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Application of an amyloid and tau classification system in subcortical vascular cognitive impairment patients

Authors
Jang, HyeminKim, Hee JinPark, SeongbeomPark, Yu HyunChoe, Yeongsim)Cho, HannaLyoo, Chul HyoungYoon, UicheulLee, Jin SanKim, YeshinKim, Seung JooKim, Jun PyoJung, Young HeeRyu, Young HoonChoi, Jae YongMoon, Seung HwanSeong, Joon-KyungDeCarli, CharlesWeiner, Michael W.Lockhart, Samuel N.Cho, Soo HyunNa, Duk L.Seo, Sang Won
Issue Date
Feb-2020
Publisher
SPRINGER
Keywords
Amyloid-beta; TauClassification; Subcortical vascular cognitive impairment; Longitudinal changes
Citation
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, v.47, no.2, pp.292 - 303
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
Volume
47
Number
2
Start Page
292
End Page
303
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189935
DOI
10.1007/s00259-019-04498-y
ISSN
1619-7070
Abstract
Objective To apply an AT (A beta/tau) classification system to subcortical vascular cognitive impairment (SVCI) patients following recently developed biomarker-based criteria of Alzheimer's disease (AD), and to investigate its clinical significance. Methods We recruited 60 SVCI patients who underwent the neuropsychological tests, brain MRI, and F-18-florbetaben and F-18-AV1451 PET at baseline. As a control group, we further recruited 27 patients with AD cognitive impairment (ADCI; eight A beta PET-positive AD dementia and 19 amnestic mild cognitive impairment). ADCI and SVCI patients were classified as having normal or abnormal A beta (A-/A+) and tau (T-/T+) based on PET results. Across the three SVCI groups (A-, A+T-, and A+T+SVCI), we compared longitudinal changes in cognition, hippocampal volume (HV), and cortical thickness using linear mixed models. Results Among SVCI patients, 33 (55%), 20 (33.3%), and seven (11.7%) patients were A-, A+T-, and A+T+, respectively. The frequency of T+ was lower in A+SVCI (7/27, 25.9%) than in A+ADCI (14/20, 70.0%, p = 0.003) which suggested that cerebral small vessel disease affected cognitive impairments independently of A+. A+T-SVCI had steeper cognitive decline than A-SVCI. A+T+SVCI also showed steeper cognitive decline than A+T-SVCI. Also, A+T-SVCI had steeper decrease in HV than A-SVCI, while cortical thinning did not differ between the two groups. A+T+SVCI had greater global cortical thinning compared with A+T-SVCI, while declines in HV did not differ between the two groups. Conclusion This study showed that the AT system successfully characterized SVCI patients, suggesting that the AT system may be usefully applied in a research framework for clinically diagnosed SVCI.
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