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Prognostic plasma protein panel for A beta deposition in the brain in Alzheimer's disease

Authors
Park, Jong-ChanHan, Sun-HoLee, HangyeoreJeong, HyobinByun, Min SooBae, JingiKim, HokeunLee, Dong YoungYi, DahyunShin, Seong A.Kim, Yu KyeongHwang, DaeheeLee, Sang-WonMook-Jung, Inhee
Issue Date
12월-2019
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
TMT; Cerebral amyloid deposition; Alzheimer' s disease; Proteomics; PiB-PET; Plasma biomarker
Citation
PROGRESS IN NEUROBIOLOGY, v.183
Indexed
SCIE
SCOPUS
Journal Title
PROGRESS IN NEUROBIOLOGY
Volume
183
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/61395
DOI
10.1016/j.pneurobio.2019.101690
ISSN
0301-0082
Abstract
Alzheimer's disease (AD) is the most common age-associated dementia. Many studies have sought to predict cerebral amyloid deposition, the major pathological hallmark of AD, using body fluids such as blood or cerebral spinal fluid (CSF). The use of blood in diagnostic procedures is widespread in medicine; however, existing blood biomarkers for AD remain unreliable. We sought to discover blood biomarkers that discriminate A beta deposition status in the brain. This study used 107 individuals who were cognitively normal (CN), 107 patients with mild cognitive impairment (MCI), and 40 AD patients with Pittsburg compound B positron emission tomography (PiB-PET) amyloid imaging data available. We found five plasma biomarker candidates via mass spectrometry (MS) based-proteomic analysis and validated these proteins using enzyme-linked immunosorbent assay (ELISA). Our integrated models were highly predictive of brain amyloid deposition, exhibiting 0.871 accuracy with 79% sensitivity and 84% specificity overall, and 0.836 accuracy with 68% sensitivity and 90% specificity in patients with MCI. These results indicated that a combination of proteomic-based blood proteins might be a possible biomarker set for predicting cerebral amyloid deposition.
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