Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11706
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dc.contributor.authorRembach, Alan-
dc.contributor.authorFaux, Noel G-
dc.contributor.authorWatt, Andrew D-
dc.contributor.authorPertile, Kelly K-
dc.contributor.authorRumble, Rebecca L-
dc.contributor.authorTrounson, Brett O-
dc.contributor.authorFowler, Christopher J-
dc.contributor.authorRoberts, Blaine R-
dc.contributor.authorPerez, Keyla A-
dc.contributor.authorLi, Qiao-Xin-
dc.contributor.authorLaws, Simon M-
dc.contributor.authorTaddei, Kevin-
dc.contributor.authorRainey-Smith, Stephanie R-
dc.contributor.authorRobertson, Joanne S-
dc.contributor.authorVandijck, Manu-
dc.contributor.authorVanderstichele, Hugo-
dc.contributor.authorBarnham, Kevin J-
dc.contributor.authorEllis, Kathryn A-
dc.contributor.authorSzoeke, Cassandra-
dc.contributor.authorMacaulay, S Lance-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorAmes, David-
dc.contributor.authorMartins, Ralph N-
dc.contributor.authorBush, Ashley I-
dc.contributor.authorMasters, Colin L-
dc.date.accessioned2015-05-16T01:19:27Z
dc.date.available2015-05-16T01:19:27Z
dc.date.issued2013-03-13-
dc.identifier.citationAlzheimer's & Dementia : the Journal of the Alzheimer's Association 2013; 10(1): 53-61en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11706en
dc.description.abstractA practical biomarker is required to facilitate the preclinical diagnosis of Alzheimer's disease (AD).Plasma amyloid beta (Aβ)1-40, Aβ1-42, Aβn-40, and Aβn-42 peptides were measured at baseline and after 18 months in 771 participants from the Australian Imaging Biomarkers and Lifestyle (AIBL) study of aging. Aβ peptide levels were compared with clinical pathology, neuroimaging and neuropsychological measurements.Although inflammatory and renal function covariates influenced plasma Aβ levels significantly, a decrease in Aβ1-42/Aβ1-40 was observed in patients with AD, and was also inversely correlated with neocortical amyloid burden. During the 18 months, plasma Aβ1-42 decreased in subjects with mild cognitive impairment (MCI) and in those transitioning from healthy to MCI.Our findings are consistent with a number of published plasma Aβ studies and, although the prognostic value of individual measures in any given subject is limited, the diagnostic contribution of plasma Aβ may demonstrate utility when combined with a panel of peripheral biomarkers.en
dc.language.isoenen
dc.subject.otherAlzheimer's diseaseen
dc.subject.otherAmyloid-βen
dc.subject.otherBiomarkersen
dc.subject.otherDiagnosisen
dc.subject.otherPittsburgh compound Ben
dc.subject.otherPositron emission tomographyen
dc.subject.otherAgeden
dc.subject.otherAged, 80 and overen
dc.subject.otherAging.blooden
dc.subject.otherAlzheimer Disease.blood.genetics.radionuclide imagingen
dc.subject.otherAmyloid beta-Peptides.blooden
dc.subject.otherApolipoprotein E4.geneticsen
dc.subject.otherChi-Square Distributionen
dc.subject.otherCohort Studiesen
dc.subject.otherDisease Progressionen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherMild Cognitive Impairment.blood.radionuclide imagingen
dc.subject.otherNeuropsychological Testsen
dc.subject.otherPeptide Fragments.blooden
dc.subject.otherPositron-Emission Tomographyen
dc.titleChanges in plasma amyloid beta in a longitudinal study of aging and Alzheimer's disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleAlzheimer's & dementia : the journal of the Alzheimer's Associationen
dc.identifier.affiliationNational Ageing Research Institute, Parkville, Victoria, Australiaen
dc.identifier.affiliationSir James McCusker Alzheimer's Disease Research Unit (Hollywood Private Hospital), Perth, Western Australia, Australiaen
dc.identifier.affiliationDepartment of Diagnostic Development, Innogenetics NV, Ghent, Belgiumen
dc.identifier.affiliationBiomarkable, Gent, Belgium.en
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationCSIRO Molecular and Health Technologies, Parkville, Victoria, Australiaen
dc.identifier.affiliationCentre of Excellence for Alzheimer's Disease Research & Care, School of Medical Sciences, Edith Cowan University, Joondalup. Western Australia, Australiaen
dc.identifier.affiliationDepartment of Psychiatry, St George's Hospital, University of Melbourne, Victoria, Australiaen
dc.identifier.affiliationThe Mental Health Research Institute, The University of Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Diagnostic Development, Innogenetics NV, Ghent, Belgium.en
dc.identifier.doi10.1016/j.jalz.2012.12.006en
dc.description.pages53-61en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23491263en
dc.contributor.corpauthorAIBL research groupen
dc.type.contentTexten
dc.type.austinJournal Articleen
local.name.researcherMasters, Colin L
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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