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Cognitive trajectories of patients with focal ss-amyloid deposition

Authors
Kim, Si EunLee, ByungjuJang, HyeminChin, JuheeKhoo, Ching SoongChoe, Yeong SimKim, Ji SunKang, Sung HoonKim, Hang-RaiHwangbo, SongJeong, Jee HyangYoon, Soo JinPark, Kyung WonKim, Eun-JooYoon, BoraJang, Jae-WonHong, Jin YongNa, Duk L.Seo, Sang WonChoi, Seong HyeKim, Hee Jin
Issue Date
19-2월-2021
Publisher
BMC
Keywords
& #223; -Amyloid; F-18-flutemetamol PET; Longitudinal studies; Cognitive decline; Alzheimer& #8217; s disease
Citation
ALZHEIMERS RESEARCH & THERAPY, v.13, no.1
Indexed
SCIE
SCOPUS
Journal Title
ALZHEIMERS RESEARCH & THERAPY
Volume
13
Number
1
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/129182
DOI
10.1186/s13195-021-00787-7
ISSN
1758-9193
Abstract
Background The presence of ss-amyloid (Ass) in the brain can be identified using amyloid PET. In clinical practice, the amyloid PET is interpreted based on dichotomous visual rating, which renders focal Ass accumulation be read as positive for Ass. However, the prognosis of patients with focal Ass deposition is not well established. Thus, we investigated cognitive trajectories of patients with focal Ass deposition. Methods We followed up 240 participants (112 cognitively unimpaired [CU], 78 amnestic mild cognitive impairment [aMCI], and 50 Alzheimer's disease (AD) dementia [ADD]) for 2 years from 9 referral centers in South Korea. Participants were assessed with neuropsychological tests and F-18-flutemetamol (FMM) positron emission tomography (PET). Ten regions (frontal, precuneus/posterior cingulate (PPC), lateral temporal, parietal, and striatum of each hemisphere) were visually examined in the FMM scan, and participants were divided into three groups: No-FMM, Focal-FMM (FMM uptake in 1-9 regions), and Diffuse-FMM. We used mixed-effects model to investigate the speed of cognitive decline in the Focal-FMM group according to the cognitive level, extent, and location of Ass involvement, in comparison with the No- or Diffuse-FMM group. Results Forty-five of 240 (18.8%) individuals were categorized as Focal-FMM. The rate of cognitive decline in the Focal-FMM group was faster than the No-FMM group (especially in the CU and aMCI stage) and slower than the Diffuse-FMM group (in particular in the CU stage). Within the Focal-FMM group, participants with FMM uptake to a larger extent (7-9 regions) showed faster cognitive decline compared to those with uptake to a smaller extent (1-3 or 4-6 regions). The Focal-FMM group was found to have faster cognitive decline in comparison with the No-FMM when there was uptake in the PPC, striatum, and frontal cortex. Conclusions When predicting cognitive decline of patients with focal Ass deposition, the patients' cognitive level, extent, and location of the focal involvement are important.
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