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dc.date.accessioned2020-11-30T20:30:57Z
dc.date.available2020-11-30T20:30:57Z
dc.date.created2020-09-28T09:07:17Z
dc.date.issued2020
dc.identifier.citationPålhaugen, Lene Sudre, Carole H Teceläo, Sandra Raquel Ramos Nakling, Arne Almdahl, Ina Selseth Kalheim, Lisa Flem Cardoso, M Jorge Johnsen, Stein Harald Rongve, Arvid Aarsland, Dag Bjørnerud, Atle Selnes, Per Fladby, Tormod . Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns. Journal of Cerebral Blood Flow and Metabolism. 2020, 1-13
dc.identifier.urihttp://hdl.handle.net/10852/81302
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 ( p = 0.001) and occipital DWMH ( p = 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 ( p = 0.003), as well as occipital DWMH ( p = 0.001) and temporal DWMH ( p = 0.002) loads. FRS-CVD was associated with frontal PWMHs ( p = 0.003) and frontal DWMHs ( p = 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.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleBrain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
dc.typeJournal article
dc.creator.authorPålhaugen, Lene
dc.creator.authorSudre, Carole H
dc.creator.authorTeceläo, Sandra Raquel Ramos
dc.creator.authorNakling, Arne
dc.creator.authorAlmdahl, Ina Selseth
dc.creator.authorKalheim, Lisa Flem
dc.creator.authorCardoso, M Jorge
dc.creator.authorJohnsen, Stein Harald
dc.creator.authorRongve, Arvid
dc.creator.authorAarsland, Dag
dc.creator.authorBjørnerud, Atle
dc.creator.authorSelnes, Per
dc.creator.authorFladby, Tormod
cristin.unitcode185,53,82,0
cristin.unitnameKlinikk for indremedisin og laboratoriefag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1833921
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Cerebral Blood Flow and Metabolism&rft.volume=&rft.spage=1&rft.date=2020
dc.identifier.jtitleJournal of Cerebral Blood Flow and Metabolism
dc.identifier.doihttps://doi.org/10.1177/0271678X20957604
dc.identifier.urnURN:NBN:no-84371
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0271-678X
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/81302/2/0271678x20957604.pdf
dc.type.versionPublishedVersion
cristin.articleid0271678X2095760
dc.relation.projectNFR/269774


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