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Relationship Between Amyloid-β Positivity and Progression to Mild Cognitive Impairment or Dementia over 8 Years in Cognitively Normal Older Adults.
- Source :
-
Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2018; Vol. 65 (4), pp. 1313-1325. - Publication Year :
- 2018
-
Abstract
- Background: Preclinical Alzheimer's disease (AD) is defined by cerebral amyloid-β positivity (Aβ+) in cognitively normal (CN) older adults.<br />Objective: To estimate the risk of progression to the symptomatic stages of AD due to PET Aβ+ and the extent that progression was influenced by other demographic, genetic, and clinical characteristics in a large prospective study.<br />Methods: Fine-Gray subdistribution modeling was used to examine the risk of progression from CN to MCI/dementia due to Aβ+, APOEɛ4 carriage, and their interaction in the Australian Imaging, Biomarkers and Lifestyle (AIBL) flagship study of aging CN cohort (n = 599) over 8 years.<br />Results: 17.7% Aβ+ and 8.1% Aβ-progressed over 8 years (OR: 2.43). Risk of progression for Aβ+ was 65-104% greater than Aβ-. Aβ+ APOEɛ4 carriers were at 348% greater risk than all other participants. Significant risk factors of progression in Aβ+ were age (HR: 1.05), PET SUVR (HR: 2.49) and APOE ɛ4 carriage (HR: 2.63); only age was a significant risk factor in Aβ-(HR: 1.09). Aβ-progressors were not near the threshold for Aβ+. These relationships were not moderated by hypertension, diabetes, obesity, or stroke/TIA.<br />Conclusion: Aβ+ is an important prognostic marker for progression from CN to MCI/dementia in older adults and APOEɛ4 carriage provides further predictive value in the presence of Aβ+. These data suggest that Aβ-associated clinical progression is consistent with clinical-pathological models of AD, whereas progression in the absence of elevated Aβ deposition may be the result of neuropathological processes other than AD that accumulate with age.
- Subjects :
- Aged
Aged, 80 and over
Apolipoprotein E4 genetics
Cerebral Cortex diagnostic imaging
Cognitive Dysfunction diagnostic imaging
Cognitive Dysfunction genetics
Dementia diagnostic imaging
Dementia genetics
Female
Humans
Longitudinal Studies
Male
Middle Aged
Positron-Emission Tomography
Statistics, Nonparametric
Survival Analysis
Aging pathology
Amyloid beta-Peptides metabolism
Cerebral Cortex metabolism
Cognitive Dysfunction pathology
Dementia pathology
Disease Progression
Subjects
Details
- Language :
- English
- ISSN :
- 1875-8908
- Volume :
- 65
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of Alzheimer's disease : JAD
- Publication Type :
- Academic Journal
- Accession number :
- 30149452
- Full Text :
- https://doi.org/10.3233/JAD-180507