Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20955
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dc.contributor.authorStough, Con-
dc.contributor.authorNankivell, Madeleine-
dc.contributor.authorCamfield, David A-
dc.contributor.authorPerry, Naomi L-
dc.contributor.authorPipingas, Andrew-
dc.contributor.authorMacpherson, Helen-
dc.contributor.authorWesnes, Keith-
dc.contributor.authorOu, Ruchong-
dc.contributor.authorHare, David L-
dc.contributor.authorde Haan, Judy-
dc.contributor.authorHead, Geoffrey-
dc.contributor.authorLansjoen, Peter-
dc.contributor.authorLangsjoen, Alena-
dc.contributor.authorTan, Brendan-
dc.contributor.authorPase, Matthew P-
dc.contributor.authorKing, Rebecca-
dc.contributor.authorRowsell, Renee-
dc.contributor.authorZwalf, Oliver-
dc.contributor.authorRathner, Yossi-
dc.contributor.authorCooke, Matthew-
dc.contributor.authorRosenfeldt, Franklin-
dc.date2019-05-29-
dc.date.accessioned2019-06-19T06:28:51Z-
dc.date.available2019-06-19T06:28:51Z-
dc.date.issued2019-05-29-
dc.identifier.citationFrontiers in Aging Neuroscience 2019; 11: 103en_US
dc.identifier.issn1663-4365-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20955-
dc.description.abstractIntroduction: With an aging population there is an important need for the development of effective treatments for the amelioration of cognitive decline. Multiple mechanisms underlie age-related cognitive decline including cerebrovascular disease, oxidative stress, reduced antioxidant capacity and mitochondrial dysfunction. CoQ10 is a novel treatment which has the potential to improve brain function in healthy elderly populations due to established beneficial effects on mitochondrial function, vascular function and oxidative stress. Methods and Analysis: We describe the protocol for a 90-day randomized controlled trial which examines the efficacy of Ubiquinol (200 mg/day) vs. placebo for the amelioration of cognitive decline in a healthy (non-demented) elderly sample, aged 60 years and over. The primary outcome is the effect of Ubiquinol at 90 days compared to baseline on CogTrack composite measures of cognition. Additional cognitive measures, as well as measures of cardiovascular function, oxidative stress, liver function and mood will also be monitored across 30-, 60- and 90- day time points. Data analyses will involve repeated measures analysis of variance (ANOVA). Discussion: This study will be the first of its kind to provide important clinical and mechanistic data regarding the efficacy of Ubiquinol as a treatment for age-related cognitive decline in the healthy elderly with important implications for productivity and quality of life within this age group. Clinical Trial Registration: The trial has been registered with the Australian and New Zealand Clinical Trials Registry (ANZCTRN12618001841268).en_US
dc.language.isoeng-
dc.subjectCoenzyme Q10en_US
dc.subjectRCTen_US
dc.subjectUbiquinolen_US
dc.subjectagingen_US
dc.subjectcardiovascular functionen_US
dc.subjectcognitionen_US
dc.subjectcognitive declineen_US
dc.subjectdementiaen_US
dc.titleCoQ10 and Cognition a Review and Study Protocol for a 90-Day Randomized Controlled Trial Investigating the Cognitive Effects of Ubiquinol in the Healthy Elderly.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleFrontiers in Aging Neuroscienceen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationFaculty of Medicine, Dentistry, and Health Sciences, The University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationBaker Heart and Diabetes Institute, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Health and Medical Sciences, Swinburne University of Technology, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationFaculty of Health, Institute for Physical Activity and Nutrition, Deakin University, Geelong, Victoria, Australiaen_US
dc.identifier.affiliationCentre for Human Psychopharmacology, Swinburne University of Technology, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationWesnes Cognition Limited, Streatley on Thames, United Kingdomen_US
dc.identifier.affiliationDepartment of Psychology, Northumbria University, Newcastle, United Kingdomen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen_US
dc.identifier.affiliationEast Texas Medical Center and Trinity Mother Francis Hospital, Tyler, TX, United Statesen_US
dc.identifier.doi10.3389/fnagi.2019.00103en_US
dc.type.contentTexten_US
dc.identifier.pubmedid31191293-
dc.type.austinJournal Article-
local.name.researcherHare, David L
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptCardiology-
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