Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28344
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dc.contributor.authorGardener, Samantha L-
dc.contributor.authorRainey-Smith, Stephanie R-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorFripp, Jurgen-
dc.contributor.authorDoré, Vincent-
dc.contributor.authorBourgeat, Pierrick-
dc.contributor.authorTaddei, Kevin-
dc.contributor.authorFowler, Christopher-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorMaruff, Paul-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorAmes, David-
dc.contributor.authorMartins, Ralph N-
dc.date2021-
dc.date.accessioned2021-12-14T03:12:58Z-
dc.date.available2021-12-14T03:12:58Z-
dc.date.issued2021-11-19-
dc.identifier.citationFrontiers in Aging Neuroscience 2021; 13: 744872.en
dc.identifier.issn1663-4365
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28344-
dc.description.abstractBackground: Worldwide, coffee is one of the most popular beverages consumed. Several studies have suggested a protective role of coffee, including reduced risk of Alzheimer's disease (AD). However, there is limited longitudinal data from cohorts of older adults reporting associations of coffee intake with cognitive decline, in distinct domains, and investigating the neuropathological mechanisms underpinning any such associations. Methods: The aim of the current study was to investigate the relationship between self-reported habitual coffee intake, and cognitive decline assessed using a comprehensive neuropsychological battery in 227 cognitively normal older adults from the Australian Imaging, Biomarkers, and Lifestyle (AIBL) study, over 126 months. In a subset of individuals, we also investigated the relationship between habitual coffee intake and cerebral Aβ-amyloid accumulation (n = 60) and brain volumes (n = 51) over 126 months. Results: Higher baseline coffee consumption was associated with slower cognitive decline in executive function, attention, and the AIBL Preclinical AD Cognitive Composite (PACC; shown reliably to measure the first signs of cognitive decline in at-risk cognitively normal populations), and lower likelihood of transitioning to mild cognitive impairment or AD status, over 126 months. Higher baseline coffee consumption was also associated with slower Aβ-amyloid accumulation over 126 months, and lower risk of progressing to "moderate," "high," or "very high" Aβ-amyloid burden status over the same time-period. There were no associations between coffee intake and atrophy in total gray matter, white matter, or hippocampal volume. Discussion: Our results further support the hypothesis that coffee intake may be a protective factor against AD, with increased coffee consumption potentially reducing cognitive decline by slowing cerebral Aβ-amyloid accumulation, and thus attenuating the associated neurotoxicity from Aβ-amyloid-mediated oxidative stress and inflammatory processes. Further investigation is required to evaluate whether coffee intake could be incorporated as a modifiable lifestyle factor aimed at delaying AD onset.en
dc.language.isoeng
dc.subjectAIBLen
dc.subjectAlzheimer’s diseaseen
dc.subjectAustralian Imaging Biomarkers and Lifestyle flagship study of ageingen
dc.subjectAβ-amyloiden
dc.subjectcaffeineen
dc.subjectcoffeeen
dc.subjectcognitive declineen
dc.subjectdementiaen
dc.titleHigher Coffee Consumption Is Associated With Slower Cognitive Decline and Less Cerebral Aβ-Amyloid Accumulation Over 126 Months: Data From the Australian Imaging, Biomarkers, and Lifestyle Study.en
dc.typeJournal Articleen
dc.identifier.journaltitleFrontiers in Aging Neuroscienceen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationCSIRO Health and Biosecurity/Australian e-Health Research Centre, Herston, QLD, Australiaen
dc.identifier.affiliationDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, United Statesen
dc.identifier.affiliationCentre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australiaen
dc.identifier.affiliationAustralian Alzheimer's Research Foundation, Sarich Neuroscience Research Institute, Perth, WA, Australiaen
dc.identifier.affiliationCentre for Healthy Ageing, Health Futures Institute, Murdoch University, Murdoch, WA, Australiaen
dc.identifier.affiliationSchool of Psychological Science, University of Western Australia, Perth, WA, Australiaen
dc.identifier.affiliationDepartment of Biomedical Sciences, Macquarie University, Sydney, NSW, Australiaen
dc.identifier.affiliationCogstate Ltd., Melbourne, VIC, Australiaen
dc.identifier.affiliationNational Ageing Research Institute, Parkville, VIC, Australiaen
dc.identifier.affiliationAcademic Unit for Psychiatry of Old Age, University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34867277/en
dc.identifier.doi10.3389/fnagi.2021.744872en
dc.type.contentTexten
dc.identifier.orcid0000-0002-8051-0558en
dc.identifier.orcid0000-0003-1397-0359en
dc.identifier.orcid0000-0003-3072-7940en
dc.identifier.orcid0000-0003-3910-2453en
dc.identifier.orcid0000-0002-6947-9537en
dc.identifier.pubmedid34867277
local.name.researcherDoré, Vincent
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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-
crisitem.author.deptMolecular Imaging and Therapy-
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