dc.contributor.author | Leung, R | |
dc.contributor.author | Proitsi, P | |
dc.contributor.author | Simmons, A | |
dc.contributor.author | Lunnon, Katie | |
dc.contributor.author | Güntert, A | |
dc.contributor.author | Kronenberg, D | |
dc.contributor.author | Pritchard, M | |
dc.contributor.author | Tsolaki, M | |
dc.contributor.author | Mecocci, P | |
dc.contributor.author | Kloszewska, I | |
dc.contributor.author | Vellas, B | |
dc.contributor.author | Soininen, H | |
dc.contributor.author | Wahlund, LO | |
dc.contributor.author | Lovestone, Simon | |
dc.date.accessioned | 2016-02-11T10:09:37Z | |
dc.date.issued | 2013-06-10 | |
dc.description.abstract | Markers of Alzheimer's disease (AD) are being widely sought with a number of studies suggesting blood measures of inflammatory proteins as putative biomarkers. Here we report findings from a panel of 27 cytokines and related proteins in over 350 subjects with AD, subjects with Mild Cognitive Impairment (MCI) and elderly normal controls where we also have measures of longitudinal change in cognition and baseline neuroimaging measures of atrophy. In this study, we identify five inflammatory proteins associated with evidence of atrophy on MR imaging data particularly in whole brain, ventricular and entorhinal cortex measures. In addition, we observed six analytes that showed significant change (over a period of one year) in people with fast cognitive decline compared to those with intermediate and slow decline. One of these (IL-10) was also associated with brain atrophy in AD. In conclusion, IL-10 was associated with both clinical and imaging evidence of severity of disease and might therefore have potential to act as biomarker of disease progression. | en_GB |
dc.description.sponsorship | National Institute for Health Research (NIHR) Mental Health Biomedical Research Centre and
Dementia Biomedical Research Unit at South London and Maudsley NHS Foundation Trust and King’s College London | en_GB |
dc.description.sponsorship | European Union of the Sixth Framework program | en_GB |
dc.identifier.citation | PLoS One, 2013, Vol. 8 (6), e64971 | en_GB |
dc.identifier.doi | 10.1371/journal.pone.0064971 | |
dc.identifier.grantnumber | FP6-2004-LIFESCIHEALTH-5 | en_GB |
dc.identifier.other | PONE-D-12-20777 | |
dc.identifier.uri | http://hdl.handle.net/10871/19700 | |
dc.language.iso | en | en_GB |
dc.publisher | Public Library of Science | en_GB |
dc.relation.url | http://www.ncbi.nlm.nih.gov/pubmed/23762274 | en_GB |
dc.relation.url | http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0064971 | en_GB |
dc.rights | © 2013 Leung et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en_GB |
dc.subject | Aged | en_GB |
dc.subject | Alzheimer Disease | en_GB |
dc.subject | Atrophy | en_GB |
dc.subject | Biomarkers | en_GB |
dc.subject | Brain | en_GB |
dc.subject | Case-Control Studies | en_GB |
dc.subject | Cognition Disorders | en_GB |
dc.subject | Cohort Studies | en_GB |
dc.subject | Cytokines | en_GB |
dc.subject | Disease Progression | en_GB |
dc.subject | Enzyme-Linked Immunosorbent Assay | en_GB |
dc.subject | Female | en_GB |
dc.subject | Functional Neuroimaging | en_GB |
dc.subject | Humans | en_GB |
dc.subject | Inflammation Mediators | en_GB |
dc.subject | Magnetic Resonance Imaging | en_GB |
dc.subject | Male | en_GB |
dc.subject | Prognosis | en_GB |
dc.subject | Severity of Illness Index | en_GB |
dc.title | Inflammatory proteins in plasma are associated with severity of Alzheimer's disease. | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2016-02-11T10:09:37Z | |
dc.identifier.issn | 1932-6203 | |
exeter.place-of-publication | United States | |
dc.description | Published online | en_GB |
dc.description | Comparative Study | en_GB |
dc.description | Research Support, Non-U.S. Gov't | en_GB |
dc.description | This is a freely-available open access publication. Please cite the published version which is available via the DOI link in this record. | en_GB |
dc.identifier.journal | PLoS One | en_GB |