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White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy

This study investigates relationships between white matter hyperintensity (WMH) volume, cerebrospinal fluid (CSF) Alzheimer's disease (AD) pathology markers, and brain and hippocampal volume loss. Subjects included 198 controls, 345 mild cognitive impairment (MCI), and 154 AD subjects with seri...

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Autores principales: Fiford, Cassidy M., Manning, Emily N., Bartlett, Jonathan W., Cash, David M., Malone, Ian B., Ridgway, Gerard R., Lehmann, Manja, Leung, Kelvin K., Sudre, Carole H., Ourselin, Sebastien, Biessels, Geert Jan, Carmichael, Owen T., Fox, Nick C., Cardoso, M. Jorge, Barnes, Josephine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324634/
https://www.ncbi.nlm.nih.gov/pubmed/27933676
http://dx.doi.org/10.1002/hipo.22690
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author Fiford, Cassidy M.
Manning, Emily N.
Bartlett, Jonathan W.
Cash, David M.
Malone, Ian B.
Ridgway, Gerard R.
Lehmann, Manja
Leung, Kelvin K.
Sudre, Carole H.
Ourselin, Sebastien
Biessels, Geert Jan
Carmichael, Owen T.
Fox, Nick C.
Cardoso, M. Jorge
Barnes, Josephine
author_facet Fiford, Cassidy M.
Manning, Emily N.
Bartlett, Jonathan W.
Cash, David M.
Malone, Ian B.
Ridgway, Gerard R.
Lehmann, Manja
Leung, Kelvin K.
Sudre, Carole H.
Ourselin, Sebastien
Biessels, Geert Jan
Carmichael, Owen T.
Fox, Nick C.
Cardoso, M. Jorge
Barnes, Josephine
author_sort Fiford, Cassidy M.
collection PubMed
description This study investigates relationships between white matter hyperintensity (WMH) volume, cerebrospinal fluid (CSF) Alzheimer's disease (AD) pathology markers, and brain and hippocampal volume loss. Subjects included 198 controls, 345 mild cognitive impairment (MCI), and 154 AD subjects with serial volumetric 1.5‐T MRI. CSF Aβ(42) and total tau were measured (n = 353). Brain and hippocampal loss were quantified from serial MRI using the boundary shift integral (BSI). Multiple linear regression models assessed the relationships between WMHs and hippocampal and brain atrophy rates. Models were refitted adjusting for (a) concurrent brain/hippocampal atrophy rates and (b) CSF Aβ(42) and tau in subjects with CSF data. WMH burden was positively associated with hippocampal atrophy rate in controls (P = 0.002) and MCI subjects (P = 0.03), and with brain atrophy rate in controls (P = 0.03). The associations with hippocampal atrophy rate remained following adjustment for concurrent brain atrophy rate in controls and MCIs, and for CSF biomarkers in controls (P = 0.007). These novel results suggest that vascular damage alongside AD pathology is associated with disproportionately greater hippocampal atrophy in nondemented older adults. © 2016 The Authors Hippocampus Published by Wiley Periodicals, Inc.
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spelling pubmed-53246342017-03-08 White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy Fiford, Cassidy M. Manning, Emily N. Bartlett, Jonathan W. Cash, David M. Malone, Ian B. Ridgway, Gerard R. Lehmann, Manja Leung, Kelvin K. Sudre, Carole H. Ourselin, Sebastien Biessels, Geert Jan Carmichael, Owen T. Fox, Nick C. Cardoso, M. Jorge Barnes, Josephine Hippocampus Research Articles This study investigates relationships between white matter hyperintensity (WMH) volume, cerebrospinal fluid (CSF) Alzheimer's disease (AD) pathology markers, and brain and hippocampal volume loss. Subjects included 198 controls, 345 mild cognitive impairment (MCI), and 154 AD subjects with serial volumetric 1.5‐T MRI. CSF Aβ(42) and total tau were measured (n = 353). Brain and hippocampal loss were quantified from serial MRI using the boundary shift integral (BSI). Multiple linear regression models assessed the relationships between WMHs and hippocampal and brain atrophy rates. Models were refitted adjusting for (a) concurrent brain/hippocampal atrophy rates and (b) CSF Aβ(42) and tau in subjects with CSF data. WMH burden was positively associated with hippocampal atrophy rate in controls (P = 0.002) and MCI subjects (P = 0.03), and with brain atrophy rate in controls (P = 0.03). The associations with hippocampal atrophy rate remained following adjustment for concurrent brain atrophy rate in controls and MCIs, and for CSF biomarkers in controls (P = 0.007). These novel results suggest that vascular damage alongside AD pathology is associated with disproportionately greater hippocampal atrophy in nondemented older adults. © 2016 The Authors Hippocampus Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2017-01-09 2017-03 /pmc/articles/PMC5324634/ /pubmed/27933676 http://dx.doi.org/10.1002/hipo.22690 Text en © 2016 The Authors Hippocampus Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Fiford, Cassidy M.
Manning, Emily N.
Bartlett, Jonathan W.
Cash, David M.
Malone, Ian B.
Ridgway, Gerard R.
Lehmann, Manja
Leung, Kelvin K.
Sudre, Carole H.
Ourselin, Sebastien
Biessels, Geert Jan
Carmichael, Owen T.
Fox, Nick C.
Cardoso, M. Jorge
Barnes, Josephine
White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title_full White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title_fullStr White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title_full_unstemmed White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title_short White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
title_sort white matter hyperintensities are associated with disproportionate progressive hippocampal atrophy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324634/
https://www.ncbi.nlm.nih.gov/pubmed/27933676
http://dx.doi.org/10.1002/hipo.22690
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