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Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns

White 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). Regio...

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Autores principales: Pålhaugen, Lene, Sudre, Carole H, Tecelao, Sandra, Nakling, Arne, Almdahl, Ina S, Kalheim, Lisa F, Cardoso, M Jorge, Johnsen, Stein H, Rongve, Arvid, Aarsland, Dag, Bjørnerud, Atle, Selnes, Per, Fladby, Tormod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054718/
https://www.ncbi.nlm.nih.gov/pubmed/32955960
http://dx.doi.org/10.1177/0271678X20957604
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author Pålhaugen, Lene
Sudre, Carole H
Tecelao, Sandra
Nakling, Arne
Almdahl, Ina S
Kalheim, Lisa F
Cardoso, M Jorge
Johnsen, Stein H
Rongve, Arvid
Aarsland, Dag
Bjørnerud, Atle
Selnes, Per
Fladby, Tormod
author_facet Pålhaugen, Lene
Sudre, Carole H
Tecelao, Sandra
Nakling, Arne
Almdahl, Ina S
Kalheim, Lisa F
Cardoso, M Jorge
Johnsen, Stein H
Rongve, Arvid
Aarsland, Dag
Bjørnerud, Atle
Selnes, Per
Fladby, Tormod
author_sort Pålhaugen, Lene
collection PubMed
description White 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.
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spelling pubmed-80547182021-05-03 Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns Pålhaugen, Lene Sudre, Carole H Tecelao, Sandra Nakling, Arne Almdahl, Ina S Kalheim, Lisa F Cardoso, M Jorge Johnsen, Stein H Rongve, Arvid Aarsland, Dag Bjørnerud, Atle Selnes, Per Fladby, Tormod J Cereb Blood Flow Metab Original Articles White 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. SAGE Publications 2020-09-21 2021-05 /pmc/articles/PMC8054718/ /pubmed/32955960 http://dx.doi.org/10.1177/0271678X20957604 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Pålhaugen, Lene
Sudre, Carole H
Tecelao, Sandra
Nakling, Arne
Almdahl, Ina S
Kalheim, Lisa F
Cardoso, M Jorge
Johnsen, Stein H
Rongve, Arvid
Aarsland, Dag
Bjørnerud, Atle
Selnes, Per
Fladby, Tormod
Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title_full Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title_fullStr Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title_full_unstemmed Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title_short Brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
title_sort brain amyloid and vascular risk are related to distinct white matter hyperintensity patterns
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054718/
https://www.ncbi.nlm.nih.gov/pubmed/32955960
http://dx.doi.org/10.1177/0271678X20957604
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