Longitudinal protein changes in blood plasma associated with the rate of cognitive decline in Alzheimer's disease

Sattlecker, Martina, Khondoker, Mizanur ORCID: https://orcid.org/0000-0002-1801-1635, Proitsi, Petroula, Williams, Stephen, Soininen, Hilkka, Kloszewska, Iwona, Mecocci, Patrizia, Tsolaki, Magda, Vellas, Bruno, Lovestone, Simon and Dobson, Richard J. B. and AddNeuroMed Consortium (2016) Longitudinal protein changes in blood plasma associated with the rate of cognitive decline in Alzheimer's disease. Journal of Alzheimer's Disease, 49 (4). pp. 1105-1114. ISSN 1387-2877

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Biomarkers of Alzheimer's disease (AD) progression are needed to support the development of urgently needed disease modifying drugs. We employed a SOMAscan assay for quantifying 1,001 proteins in blood samples from 90 AD subjects, 37 stable mild cognitive impaired (MCI) subjects, 39 MCI subjects converting to AD within a year and 69 controls at baseline and one year follow up. We used linear mixed effects models to identify proteins changing significantly over one year with the rate of cognitive decline, which was quantified as the reduction in Mini Mental State Examination (MMSE) scores. Additionally, we investigated proteins changing differently across disease groups and during the conversion from MCI to AD. We found that levels of proteins belonging to the complement cascade increase significantly in fast declining AD patients. Longitudinal changes in the complement cascade might be a surrogate biomarker for disease progression. We also found that members of the cytokine-cytokine receptor interaction pathway change during AD when compared to healthy aging subjects.

Item Type: Article
Uncontrolled Keywords: alzheimer's disease,cognitive decline,complement cascade,cytokine-cytokine receptor interaction,plasma proteins
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Depositing User: Pure Connector
Date Deposited: 24 Sep 2016 00:24
Last Modified: 24 May 2023 14:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/60031
DOI: 10.3233/JAD-140669

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