differences in dementia risk profiles according to age, birthplace and First Nations status. The sample included 6171 (62% female, < 1% non-binary/other) middle-aged and older adults who self-administered the CogDrisk assessment online and consented to their data being used for research from May 2023 to May 2024. The majority were aged 40–64 (‘midlife’; 67.9%) or aged 65–96 (‘later-life’; 25.8%); 6.3% were aged 18–40. More than a third (36.2%) were born overseas, 95% resided in Australia, and 66.0% had a university degree. Key midlife risk factors were hypertension 27.7%, pesticide exposure 24.6%, high cholesterol 25.1%, head injury 15.3%, diabetes 7.6%, and atrial fibrillation (AFib) 7.3%. Key later-life risk factors were hypertension 45.4%, pesticide exposure 33.0%, AFib 18.3% head injury 16.4%, and diabetes 11.7%. Midlife respondents born in the Pacific and New Zealand (NZ) had high rates of vascular risk factors and those born in NZ reported high rates of head injury and depression. The highest rates of heavy drinking and insufficient physical activity were reported by respondents born in the UK and Asia respectively. Using published estimates from validation studies, 20% of those aged 65 + had a high dementia risk (CogDrisk score > 12). High rates of multiple risk factors were identified and varied according to age group and birthplace. This study provides evidence for tailoring risk reduction intervention and advice by age and birthplace.

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Journal
BMC Public Health
Published
2025-12-13
DOI
https://doi.org/10.1186/s12889-025-25943-8
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
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article

Variation in real world dementia risk profiles according to demographic characteristics in 6171 adults drawn from the Australian CogDrisk website

Scherazad Kootar, Meiwei Li, Jeromey Temple, Marita Long et al.
BMC Public Health
Dementia and Cognitive Impairment Research
article

Variation in real world dementia risk profiles according to demographic characteristics in 6171 adults drawn from the Australian CogDrisk website

Scherazad Kootar, Meiwei Li, Jeromey Temple, Marita Long, Claire O’Connor, Michael S. Cartwright, Kaarin Jane Anstey, Ranmalee Eramudugolla, Md Hamidul Huque
article en

Abstract

We aimed to evaluate differences in dementia risk profiles according to age, birthplace and First Nations status. The sample included 6171 (62% female, < 1% non-binary/other) middle-aged and older adults who self-administered the CogDrisk assessment online and consented to their data being used for research from May 2023 to May 2024. The majority were aged 40–64 (‘midlife’; 67.9%) or aged 65–96 (‘later-life’; 25.8%); 6.3% were aged 18–40. More than a third (36.2%) were born overseas, 95% resided in Australia, and 66.0% had a university degree. Key midlife risk factors were hypertension 27.7%, pesticide exposure 24.6%, high cholesterol 25.1%, head injury 15.3%, diabetes 7.6%, and atrial fibrillation (AFib) 7.3%. Key later-life risk factors were hypertension 45.4%, pesticide exposure 33.0%, AFib 18.3% head injury 16.4%, and diabetes 11.7%. Midlife respondents born in the Pacific and New Zealand (NZ) had high rates of vascular risk factors and those born in NZ reported high rates of head injury and depression. The highest rates of heavy drinking and insufficient physical activity were reported by respondents born in the UK and Asia respectively. Using published estimates from validation studies, 20% of those aged 65 + had a high dementia risk (CogDrisk score > 12). High rates of multiple risk factors were identified and varied according to age group and birthplace. This study provides evidence for tailoring risk reduction intervention and advice by age and birthplace.

BMC Public HealthVol. 26(1)
The University of Melbourne (AU), UNSW Sydney (AU), Sydney Children’s Hospitals Network (AU), Neuroscience Research Australia (AU)
Openalex Percentile: Top 53%
Dementia and Cognitive Impairment Research
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