Show simple item record

dc.contributor.authorStephan, Blossom C. M.
dc.date.accessioned2024-01-11T15:05:37Z
dc.date.available2024-01-11T15:05:37Z
dc.date.issued2022
dc.identifier.citationStephan, B. C. M., Gaughan, D. M., Edland, S., Gudnason, V., Launer, L. J. & White, L. R. Mid- and later-life risk factors for predicting neuropathological brain changes associated with alzheimer's and vascular dementia: The Honolulu Asia aging study and the age, gene/environment susceptibility-reykjavik study. Alzheimer's and Dementia 19 (5), pp.1705-1713.en_US
dc.identifier.other10.1002/alz.12762
dc.identifier.urihttp://hdl.handle.net/20.500.12904/18073
dc.description© 2022 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
dc.description.abstractAbstract Introduction Dementia prediction models are necessary to inform the development of dementia risk reduction strategies. Here, we examine the utility of neuropathological-based risk scores to predict clinical dementia. Methods Models were developed for predicting Alzheimer's disease (AD) and non-AD neuropathologies using the Honolulu Asia Aging neuropathological sub-study (HAAS; n = 852). Model accuracy for predicting clinical dementia, over 30 years, was tested in the non-autopsied HAAS sample (n = 2960) and the Age, Gene/Environment Susceptibility-Reykjavik Study (n = 4614). Results Different models were identified for predicting neurodegenerative and vascular neuropathology (c-statistic range: 0.62 to 0.72). These typically included age, APOE, and a blood pressure-related measure. The neurofibrillary tangle and micro-vascular lesion models showed good accuracy for predicting clinical vascular dementia. Discussion There may be shared risk factors across dementia-related lesions, suggesting common pathways. Strategies targeting these models may reduce risk or postpone clinical symptoms of dementia as well as reduce neuropathological burden associated with AD and vascular lesions.
dc.description.urihttps://alz-journals.onlinelibrary.wiley.com/doi/abs/10.1002/alz.12762en_US
dc.language.isoenen_US
dc.subjectDementiaen_US
dc.subjectAlzheimer diseaseen_US
dc.titleMid- and later-life risk factors for predicting neuropathological brain changes associated with alzheimer's and vascular dementia: The Honolulu Asia aging study and the age, gene/environment susceptibility-reykjavik studyen_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionNAen_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.dateFOA2024-01-11T15:06:30Z
refterms.panelUnspecifieden_US
refterms.dateFirstOnline2022-10-04
html.description.abstractAbstract Introduction Dementia prediction models are necessary to inform the development of dementia risk reduction strategies. Here, we examine the utility of neuropathological-based risk scores to predict clinical dementia. Methods Models were developed for predicting Alzheimer's disease (AD) and non-AD neuropathologies using the Honolulu Asia Aging neuropathological sub-study (HAAS; n = 852). Model accuracy for predicting clinical dementia, over 30 years, was tested in the non-autopsied HAAS sample (n = 2960) and the Age, Gene/Environment Susceptibility-Reykjavik Study (n = 4614). Results Different models were identified for predicting neurodegenerative and vascular neuropathology (c-statistic range: 0.62 to 0.72). These typically included age, APOE, and a blood pressure-related measure. The neurofibrillary tangle and micro-vascular lesion models showed good accuracy for predicting clinical vascular dementia. Discussion There may be shared risk factors across dementia-related lesions, suggesting common pathways. Strategies targeting these models may reduce risk or postpone clinical symptoms of dementia as well as reduce neuropathological burden associated with AD and vascular lesions.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


Files in this item

Thumbnail
Name:
Stephan 2022 1-9.pdf
Size:
446.1Kb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record