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Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease
BACKGROUND: This study examined the relationship between baseline white matter lesions (WMLs) and the progression of cognitive decline in patients with late-onset Alzheimer's disease (AD). METHODS: Fifty-six patients with AD were included in the study (23 men, 33 women; mean age, 77.8 years). A...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638977/ https://www.ncbi.nlm.nih.gov/pubmed/23637702 http://dx.doi.org/10.1159/000350317 |
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author | Kimura, Noriyuki Nakama, Hiroshi Nakamura, Kenichiro Aso, Yasuhiro Kumamoto, Toshihide |
author_facet | Kimura, Noriyuki Nakama, Hiroshi Nakamura, Kenichiro Aso, Yasuhiro Kumamoto, Toshihide |
author_sort | Kimura, Noriyuki |
collection | PubMed |
description | BACKGROUND: This study examined the relationship between baseline white matter lesions (WMLs) and the progression of cognitive decline in patients with late-onset Alzheimer's disease (AD). METHODS: Fifty-six patients with AD were included in the study (23 men, 33 women; mean age, 77.8 years). All subjects were treated with acetylcholinesterase inhibitors and followed up for approximately 1 year. The Mini-Mental State Examination (MMSE) score was assessed at least twice to evaluate the progressive cognitive impairment. All subjects underwent brain MRI at baseline and were divided into WMLs(-), mild WMLs(+), and moderate WMLs(+) groups based on WML severity. Changes in MMSE scores between baseline and follow-up were analyzed using the Wilcoxon signed-rank test. RESULTS: MMSE scores at baseline did not differ significantly among the three groups (p = 0.1658), whereas MMSE scores at the follow-up evaluation were significantly lower in the moderate WMLs(+) group than in the WMLs(-) group (p = 0.0257). The mean MMSE scores remained above baseline values during the approximately 1-year follow-up in the WMLs(-) group, whereas they were decreased in the mild and moderate WMLs(+) groups. Moreover, the frequency of improvement in patients from the WMLs(-) group tended to be higher than that in patients from the WMLs(+) groups. CONCLUSION: Baseline WMLs may be associated with the heterogeneous progression of cognitive decline in patients with AD. |
format | Online Article Text |
id | pubmed-3638977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-36389772013-05-01 Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease Kimura, Noriyuki Nakama, Hiroshi Nakamura, Kenichiro Aso, Yasuhiro Kumamoto, Toshihide Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND: This study examined the relationship between baseline white matter lesions (WMLs) and the progression of cognitive decline in patients with late-onset Alzheimer's disease (AD). METHODS: Fifty-six patients with AD were included in the study (23 men, 33 women; mean age, 77.8 years). All subjects were treated with acetylcholinesterase inhibitors and followed up for approximately 1 year. The Mini-Mental State Examination (MMSE) score was assessed at least twice to evaluate the progressive cognitive impairment. All subjects underwent brain MRI at baseline and were divided into WMLs(-), mild WMLs(+), and moderate WMLs(+) groups based on WML severity. Changes in MMSE scores between baseline and follow-up were analyzed using the Wilcoxon signed-rank test. RESULTS: MMSE scores at baseline did not differ significantly among the three groups (p = 0.1658), whereas MMSE scores at the follow-up evaluation were significantly lower in the moderate WMLs(+) group than in the WMLs(-) group (p = 0.0257). The mean MMSE scores remained above baseline values during the approximately 1-year follow-up in the WMLs(-) group, whereas they were decreased in the mild and moderate WMLs(+) groups. Moreover, the frequency of improvement in patients from the WMLs(-) group tended to be higher than that in patients from the WMLs(+) groups. CONCLUSION: Baseline WMLs may be associated with the heterogeneous progression of cognitive decline in patients with AD. S. Karger AG 2013-03-29 /pmc/articles/PMC3638977/ /pubmed/23637702 http://dx.doi.org/10.1159/000350317 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No-Derivative-Works License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Original Research Article Kimura, Noriyuki Nakama, Hiroshi Nakamura, Kenichiro Aso, Yasuhiro Kumamoto, Toshihide Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title | Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title_full | Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title_fullStr | Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title_full_unstemmed | Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title_short | Relationship between White Matter Lesions and Progression of Cognitive Decline in Alzheimer's Disease |
title_sort | relationship between white matter lesions and progression of cognitive decline in alzheimer's disease |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638977/ https://www.ncbi.nlm.nih.gov/pubmed/23637702 http://dx.doi.org/10.1159/000350317 |
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