Monica Cations1,2, Brian Draper2,3, Lee-Fay Low4, Kylie Radford5,6, Julian Trollor7,8, Henry Brodaty2,3,7, Perminder Sachdev2,7,9, Peter Gonski1,10, Gerald Anthony Broe5,6, Adrienne Withall1. 1. School of Public Health and Community Medicine, UNSW Sydney, Sydney, NSW, Australia. 2. Dementia Centre for Research Collaboration, School of Psychiatry, UNSW Sydney, Sydney, NSW, Australia. 3. Academic Department for Old Age Psychiatry, Prince of Wales Hospital, Randwick, NSW, Australia. 4. Faculty of Health Sciences, University of Sydney, Sydney, NSW, Australia. 5. Neuroscience Research Australia, Sydney, NSW, Australia. 6. School of Medical Sciences, UNSW Sydney, Sydney, NSW, Australia. 7. Centre for Healthy Brain Ageing, UNSW Sydney, Sydney, NSW, Australia. 8. Department of Developmental Disability Neuropsychiatry, School of Psychiatry, UNSW Sydney, Sydney, NSW, Australia. 9. Neuropsychiatric Institute, Prince of Wales Hospital, Randwick, NSW, Australia. 10. Division of Aged and Extended Care (Southcare), Sutherland Hospital, South Eastern Sydney Local Health District, Sydney, NSW, Australia.
Abstract
BACKGROUND: Several brain reserve, vascular risk, and other modifiable factors have been associated with late-onset dementia, but their association with young onset dementia (YOD) has not been adequately explored. OBJECTIVE: To examine the association of cognitive reserve enhancing factors, cardiovascular risk factors (including smoking), depression, alcohol use, and traumatic brain injury (TBI) with non-autosomal dominant degenerative and/or vascular YOD. METHODS: Data for this matched case-control study were taken from two larger studies conducted in NSW, Australia. One comprised all people with YOD within a geographical region, while the other exclusively included Aboriginal and Torres Strait Islander participants. Dementia diagnosis was confirmed by clinical consensus, and risk exposure was retrospectively self- and/or informant-reported. RESULTS: Participants were 96 people with YOD (58.4% with probable Alzheimer's disease) and 175 age-group, sex, and sample matched control participants. Poor educational attainment, low participation in cognitive leisure activity, stroke, transient ischemic attack, and self-reported very heavy alcohol use were related to the risk of primary degenerative and/or vascular YOD. The effect of hypertension and depression varied depending on when they occurred relative to dementia onset. Current smoking was significantly associated with risk in univariate analyses but did not retain significance in multivariate modelling. There was no association with hypercholesterolemia, diabetes, or TBI of any kind. Some compensation for low educational attainment was possible via a complex occupation later in life. CONCLUSION: Non-genetic factors have a role in YOD, though the relative importance of each factor may be different to late onset dementia. The timing and severity of exposure, as well as the potential for compensation with later protective exposures, are important considerations for potential prevention strategies.
BACKGROUND: Several brain reserve, vascular risk, and other modifiable factors have been associated with late-onset dementia, but their association with young onset dementia (YOD) has not been adequately explored. OBJECTIVE: To examine the association of cognitive reserve enhancing factors, cardiovascular risk factors (including smoking), depression, alcohol use, and traumatic brain injury (TBI) with non-autosomal dominant degenerative and/or vascular YOD. METHODS: Data for this matched case-control study were taken from two larger studies conducted in NSW, Australia. One comprised all people with YOD within a geographical region, while the other exclusively included Aboriginal and Torres Strait Islander participants. Dementia diagnosis was confirmed by clinical consensus, and risk exposure was retrospectively self- and/or informant-reported. RESULTS:Participants were 96 people with YOD (58.4% with probable Alzheimer's disease) and 175 age-group, sex, and sample matched control participants. Poor educational attainment, low participation in cognitive leisure activity, stroke, transient ischemic attack, and self-reported very heavy alcohol use were related to the risk of primary degenerative and/or vascular YOD. The effect of hypertension and depression varied depending on when they occurred relative to dementia onset. Current smoking was significantly associated with risk in univariate analyses but did not retain significance in multivariate modelling. There was no association with hypercholesterolemia, diabetes, or TBI of any kind. Some compensation for low educational attainment was possible via a complex occupation later in life. CONCLUSION: Non-genetic factors have a role in YOD, though the relative importance of each factor may be different to late onset dementia. The timing and severity of exposure, as well as the potential for compensation with later protective exposures, are important considerations for potential prevention strategies.
Entities:
Keywords:
Alzheimer’s disease; Lewy body; early onset dementia; epidemiology; frontotemporal; lifestyle; modifiable; protective; risk; vascular; young onset dementia
Authors: Ji Hee Yu; Kyungdo Han; Sanghyun Park; Hanna Cho; Da Young Lee; Jin Wook Kim; Ji A Seo; Sin Gon Kim; Sei Hyun Baik; Yong Gyu Park; Kyung Mook Choi; Seon Mee Kim; Nan Hee Kim Journal: Diabetes Metab J Date: 2019-11-12 Impact factor: 5.376
Authors: Leah Couzner; Sally Day; Brian Draper; Adrienne Withall; Kate E Laver; Claire Eccleston; Kate-Ellen Elliott; Fran McInerney; Monica Cations Journal: BMC Health Serv Res Date: 2022-01-02 Impact factor: 2.655