Sorry, I don't understand your search. ×
Back to Search Start Over

Predicting Symptom Onset in Sporadic Alzheimer Disease With Amyloid PET

Authors :
Brian A. Gordon
Virginia Buckles
William E. Klunk
Anne M. Fagan
Guoqiao Wang
David M. Holtzman
John C. Morris
Tammie L.S. Benzinger
Randall J. Bateman
Suzanne E. Schindler
Yan Li
Chengjie Xiong
Dean W. Coble
Source :
Neurology
Publication Year :
2021
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2021.

Abstract

Background and ObjectivesTo predict when cognitively normal individuals with brain amyloidosis will develop symptoms of Alzheimer disease (AD).MethodsBrain amyloid burden was measured by amyloid PET with Pittsburgh compound B. The mean cortical standardized uptake value ratio (SUVR) was transformed into a timescale with the use of longitudinal data.ResultsAmyloid accumulation was evaluated in 236 individuals who underwent >1 amyloid PET scan. The average age was 66.5 ± 9.2 years, and 12 individuals (5%) had cognitive impairment at their baseline amyloid PET scan. A tipping point in amyloid accumulation was identified at a low level of amyloid burden (SUVR 1.2), after which nearly all individuals accumulated amyloid at a relatively consistent rate until reaching a high level of amyloid burden (SUVR 3.0). The average time between levels of amyloid burden was used to estimate the age at which an individual reached SUVR 1.2. Longitudinal clinical diagnoses for 180 individuals were aligned by the estimated age at SUVR 1.2. In the 22 individuals who progressed from cognitively normal to a typical AD dementia syndrome, the estimated age at which an individual reached SUVR 1.2 predicted the age at symptom onset (R2 = 0.54, p < 0.0001, root mean square error [RMSE] 4.5 years); the model was more accurate after exclusion of 3 likely misdiagnoses (R2 = 0.84, p < 0.0001, RMSE 2.8 years).ConclusionThe age at symptom onset in sporadic AD is strongly correlated with the age at which an individual reaches a tipping point in amyloid accumulation.

Details

ISSN :
1526632X and 00283878
Volume :
97
Database :
OpenAIRE
Journal :
Neurology
Accession number :
edsair.doi.dedup.....d513d3c8efb9f5af7f943697dc1ea32e