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Subsequent correlated changes in complement component 3 and amyloid beta oligomers in the blood of patients with Alzheimer's diseaseopen access

Authors
Shim, Kyu HwanKim, DanyeongKang, Min JuPyun, Jung-MinPark, Young HoYoun, Young ChulPark, Kyung WonSuk, KyounghoLee, Ho-WonGomes, Bárbara FernandesZetterberg, HenrikAn, Seong Soo A.Kim, SangYun
Issue Date
Apr-2024
Publisher
John Wiley and Sons Inc
Keywords
Alzheimer's disease; amyloid beta; biomarker; complement component 3; oligomer; plasma
Citation
Alzheimer's and Dementia, v.20, no.4, pp 2731 - 2741
Pages
11
Journal Title
Alzheimer's and Dementia
Volume
20
Number
4
Start Page
2731
End Page
2741
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/73015
DOI
10.1002/alz.13734
ISSN
1552-5260
1552-5279
Abstract
INTRODUCTION: Alzheimer's disease (AD) involves the complement cascade, with complement component 3 (C3) playing a key role. However, the relationship between C3 and amyloid beta (Aβ) in blood is limited. METHODS: Plasma C3 and Aβ oligomerization tendency (AβOt) were measured in 35 AD patients and 62 healthy controls. Correlations with cerebrospinal fluid (CSF) biomarkers, cognitive impairment, and amyloid positron emission tomography (PET) were analyzed. Differences between biomarkers were compared in groups classified by concordances of biomarkers. RESULTS: Plasma C3 and AβOt were elevated in AD patients and in CSF or amyloid PET–positive groups. Weak positive correlation was found between C3 and AβOt, while both had strong negative correlations with CSF Aβ42 and cognitive performance. Abnormalities were observed for AβOt and CSF Aβ42 followed by C3 changes. DISCUSSION: Increased plasma C3 in AD are associated with amyloid pathology, possibly reflecting a defense response for Aβ clearance. Further studies on Aβ-binding proteins will enhance understanding of Aβ mechanisms in blood. © 2024 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
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