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dc.contributor.authorLeung, R
dc.contributor.authorProitsi, P
dc.contributor.authorSimmons, A
dc.contributor.authorLunnon, Katie
dc.contributor.authorGüntert, A
dc.contributor.authorKronenberg, D
dc.contributor.authorPritchard, M
dc.contributor.authorTsolaki, M
dc.contributor.authorMecocci, P
dc.contributor.authorKloszewska, I
dc.contributor.authorVellas, B
dc.contributor.authorSoininen, H
dc.contributor.authorWahlund, LO
dc.contributor.authorLovestone, Simon
dc.date.accessioned2016-02-11T10:09:37Z
dc.date.issued2013-06-10
dc.description.abstractMarkers 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.sponsorshipNational 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 Londonen_GB
dc.description.sponsorshipEuropean Union of the Sixth Framework programen_GB
dc.identifier.citationPLoS One, 2013, Vol. 8 (6), e64971en_GB
dc.identifier.doi10.1371/journal.pone.0064971
dc.identifier.grantnumberFP6-2004-LIFESCIHEALTH-5en_GB
dc.identifier.otherPONE-D-12-20777
dc.identifier.urihttp://hdl.handle.net/10871/19700
dc.language.isoenen_GB
dc.publisherPublic Library of Scienceen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/23762274en_GB
dc.relation.urlhttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0064971en_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.subjectAgeden_GB
dc.subjectAlzheimer Diseaseen_GB
dc.subjectAtrophyen_GB
dc.subjectBiomarkersen_GB
dc.subjectBrainen_GB
dc.subjectCase-Control Studiesen_GB
dc.subjectCognition Disordersen_GB
dc.subjectCohort Studiesen_GB
dc.subjectCytokinesen_GB
dc.subjectDisease Progressionen_GB
dc.subjectEnzyme-Linked Immunosorbent Assayen_GB
dc.subjectFemaleen_GB
dc.subjectFunctional Neuroimagingen_GB
dc.subjectHumansen_GB
dc.subjectInflammation Mediatorsen_GB
dc.subjectMagnetic Resonance Imagingen_GB
dc.subjectMaleen_GB
dc.subjectPrognosisen_GB
dc.subjectSeverity of Illness Indexen_GB
dc.titleInflammatory proteins in plasma are associated with severity of Alzheimer's disease.en_GB
dc.typeArticleen_GB
dc.date.available2016-02-11T10:09:37Z
dc.identifier.issn1932-6203
exeter.place-of-publicationUnited States
dc.descriptionPublished onlineen_GB
dc.descriptionComparative Studyen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.descriptionThis 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.journalPLoS Oneen_GB


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