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Cited 9 time in webofscience Cited 10 time in scopus
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Dynamic changes of oligomeric amyloid beta levels in plasma induced by spiked synthetic A beta(42)open access

Authors
An, Seong Soo A.Lee, Byoung-subYu, Ji SunLim, KuntaekKim, Gwang JeLee, RyanKim, ShinwonKang, SungminPark, Young HoWang, Min JeongYang, Young SoonYoun, Young ChulKim, SangYun
Issue Date
Oct-2017
Publisher
BIOMED CENTRAL LTD
Keywords
Multimer detection system; Alzheimer's disease; Amyloid-beta; Oligomers; Blood biomarker; Synthetic amyloid-beta; ELISA; Plasma test
Citation
ALZHEIMERS RESEARCH & THERAPY, v.9, no.1
Journal Title
ALZHEIMERS RESEARCH & THERAPY
Volume
9
Number
1
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/3771
DOI
10.1186/s13195-017-0310-6
ISSN
1758-9193
Abstract
Background: A reliable blood-based assay is required to properly diagnose and monitor Alzheimer's disease (AD). Many attempts have been made to develop such a diagnostic tool by measuring amyloid-beta oligomers (A beta Os) in the blood, but none have been successful in terms of method reliability. We present a multimer detection system (MDS), initially developed for the detection of prion oligomers in the blood, to detect A beta Os. Methods: To characterize A beta in the blood, plasma was spiked with synthetic amyloid-beta (A beta) and incubated over time. Then, the MDS was used to monitor the dynamic changes of A beta O levels in the plasma. Results: Increasing concentrations of A beta Os were observed in the plasma of patients with AD but not in the plasma of normal control subjects. The plasma from patients with AD (n = 27) was differentiated from that of the age-matched normal control subjects (n = 144) with a sensitivity of 83.3% and a specificity of 90.0%. Conclusions: Synthetic A beta spiked into the blood plasma of patients with AD, but that of not elderly normal control subjects, induced dynamic changes in the formation of A beta Os over time. A beta Os were detected by the MDS, which is a useful blood-based assay with high sensitivity and specificity for AD diagnosis.
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