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Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies
BACKGROUND & OBJECTIVE: Percent whole brain volume change (PBVC) measured from serial MRI scans is widely accepted as a sensitive marker of disease progression in Alzheimer's disease (AD). However, the utility of PBVC in the differential diagnosis of dementia remains to be established. We c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325088/ https://www.ncbi.nlm.nih.gov/pubmed/25685712 http://dx.doi.org/10.1016/j.nicl.2015.01.017 |
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author | Mak, Elijah Su, Li Williams, Guy B. Watson, Rosie Firbank, Michael Blamire, Andrew M. O'Brien, John T. |
author_facet | Mak, Elijah Su, Li Williams, Guy B. Watson, Rosie Firbank, Michael Blamire, Andrew M. O'Brien, John T. |
author_sort | Mak, Elijah |
collection | PubMed |
description | BACKGROUND & OBJECTIVE: Percent whole brain volume change (PBVC) measured from serial MRI scans is widely accepted as a sensitive marker of disease progression in Alzheimer's disease (AD). However, the utility of PBVC in the differential diagnosis of dementia remains to be established. We compared PBVC in AD and dementia with Lewy bodies (DLB), and investigated associations with clinical measures. METHODS: 72 participants (14 DLBs, 25 ADs, and 33 healthy controls (HCs)) underwent clinical assessment and 3 Tesla T1-weighted MRI at baseline and repeated at 12 months. We used FSL-SIENA to estimate PBVC for each subject. Voxelwise analyses and ANCOVA compared PBVC between DLB and AD, while correlational tests examined associations of PBVC with clinical measures. RESULTS: AD had significantly greater atrophy over 1 year (1.8%) compared to DLB (1.0%; p = 0.01) and HC (0.9%; p < 0.01) in widespread regions of the brain including periventricular areas. PBVC was not significantly different between DLB and HC (p = 0.95). There were no differences in cognitive decline between DLB and AD. In the combined dementia group (AD and DLB), younger age was associated with higher atrophy rates (r = 0.49, p < 0.01). CONCLUSIONS: AD showed a faster rate of global brain atrophy compared to DLB, which had similar rates of atrophy to HC. Among dementia subjects, younger age was associated with accelerated atrophy, reflecting more aggressive disease in younger people. PBVC could aid in differentiating between DLB and AD, however its utility as an outcome marker in DLB is limited. |
format | Online Article Text |
id | pubmed-4325088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-43250882015-02-14 Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies Mak, Elijah Su, Li Williams, Guy B. Watson, Rosie Firbank, Michael Blamire, Andrew M. O'Brien, John T. Neuroimage Clin Regular Article BACKGROUND & OBJECTIVE: Percent whole brain volume change (PBVC) measured from serial MRI scans is widely accepted as a sensitive marker of disease progression in Alzheimer's disease (AD). However, the utility of PBVC in the differential diagnosis of dementia remains to be established. We compared PBVC in AD and dementia with Lewy bodies (DLB), and investigated associations with clinical measures. METHODS: 72 participants (14 DLBs, 25 ADs, and 33 healthy controls (HCs)) underwent clinical assessment and 3 Tesla T1-weighted MRI at baseline and repeated at 12 months. We used FSL-SIENA to estimate PBVC for each subject. Voxelwise analyses and ANCOVA compared PBVC between DLB and AD, while correlational tests examined associations of PBVC with clinical measures. RESULTS: AD had significantly greater atrophy over 1 year (1.8%) compared to DLB (1.0%; p = 0.01) and HC (0.9%; p < 0.01) in widespread regions of the brain including periventricular areas. PBVC was not significantly different between DLB and HC (p = 0.95). There were no differences in cognitive decline between DLB and AD. In the combined dementia group (AD and DLB), younger age was associated with higher atrophy rates (r = 0.49, p < 0.01). CONCLUSIONS: AD showed a faster rate of global brain atrophy compared to DLB, which had similar rates of atrophy to HC. Among dementia subjects, younger age was associated with accelerated atrophy, reflecting more aggressive disease in younger people. PBVC could aid in differentiating between DLB and AD, however its utility as an outcome marker in DLB is limited. Elsevier 2015-02-07 /pmc/articles/PMC4325088/ /pubmed/25685712 http://dx.doi.org/10.1016/j.nicl.2015.01.017 Text en © 2015 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Mak, Elijah Su, Li Williams, Guy B. Watson, Rosie Firbank, Michael Blamire, Andrew M. O'Brien, John T. Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title | Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title_full | Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title_fullStr | Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title_full_unstemmed | Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title_short | Longitudinal assessment of global and regional atrophy rates in Alzheimer's disease and dementia with Lewy bodies |
title_sort | longitudinal assessment of global and regional atrophy rates in alzheimer's disease and dementia with lewy bodies |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325088/ https://www.ncbi.nlm.nih.gov/pubmed/25685712 http://dx.doi.org/10.1016/j.nicl.2015.01.017 |
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