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

Author:

Shim Kyu Hwan1,Kim Danyeong1,Kang Min Ju2,Pyun Jung‐Min3,Park Young Ho4,Youn Young Chul5,Park Kyung Won6,Suk Kyoungho7,Lee Ho‐Won8,Gomes Bárbara Fernandes9,Zetterberg Henrik910111213,An Seong Soo A.1ORCID,Kim SangYun4,

Affiliation:

1. Department of Bionano Technology Gachon University Seongnam Republic of Korea

2. Department of Neurology Veterans Medical Research Institute Veterans Health Service Medical Center Seoul Republic of Korea

3. Department of Neurology Soonchunhyang University Seoul Hospital Soonchunhyang University College of Medicine Seoul Republic of Korea

4. Department of Neurology Seoul National University College of Medicine and Clinical Neuroscience Center Seoul National University Bundang Hospital Seongnam Republic of Korea

5. Department of Neurology Chung‐Ang University College of Medicine Seoul Republic of Korea

6. Department of Neurology Dong‐A University College of Medicine and Institute of Convergence Bio‐Health Busan Republic of Korea

7. Department of Pharmacology Kyungpook National University School of Medicine Daegu Republic of Korea

8. Department of Neurology Kyungpook National University School of Medicine Daegu Republic of Korea

9. Department of Psychiatry and Neurochemistry Institute of Neuroscience & Physiology the Sahlgrenska Academy at the University of Gothenburg Mölndal Sweden

10. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

11. Department of Neurodegenerative Disease UCL Institute of Neurology, Queen Square London UK

12. UK Dementia Research Institute at UCL London UK

13. Hong Kong Center for Neurodegenerative Diseases, Clear Water Bay Hong Kong China

Abstract

AbstractINTRODUCTIONAlzheimer'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.METHODSPlasma 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.RESULTSPlasma 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.DISCUSSIONIncreased 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.

Publisher

Wiley

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