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dc.contributor.authorPålhaugen, Lene
dc.contributor.authorSudre, Carole H
dc.contributor.authorTeceläo, Sandra Raquel Ramos
dc.contributor.authorNakling, Arne
dc.contributor.authorAlmdahl, Ina Selseth
dc.contributor.authorKalheim, Lisa Flem
dc.contributor.authorCardoso, M Jorge
dc.contributor.authorJohnsen, Stein Harald
dc.contributor.authorRongve, Arvid
dc.contributor.authorAarsland, Dag
dc.contributor.authorBjørnerud, Atle
dc.contributor.authorSelnes, Per
dc.contributor.authorFladby, Tormod
dc.date.accessioned2020-11-20T13:08:41Z
dc.date.available2020-11-20T13:08:41Z
dc.date.issued2020-09-21
dc.description.abstractWhite matter hyperintensities (WMHs) are associated with vascular risk and Alzheimer’s disease. In this study, we examined relations between WMH load and distribution, amyloid pathology and vascular risk in 339 controls and cases with either subjective (SCD) or mild cognitive impairment (MCI). Regional deep (DWMH) and periventricular (PWMH) WMH loads were determined using an automated algorithm. We stratified on Aβ1-42 pathology (Aβ+/−) and analyzed group differences, as well as associations with Framingham Risk Score for cardiovascular disease (FRS-CVD) and age. Occipital PWMH (<i>p</i> = 0.001) and occipital DWMH (<i>p</i> = 0.003) loads were increased in SCD-Aβ+ compared with Aβ− controls. In MCI-Aβ+ compared with Aβ− controls, there were differences in global WMH (<i>p</i> = 0.003), as well as occipital DWMH (<i>p</i> = 0.001) and temporal DWMH (<i>p</i> = 0.002) loads. FRS-CVD was associated with frontal PWMHs (<i>p</i> = 0.003) and frontal DWMHs (<i>p</i> = 0.005), after adjusting for age. There were associations between global and all regional WMH loads and age. In summary, posterior WMH loads were increased in SCD-Aβ+ and MCI-Aβ+ cases, whereas frontal WMHs were associated with vascular risk. The differences in WMH topography support the use of regional WMH load as an early-stage marker of etiology.en_US
dc.identifier.citationPålhaugen, Sudre, Teceläo, Nakling, Almdahl, Kalheim, Cardoso, Johnsen, Rongve, Aarsland, Bjørnerud, Selnes, Fladby. Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns. Journal of Cerebral Blood Flow and Metabolism. 2020:1-13en_US
dc.identifier.cristinIDFRIDAID 1833921
dc.identifier.doi10.1177/0271678X20957604
dc.identifier.issn0271-678X
dc.identifier.issn1559-7016
dc.identifier.urihttps://hdl.handle.net/10037/19891
dc.language.isoengen_US
dc.publisherSAGE Publicationsen_US
dc.relation.journalJournal of Cerebral Blood Flow and Metabolism
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/BEHANDLING/269774/Norway/269774/The Norwegian Node of the International Neuroinformatic Coordinating Facility/en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2020 The Author(s)en_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710en_US
dc.titleBrain amyloid and vascular risk are related to distinct white matter hyperintensity patternsen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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