Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16697
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dc.contributor.authorPatel, Sheila K-
dc.contributor.authorRestrepo, Carolina-
dc.contributor.authorWerden, Emilio-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorEkinci, Elif I-
dc.contributor.authorSrivastava, Piyush M-
dc.contributor.authorRamchand, Jay-
dc.contributor.authorWai, Bryan-
dc.contributor.authorChambers, Brian R-
dc.contributor.authorO’Callaghan, Christopher J-
dc.contributor.authorDarby, David-
dc.contributor.authorHachinski, Vladimir-
dc.contributor.authorCumming, Toby B-
dc.contributor.authorDonnan, Geoffrey A-
dc.contributor.authorBurrell, Louise M-
dc.contributor.authorBrodtmann, Amy-
dc.date.accessioned2017-06-29T02:46:59Z-
dc.date.available2017-06-29T02:46:59Z-
dc.date.issued2017-04-07-
dc.identifier.citationBMC Endocrine Disorders 2017; 17(1): 24en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16697-
dc.description.abstractBACKGROUND: Cognitive impairment is common in type 2 diabetes mellitus, and there is a strong association between type 2 diabetes and Alzheimer's disease. However, we do not know which type 2 diabetes patients will dement or which biomarkers predict cognitive decline. Left ventricular hypertrophy (LVH) is potentially such a marker. LVH is highly prevalent in type 2 diabetes and is a strong, independent predictor of cardiovascular events. To date, no studies have investigated the association between LVH and cognitive decline in type 2 diabetes. The Diabetes and Dementia (D2) study is designed to establish whether patients with type 2 diabetes and LVH have increased rates of brain atrophy and cognitive decline. METHODS: The D2 study is a single centre, observational, longitudinal case control study that will follow 168 adult patients aged >50 years with type 2 diabetes: 50% with LVH (case) and 50% without LVH (control). It will assess change in cardiovascular risk, brain imaging and neuropsychological testing between two time-points, baseline (0 months) and 24 months. The primary outcome is brain volume change at 24 months. The co-primary outcome is the presence of cognitive decline at 24 months. The secondary outcome is change in left ventricular mass associated with brain atrophy and cognitive decline at 24 months. DISCUSSION: The D2 study will test the hypothesis that patients with type 2 diabetes and LVH will exhibit greater brain atrophy than those without LVH. An understanding of whether LVH contributes to cognitive decline, and in which patients, will allow us to identify patients at particular risk. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ( ACTRN12616000546459 ), date registered, 28/04/2016.en_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectCognitionen_US
dc.subjectD2 studyen_US
dc.subjectDementiaen_US
dc.subjectLeft ventricular hypertrophyen_US
dc.subjectType 2 diabetes mellitusen_US
dc.titleDoes left ventricular hypertrophy affect cognition and brain structural integrity in type 2 diabetes? Study design and rationale of the Diabetes and Dementia (D2) studyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMC Endocrine Disordersen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationNeurologyen_US
dc.identifier.affiliationClinical Pharmacology and Therapeuticsen_US
dc.identifier.affiliationDepartment of Clinical Neurological Sciences, London Health Sciences Centre, University of Western Ontario, London, Canadaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28388897en_US
dc.identifier.doi10.1186/s12902-017-0173-7en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-1863-7539en_US
dc.type.austinJournal Articleen_US
local.name.researcherBrodtmann, Amy
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCardiology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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