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Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study

Atrophy is regarded a sensitive marker of neurodegenerative pathology. In addition to confirming the well-known presence of decreased global grey matter and hippocampal volumes in Alzheimer's disease, this study investigated whether deep grey matter structure also suffer degeneration in Alzheim...

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Autores principales: de Jong, L. W., van der Hiele, K., Veer, I. M., Houwing, J. J., Westendorp, R. G. J., Bollen, E. L. E. M., de Bruin, P. W., Middelkoop, H. A. M., van Buchem, M. A., van der Grond, J.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639208/
https://www.ncbi.nlm.nih.gov/pubmed/19022861
http://dx.doi.org/10.1093/brain/awn278
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author de Jong, L. W.
van der Hiele, K.
Veer, I. M.
Houwing, J. J.
Westendorp, R. G. J.
Bollen, E. L. E. M.
de Bruin, P. W.
Middelkoop, H. A. M.
van Buchem, M. A.
van der Grond, J.
author_facet de Jong, L. W.
van der Hiele, K.
Veer, I. M.
Houwing, J. J.
Westendorp, R. G. J.
Bollen, E. L. E. M.
de Bruin, P. W.
Middelkoop, H. A. M.
van Buchem, M. A.
van der Grond, J.
author_sort de Jong, L. W.
collection PubMed
description Atrophy is regarded a sensitive marker of neurodegenerative pathology. In addition to confirming the well-known presence of decreased global grey matter and hippocampal volumes in Alzheimer's disease, this study investigated whether deep grey matter structure also suffer degeneration in Alzheimer's disease, and whether such degeneration is associated with cognitive deterioration. In this cross-sectional correlation study, two groups were compared on volumes of seven subcortical regions: 70 memory complainers (MCs) and 69 subjects diagnosed with probable Alzheimer's disease. Using 3T 3D T1 MR images, volumes of nucleus accumbens, amygdala, caudate nucleus, hippocampus, pallidum, putamen and thalamus were automatically calculated by the FMRIB's Integrated Registration and Segmentation Tool (FIRST)—algorithm FMRIB's Software Library (FSL). Subsequently, the volumes of the different regions were correlated with cognitive test results. In addition to finding the expected association between hippocampal atrophy and cognitive decline in Alzheimer's disease, volumes of putamen and thalamus were significantly reduced in patients diagnosed with probable Alzheimer's disease. We also found that the decrease in volume correlated linearly with impaired global cognitive performance. These findings strongly suggest that, beside neo-cortical atrophy, deep grey matter structures in Alzheimer's disease suffer atrophy as well and that degenerative processes in the putamen and thalamus, like the hippocampus, may contribute to cognitive decline in Alzheimer's disease.
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spelling pubmed-26392082009-02-25 Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study de Jong, L. W. van der Hiele, K. Veer, I. M. Houwing, J. J. Westendorp, R. G. J. Bollen, E. L. E. M. de Bruin, P. W. Middelkoop, H. A. M. van Buchem, M. A. van der Grond, J. Brain Original Articles Atrophy is regarded a sensitive marker of neurodegenerative pathology. In addition to confirming the well-known presence of decreased global grey matter and hippocampal volumes in Alzheimer's disease, this study investigated whether deep grey matter structure also suffer degeneration in Alzheimer's disease, and whether such degeneration is associated with cognitive deterioration. In this cross-sectional correlation study, two groups were compared on volumes of seven subcortical regions: 70 memory complainers (MCs) and 69 subjects diagnosed with probable Alzheimer's disease. Using 3T 3D T1 MR images, volumes of nucleus accumbens, amygdala, caudate nucleus, hippocampus, pallidum, putamen and thalamus were automatically calculated by the FMRIB's Integrated Registration and Segmentation Tool (FIRST)—algorithm FMRIB's Software Library (FSL). Subsequently, the volumes of the different regions were correlated with cognitive test results. In addition to finding the expected association between hippocampal atrophy and cognitive decline in Alzheimer's disease, volumes of putamen and thalamus were significantly reduced in patients diagnosed with probable Alzheimer's disease. We also found that the decrease in volume correlated linearly with impaired global cognitive performance. These findings strongly suggest that, beside neo-cortical atrophy, deep grey matter structures in Alzheimer's disease suffer atrophy as well and that degenerative processes in the putamen and thalamus, like the hippocampus, may contribute to cognitive decline in Alzheimer's disease. Oxford University Press 2008-12 2008-11-20 /pmc/articles/PMC2639208/ /pubmed/19022861 http://dx.doi.org/10.1093/brain/awn278 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
de Jong, L. W.
van der Hiele, K.
Veer, I. M.
Houwing, J. J.
Westendorp, R. G. J.
Bollen, E. L. E. M.
de Bruin, P. W.
Middelkoop, H. A. M.
van Buchem, M. A.
van der Grond, J.
Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title_full Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title_fullStr Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title_full_unstemmed Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title_short Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study
title_sort strongly reduced volumes of putamen and thalamus in alzheimer's disease: an mri study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639208/
https://www.ncbi.nlm.nih.gov/pubmed/19022861
http://dx.doi.org/10.1093/brain/awn278
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