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dc.rights.licenseopenen_US
dc.contributor.authorMA, Yuan
dc.contributor.authorBLACKER, Deborah
dc.contributor.authorVISWANATHAN, Anand
dc.contributor.authorVAN VELUW, Susanne J.
dc.contributor.authorBOS, Daniel
dc.contributor.authorVERNOOIJ, Meike W.
dc.contributor.authorHYMAN, Bradley T.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorTZOURIO, Christophe
dc.contributor.authorDAS, Sudeshna
dc.contributor.authorHOFMAN, Albert
dc.date.accessioned2021-06-29T10:18:52Z
dc.date.available2021-06-29T10:18:52Z
dc.date.issued2021-04-26
dc.identifier.issn0028-3878en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/79326
dc.description.abstractEnOBJECTIVE: Large systolic blood pressure (SBP) variability has been proposed as a novel risk factor for dementia above and beyond SBP levels, but the underlying neuropathology is largely unknown. We investigated the relationship among visit-to-visit SBP variability, cognitive deterioration and underlying neuropathological changes. METHODS: We used longitudinal data (between 2005 and 2019) from the National Alzheimer's Coordinating Center. 13,284 dementia-free participants aged≥50 years were followed over a median of 5.0 (interquartile range: 3.1-7.6) years. Neuropathology data were available in 1,400 autopsied participants. Visit-to-visit SBP variability was quantified from repeated annual SBP measurements. Cognitive deterioration was defined as conversion from normal cognition to mild cognitive impairment (MCI) or dementia, or from MCI to dementia. RESULTS: Larger visit-to-visit SBP variability was associated with cognitive deterioration (adjusted odds ratio comparing extreme quintiles: 2.64; 95%CI:2.29-3.04, P <0.001). It was also associated with a higher burden of vascular pathology (including microinfarcts, white matter lesion, atherosclerosis of the circle of Willis and arteriolosclerosis) and with neurofibrillary tangle pathology assessed by Braak staging (All P < 0.05). The association with cognitive deterioration and vascular pathology appeared stronger among those with normal cognition versus MCI at baseline. These findings were observed after adjusting for age, sex, mean SBP and other confounding variables. Similar results were observed for diastolic BP variability. CONCLUSION: Larger visit-to-visit SBP variability was associated with cognitive deterioration. It was also associated with cerebrovascular pathology and neurofibrillary tangles. These results suggest the intertwined role of vascular and Alzheimer's disease pathology in the etiology of dementia.
dc.language.isoENen_US
dc.subject.enAll epidemiology
dc.subject.enAll Cognitive Disorders/Dementia
dc.subject.enAlzheimer's disease
dc.subject.enCohort studies
dc.title.enVisit-to-Visit Blood Pressure Variability, Neuropathology, and Cognitive Function
dc.typeArticle de revueen_US
dc.identifier.doi10.1212/wnl.0000000000012065en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33903194en_US
bordeaux.journalNeurologyen_US
bordeaux.volume96en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue23en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamHEALTHY_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03273581
hal.version1
hal.date.transferred2021-06-29T10:18:55Z
hal.exporttrue
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