Association of β-Amyloid Level, Clinical Progression, and Longitudinal Cognitive Change in Normal Older Individuals.
Aged
Aged, 80 and over
Amyloid beta-Peptides
/ metabolism
Atrophy
Australia
Brain
/ diagnostic imaging
Cognition
Cognitive Dysfunction
/ diagnostic imaging
Dementia
/ diagnostic imaging
Disease Progression
Female
Healthy Volunteers
Hippocampus
/ diagnostic imaging
Humans
Kaplan-Meier Estimate
Linear Models
Longitudinal Studies
Magnetic Resonance Imaging
Male
Middle Aged
Positron-Emission Tomography
Proportional Hazards Models
Risk Assessment
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
02 02 2021
02 02 2021
Historique:
received:
13
08
2019
accepted:
24
09
2020
pubmed:
14
11
2020
medline:
23
2
2021
entrez:
13
11
2020
Statut:
ppublish
Résumé
To determine the effect of β-amyloid (Aβ) level on progression risk to mild cognitive impairment (MCI) or dementia and longitudinal cognitive change in cognitively normal (CN) older individuals. All CN from the Australian Imaging Biomarkers and Lifestyle study with Aβ PET and ≥3 years follow-up were included (n = 534; age 72 ± 6 years; 27% Aβ positive; follow-up 5.3 ± 1.7 years). Aβ level was divided using the standardized 0-100 Centiloid scale: <15 CL negative, 15-25 CL uncertain, 26-50 CL moderate, 51-100 CL high, >100 CL very high, noting >25 CL approximates a positive scan. Cox proportional hazards analysis and linear mixed effect models were used to assess risk of progression and cognitive decline. Aβ levels in 63% were negative, 10% uncertain, 10% moderate, 14% high, and 3% very high. Fifty-seven (11%) progressed to MCI or dementia. Compared to negative Aβ, the hazard ratio for progression for moderate Aβ was 3.2 (95% confidence interval [CI] 1.3-7.6; The risk of MCI or dementia over 5 years in older CN is related to Aβ level on PET, 5% if negative vs 25% if positive but ranging from 12% if 26-50 CL to 28% if 51-100 CL and 50% if >100 CL. This information may be useful for dementia risk counseling and aid design of preclinical AD trials.
Identifiants
pubmed: 33184233
pii: WNL.0000000000011222
doi: 10.1212/WNL.0000000000011222
pmc: PMC7884996
doi:
Substances chimiques
Amyloid beta-Peptides
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e662-e670Informations de copyright
Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
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