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dc.contributor.authorHye, Aen_US
dc.contributor.authorRiddoch-Contreras, Jen_US
dc.contributor.authorBaird, ALen_US
dc.contributor.authorAshton, NJen_US
dc.contributor.authorBazenet, Cen_US
dc.contributor.authorLeung, Ren_US
dc.contributor.authorWestman, Een_US
dc.contributor.authorSimmons, Aen_US
dc.contributor.authorDobson, Ren_US
dc.contributor.authorSattlecker, Men_US
dc.contributor.authorLupton, Men_US
dc.contributor.authorLunnon, Ken_US
dc.contributor.authorKeohane, Aen_US
dc.contributor.authorWard, Men_US
dc.contributor.authorPike, Ien_US
dc.contributor.authorZucht, HDen_US
dc.contributor.authorPepin, Den_US
dc.contributor.authorZheng, Wen_US
dc.contributor.authorTunnicliffe, Aen_US
dc.contributor.authorRichardson, Jen_US
dc.contributor.authorGauthier, Sen_US
dc.contributor.authorSoininen, Hen_US
dc.contributor.authorKłoszewska, Ien_US
dc.contributor.authorMecocci, Pen_US
dc.contributor.authorTsolaki, Men_US
dc.contributor.authorVellas, Ben_US
dc.contributor.authorLovestone, Sen_US
dc.date.accessioned2015-09-22T10:14:57Z
dc.date.available2014-05-12en_US
dc.date.issued2014-11en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/8805
dc.description.abstractBACKGROUND: The study aimed to validate previously discovered plasma biomarkers associated with AD, using a design based on imaging measures as surrogate for disease severity and assess their prognostic value in predicting conversion to dementia. METHODS: Three multicenter cohorts of cognitively healthy elderly, mild cognitive impairment (MCI), and AD participants with standardized clinical assessments and structural neuroimaging measures were used. Twenty-six candidate proteins were quantified in 1148 subjects using multiplex (xMAP) assays. RESULTS: Sixteen proteins correlated with disease severity and cognitive decline. Strongest associations were in the MCI group with a panel of 10 proteins predicting progression to AD (accuracy 87%, sensitivity 85%, and specificity 88%). CONCLUSIONS: We have identified 10 plasma proteins strongly associated with disease severity and disease progression. Such markers may be useful for patient selection for clinical trials and assessment of patients with predisease subjective memory complaints.en_US
dc.description.sponsorshipMedical Research Council (MRC) UK (G0801464), Alzheimer's Research UK (ARUK), The National Institute for Health Research (NIHR) Biomedical Research Centre, Biomedical Research Unit for Dementia, and to AddNeuroMed through the EU FP6 program. The research leading to these results has received support from the Innovative Medicines Initiative Joint Undertaking under EMIF grant agreement n° 115372, resources of which are composed of financial contribution from the European Union's Seventh Framework Programme (FP7/2007-2013) and EFPIA companies' in kind contributionen_US
dc.format.extent799 - 807.e2en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofAlzheimers Dementen_US
dc.subjectAlzheimer's diseaseen_US
dc.subjectBiomarkeren_US
dc.subjectMild cognitive impairmenten_US
dc.subjectPathologyen_US
dc.subjectPlasmaen_US
dc.subjectPrediction and magnetic resonance imagingen_US
dc.subjectAgeden_US
dc.subjectAged, 80 and overen_US
dc.subjectApolipoproteins Een_US
dc.subjectBlood Proteinsen_US
dc.subjectCognitive Dysfunctionen_US
dc.subjectCohort Studiesen_US
dc.subjectDementiaen_US
dc.subjectDisease Progressionen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectImmunoassayen_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectMaleen_US
dc.subjectMental Status Scheduleen_US
dc.subjectPredictive Value of Testsen_US
dc.subjectProdromal Symptomsen_US
dc.subjectROC Curveen_US
dc.subjectStatistics as Topicen_US
dc.titlePlasma proteins predict conversion to dementia from prodromal disease.en_US
dc.typeArticle
dc.identifier.doi10.1016/j.jalz.2014.05.1749en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/25012867en_US
pubs.issue6en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublisheden_US
pubs.volume10en_US
dcterms.dateAccepted2014-05-12en_US


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