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dc.contributor.authorLunnon, Katie
dc.contributor.authorSattlecker, M
dc.contributor.authorFurney, SJ
dc.contributor.authorCoppola, G
dc.contributor.authorSimmons, A
dc.contributor.authorProitsi, P
dc.contributor.authorLupton, MK
dc.contributor.authorLourdusamy, A
dc.contributor.authorJohnston, C
dc.contributor.authorSoininen, H
dc.contributor.authorKłoszewska, I
dc.contributor.authorMecocci, P
dc.contributor.authorTsolaki, M
dc.contributor.authorVellas, B
dc.contributor.authorGeschwind, D
dc.contributor.authorLovestone, Simon
dc.contributor.authorDobson, R
dc.contributor.authorHodges, A
dc.date.accessioned2016-02-11T13:46:47Z
dc.date.issued2013-01-10
dc.description.abstractA marker of Alzheimer's disease (AD) that can accurately diagnose disease at the earliest stage would significantly support efforts to develop treatments for early intervention. We have sought to determine the sensitivity and specificity of peripheral blood gene expression as a diagnostic marker of AD using data generated on HT-12v3 BeadChips. We first developed an AD diagnostic classifier in a training cohort of 78 AD and 78 control blood samples and then tested its performance in a validation group of 26 AD and 26 control and 118 mild cognitive impairment (MCI) subjects who were likely to have an AD-endpoint. A 48 gene classifier achieved an accuracy of 75% in the AD and control validation group. Comparisons were made with a classifier developed using structural MRI measures, where both measures were available in the same individuals. In AD and control subjects, the gene expression classifier achieved an accuracy of 70% compared to 85% using MRI. Bootstrapping validation produced expression and MRI classifiers with mean accuracies of 76% and 82%, respectively, demonstrating better concordance between these two classifiers than achieved in a single validation population. We conclude there is potential for blood expression to be a marker for AD. The classifier also predicts a large number of people with MCI, who are likely to develop AD, are more AD-like than normal with 76% of subjects classified as AD rather than control. Many of these people do not have overt brain atrophy, which is known to emerge around the time of AD diagnosis, suggesting the expression classifier may detect AD earlier in the prodromal phase. However, we accept these results could also represent a marker of diseases sharing common etiology.en_GB
dc.description.sponsorshipInnoMed, European Union of the Sixth Framework programen_GB
dc.description.sponsorshipAlzheimer’s Research UKen_GB
dc.description.sponsorshipJohn and Lucille van Geest Foundationen_GB
dc.description.sponsorshipNIHRen_GB
dc.description.sponsorshipBiomedical Research Centre for Mental Health, South London and Maudsley NHS Foundation Trusten_GB
dc.description.sponsorshipInstitute of Psychiatry Kings College Londonen_GB
dc.description.sponsorshipNIA/NIH RC1en_GB
dc.identifier.citationVol. 33, No. 3, pp. 737 - 753en_GB
dc.identifier.doi10.3233/JAD-2012-121363
dc.identifier.grantnumberFP6-2004-LIFESCIHEALTH-5en_GB
dc.identifier.grantnumber1RC1AG035610en_GB
dc.identifier.urihttp://hdl.handle.net/10871/19721
dc.language.isoenen_GB
dc.publisherIOS Pressen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/23042217en_GB
dc.rightsCopyright © 2013 – IOS Press and the authors. All rights reserved. This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License.en_GB
dc.subjectAgeden_GB
dc.subjectAged, 80 and overen_GB
dc.subjectAlzheimer Diseaseen_GB
dc.subjectApolipoproteins Een_GB
dc.subjectBlood Proteinsen_GB
dc.subjectCognition Disordersen_GB
dc.subjectFemaleen_GB
dc.subjectGene Expression Profilingen_GB
dc.subjectHumansen_GB
dc.subjectMagnetic Resonance Imagingen_GB
dc.subjectMaleen_GB
dc.subjectMiddle Ageden_GB
dc.subjectOligonucleotide Array Sequence Analysisen_GB
dc.subjectPredictive Value of Testsen_GB
dc.subjectPsychiatric Status Rating Scalesen_GB
dc.subjectRetrospective Studiesen_GB
dc.subjectSensitivity and Specificityen_GB
dc.titleA blood gene expression marker of early Alzheimer's disease.en_GB
dc.typeArticleen_GB
dc.date.available2016-02-11T13:46:47Z
dc.identifier.issn1387-2877
exeter.place-of-publicationNetherlands
dc.identifier.eissn1875-8908
dc.identifier.journalJournal of Alzheimer's Diseaseen_GB


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