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Cortical atrophy pattern-based subtyping predicts prognosis of amnestic MCI: an individual-level analysis

Authors
Kim, Hee JinPark, Jong-YunSeo, Sang WonJung, Young HeeKim, YeshinJang, HyeminKim, Sung TaeSeong, Joon-KyungNa, Duk L
Issue Date
Feb-2019
Publisher
ELSEVIER SCIENCE INC
Keywords
Mild cognitive impairment; Alzheimer' s disease; Cortical atrophy pattern; Classifier
Citation
NEUROBIOLOGY OF AGING, v.74, pp.38 - 45
Indexed
SCIE
SCOPUS
Journal Title
NEUROBIOLOGY OF AGING
Volume
74
Start Page
38
End Page
45
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189478
DOI
10.1016/j.neurobiolaging.2018.10.010
ISSN
0197-4580
Abstract
We categorized patients with amnestic mild cognitive impairment (aMCI) based on cortical atrophy patterns and evaluated whether the prognosis differed across the subtypes. Furthermore, we developed a classifier that learns the cortical atrophy pattern and predicts subtypes at an individual level. A total of 662 patients with aMCI were clustered into 3 subtypes based on cortical atrophy patterns. Of these, 467 patients were followed up for more than 12 months, and the median follow-up duration was 43 months. To predict individual-level subtype, we used a machine learning-based classifier with a 10-fold cross-validation scheme. Patients with aMCI were clustered into 3 subtypes: medial temporal atrophy, minimal atrophy (Min), and parietotemporal atrophy (PT) subtypes. The PT subtype had higher prevalence of APOE epsilon 4 carriers, amyloid PET positivity, and greater risk of dementia conversion than the Min subtype. The accuracy for binary classification was 89.3% (MT vs. Rest), 92.6% (PT vs. Rest), and 86.6% (Min vs. Rest). When we used ensemble model of 3 binary classifiers, the accuracy for predicting the aMCI subtype at an individual level was 89.6%. Patients with aMCI with the PT subtype were more likely to have underlying Alzheimer's disease pathology and showed the worst prognosis. Our classifier may be useful for predicting the prognosis of individual aMCI patients. (C) 2018 Elsevier Inc. All rights reserved.
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