Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16218
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dc.contributor.authorBurnham, Samantha C-
dc.contributor.authorRaghavan, Nandini-
dc.contributor.authorWilson, William-
dc.contributor.authorBaker, David-
dc.contributor.authorRopacki, Michael T-
dc.contributor.authorNovak, Gerald-
dc.contributor.authorAmes, David-
dc.contributor.authorEllis, Kathryn A-
dc.contributor.authorMartins, Ralph N-
dc.contributor.authorMaruff, Paul-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorRomano, Gary-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorSavage, Greg-
dc.contributor.authorMacaulay, S Lance-
dc.contributor.authorNarayan, Vaibhav A-
dc.date2015-
dc.date.accessioned2016-09-11T04:12:32Z-
dc.date.available2016-09-11T04:12:32Z-
dc.date.issued2015-
dc.identifier.citationJournal of Alzheimer's Disease 2015; 46(4): 1079-1089en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16218-
dc.description.abstractBackground: There is a growing consensus that disease-modifying therapies must be given at the prodromal or preclinical stages of Alzheimer’s disease (AD) to be effective. A major unmet need is to develop and validate sensitive measures to track disease progression in these populations. Objective: To generate novel statistically-derived composites from standard scores, which have increased sensitivity in the assessment of change from baseline in prodromal AD. Methods: An empirically based method was employed to generate domain specific, global, and cognitive-functional novel composites. The novel composites were compared and contrasted with each other, as well as standard scores for their ability to track change from baseline. The longitudinal characteristics and power to detect decline of the measures were evaluated. Data from participants in the Australian Imaging, Biomarkers and Lifestyle (AIBL) Study characterized as mild cognitively impaired with high neocortical amyloid-β burden were utilized for the study. Results: The best performing standard scores were CDR Sum-of-Boxes and MMSE. The statistically-derived novel composites performed better than the standard scores from which they were derived. The domain-specific composites generally did not perform as well as the global composites or the cognitive-functional composites. Conclusion: A systematic method was employed to generate novel statistically-derived composite measures from standard scores. Composites comprised of measures including function and multiple cognitive domains appeared to best capture change from baseline. These composites may be useful to assess progression or lack thereof in prodromal AD. However, the results should be replicated and validated using an independent clinical sample before implementation in a clinical trial.en_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectClinical markeren_US
dc.subjectMild cognitive impairmenten_US
dc.subjectNeuroimagingen_US
dc.subjectProdromal symptomsen_US
dc.titleNovel statistically-derived composite measures for assessing the efficacy of disease-modifying therapies in prodromal Alzheimer’s disease trials: an AIBL studyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Alzheimer's Diseaseen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationCSIRO Digital Productivity Flagship, Floreat, Western Australia, Australiaen_US
dc.identifier.affiliationJanssen Research and Development, Raritan, NJ, USAen_US
dc.identifier.affiliationCSIRO Digital Productivity Flagship, North Ryde, NSW, Australiaen_US
dc.identifier.affiliationJanssen Research and Development, Titusville, NJ, USAen_US
dc.identifier.affiliationJanssen Research and Development, Fremont, CA, USAen_US
dc.identifier.affiliationAcademic Unit for Psychiatry of Old Age, Department of Psychiatry, University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationNational Ageing Research Institute, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationCentre of Excellence for Alzheimer’s Disease Research & Care, School of Medical Sciences, Edith Cowan University, Joondalup, Western Australia, Australiaen_US
dc.identifier.affiliationSir James McCusker Alzheimer’s Disease Research Unit (Hollywood Private Hospital), Perth, Western Australia, Australiaen_US
dc.identifier.affiliationCogstate, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationMental Health Research Institute (MHRI), The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationARC Centre of Excellence in Cognition and its Disorders, and Department of Psychology, Macquarie University, Sydney, NSW, Australiaen_US
dc.identifier.affiliationCSIRO Food and Nutrition Flagship, Melbourne, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/26402634en_US
dc.identifier.doi10.3233/JAD-143015en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-3910-2453en_US
dc.type.austinJournal Articleen_US
local.name.researcherMasters, Colin L
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMolecular Imaging and Therapy-
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