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https://ahro.austin.org.au/austinjspui/handle/1/16045
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DC Field | Value | Language |
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dc.contributor.author | Lim, YY | - |
dc.contributor.author | Snyder, PJ | - |
dc.contributor.author | Pietrzak, RH | - |
dc.contributor.author | Ukigi, A | - |
dc.contributor.author | Villemagne, Victor L | - |
dc.contributor.author | Ames, David | - |
dc.contributor.author | Salvado, O | - |
dc.contributor.author | Bourgeat, P | - |
dc.contributor.author | Martins, Ralph N | - |
dc.contributor.author | Masters, Colin L | - |
dc.contributor.author | Rowe, Christopher C | - |
dc.contributor.author | Maruff, Paul | - |
dc.date.accessioned | 2016-06-20T05:07:08Z | - |
dc.date.available | 2016-06-20T05:07:08Z | - |
dc.date.issued | 2015-12-12 | - |
dc.identifier.citation | Alzheimer's & Dementia (Amst) 2016; 2: 19-26 | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/16045 | - |
dc.description.abstract | INTRODUCTION: Cognitive composite scores developed for preclinical Alzheimer's disease (AD) often consist of multiple cognitive domains as they may provide greater sensitivity to detect β-amyloid (Aβ)-related cognitive decline than episodic memory (EM) composite scores alone. However, this has never been empirically tested. We compared the rate of cognitive decline associated with high Aβ (Aβ+) and very high Aβ (Aβ++) in cognitively normal (CN) older adults on three multidomain cognitive composite scores and one single-domain (EM) composite score. METHODS: CN older adults (n = 423) underwent Aβ neuroimaging and completed neuropsychological assessments at baseline, and at 18-, 36-, 54-, and 72-month follow-ups. Four cognitive composite scores were computed: the ADCS-PACC (ADCS-Preclinical Alzheimer Cognitive Composite), ADCS-PACC without the inclusion of the mini-mental state examination (MMSE), an EM composite, and the Z-scores of Attention, Verbal fluency, and Episodic memory for Nondemented older adults (ZAVEN) composite. RESULTS: Compared with Aβ+ CN older adults, Aβ++ CN older adults showed faster rates of decline across all cognitive composites, with the largest decline observed for ZAVEN composite (d = 1.07). Similarly, compared with Aβ- CN older adults, Aβ+ CN older adults also showed faster rates of cognitive decline, but only for the ADCS-PACC no MMSE (d = 0.43), EM (d = 0.53), and ZAVEN (d = 0.50) composites. DISCUSSION: Aβ-related cognitive decline is best detected using validated neuropsychological instruments. Removal of the MMSE from the ADCS-PACC and replacing it with a test of executive function (verbal fluency; i.e., the ZAVEN) rendered this composite more sensitive even in detecting Aβ-related cognitive decline between Aβ+ and Aβ++ CN older adults. | en |
dc.subject | Amyloid | en |
dc.subject | Cognitive composite | en |
dc.subject | Cognitive decline | en |
dc.subject | Neuropsychological assessment | en |
dc.subject | Preclinical Alzheimer's disease | en |
dc.title | Sensitivity of composite scores to amyloid burden in preclinical Alzheimer's disease: introducing the Z-scores of attention, verbal fluency, and episodic memory for nondemented older adults composite score | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Alzheimer's & Dementia (Amsterdam, Netherlands) | en |
dc.identifier.affiliation | Commonwealth Scientific Industrial Research Organization (CSIRO) Preventative Health National Research Flagship, Australian e-Health Research Centre-BioMedIA, Brisbane, Queensland, Australia | en |
dc.identifier.affiliation | Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA | en |
dc.identifier.affiliation | Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | Centre of Excellence for Alzheimer's Disease Research and Care, Edith Cowan University, Joondalup, Western Australia, Australia | en |
dc.identifier.affiliation | Cogstate Ltd., Melbourne, Victoria, Australia | en |
dc.identifier.affiliation | National Ageing Research Institute, Parkville, Victoria, Australia | en |
dc.identifier.affiliation | The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria, Australia | en |
dc.identifier.affiliation | Department of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | Academic Unit for Psychiatry of Old Age, St. Vincent's Health, The University of Melbourne, Kew, Victoria, Australia | en |
dc.identifier.affiliation | Department of Neurology, Warren Alpert School of Medicine, Brown University, Providence, RI, USA; Interdisciplinary Neuroscience Program, University of Rhode Island, Kingston, RI, USA | en |
dc.identifier.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/27239532 | en |
dc.identifier.doi | 10.1016/j.dadm.2015.11.003 | en |
dc.type.content | Text | en |
dc.type.austin | Journal Article | en_US |
local.name.researcher | Masters, Colin L | |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Molecular Imaging and Therapy | - |
crisitem.author.dept | The Florey Institute of Neuroscience and Mental Health | - |
crisitem.author.dept | Molecular Imaging and Therapy | - |
Appears in Collections: | Journal articles |
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