Cargando…
White matter hyperintensity topography in Alzheimer's disease and links to cognition
INTRODUCTION: White matter hyperintensities (WMH) are often described in Alzheimer's disease (AD), but their topography and specific relationships with cognition remain unclear. METHODS: Regional WMH were estimated in 54 cognitively impaired amyloid beta–positive AD (Aβpos‐AD), compared to 40 c...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292254/ https://www.ncbi.nlm.nih.gov/pubmed/34322985 http://dx.doi.org/10.1002/alz.12410 |
_version_ | 1784749326226948096 |
---|---|
author | Garnier‐Crussard, Antoine Bougacha, Salma Wirth, Miranka Dautricourt, Sophie Sherif, Siya Landeau, Brigitte Gonneaud, Julie De Flores, Robin de la Sayette, Vincent Vivien, Denis Krolak‐Salmon, Pierre Chételat, Gaël |
author_facet | Garnier‐Crussard, Antoine Bougacha, Salma Wirth, Miranka Dautricourt, Sophie Sherif, Siya Landeau, Brigitte Gonneaud, Julie De Flores, Robin de la Sayette, Vincent Vivien, Denis Krolak‐Salmon, Pierre Chételat, Gaël |
author_sort | Garnier‐Crussard, Antoine |
collection | PubMed |
description | INTRODUCTION: White matter hyperintensities (WMH) are often described in Alzheimer's disease (AD), but their topography and specific relationships with cognition remain unclear. METHODS: Regional WMH were estimated in 54 cognitively impaired amyloid beta–positive AD (Aβpos‐AD), compared to 40 cognitively unimpaired amyloid beta–negative older controls (Aβneg‐controls) matched for vascular risk factors. The cross‐sectional association between regional WMH volume and cognition was assessed within each group, controlling for cerebral amyloid burden, global cortical atrophy, and hippocampal atrophy. RESULTS: WMH volume was larger in Aβpos‐AD compared to Aβneg‐controls in all regions, with the greatest changes in the splenium of the corpus callosum (S‐CC). In Aβpos‐AD patients, larger total and regional WMH volume, especially in the S‐CC, was strongly associated with decreased cognition. DISCUSSION: WMH specifically contribute to lower cognition in AD, independently from amyloid deposition and atrophy. This study emphasizes the clinical relevance of WMH in AD, especially posterior WMH, and most notably S‐CC WMH. |
format | Online Article Text |
id | pubmed-9292254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92922542022-07-20 White matter hyperintensity topography in Alzheimer's disease and links to cognition Garnier‐Crussard, Antoine Bougacha, Salma Wirth, Miranka Dautricourt, Sophie Sherif, Siya Landeau, Brigitte Gonneaud, Julie De Flores, Robin de la Sayette, Vincent Vivien, Denis Krolak‐Salmon, Pierre Chételat, Gaël Alzheimers Dement Featured Articles INTRODUCTION: White matter hyperintensities (WMH) are often described in Alzheimer's disease (AD), but their topography and specific relationships with cognition remain unclear. METHODS: Regional WMH were estimated in 54 cognitively impaired amyloid beta–positive AD (Aβpos‐AD), compared to 40 cognitively unimpaired amyloid beta–negative older controls (Aβneg‐controls) matched for vascular risk factors. The cross‐sectional association between regional WMH volume and cognition was assessed within each group, controlling for cerebral amyloid burden, global cortical atrophy, and hippocampal atrophy. RESULTS: WMH volume was larger in Aβpos‐AD compared to Aβneg‐controls in all regions, with the greatest changes in the splenium of the corpus callosum (S‐CC). In Aβpos‐AD patients, larger total and regional WMH volume, especially in the S‐CC, was strongly associated with decreased cognition. DISCUSSION: WMH specifically contribute to lower cognition in AD, independently from amyloid deposition and atrophy. This study emphasizes the clinical relevance of WMH in AD, especially posterior WMH, and most notably S‐CC WMH. John Wiley and Sons Inc. 2021-07-28 2022-03 /pmc/articles/PMC9292254/ /pubmed/34322985 http://dx.doi.org/10.1002/alz.12410 Text en © 2021 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Featured Articles Garnier‐Crussard, Antoine Bougacha, Salma Wirth, Miranka Dautricourt, Sophie Sherif, Siya Landeau, Brigitte Gonneaud, Julie De Flores, Robin de la Sayette, Vincent Vivien, Denis Krolak‐Salmon, Pierre Chételat, Gaël White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title | White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title_full | White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title_fullStr | White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title_full_unstemmed | White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title_short | White matter hyperintensity topography in Alzheimer's disease and links to cognition |
title_sort | white matter hyperintensity topography in alzheimer's disease and links to cognition |
topic | Featured Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292254/ https://www.ncbi.nlm.nih.gov/pubmed/34322985 http://dx.doi.org/10.1002/alz.12410 |
work_keys_str_mv | AT garniercrussardantoine whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT bougachasalma whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT wirthmiranka whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT dautricourtsophie whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT sherifsiya whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT landeaubrigitte whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT gonneaudjulie whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT defloresrobin whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT delasayettevincent whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT viviendenis whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT krolaksalmonpierre whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition AT chetelatgael whitematterhyperintensitytopographyinalzheimersdiseaseandlinkstocognition |