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Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia?
Background: Cerebral white matter lesions (WML), evident on CT and MRI brain scans, are histopathologically heterogeneous but associated with vascular risk factors and thought mainly to indicate ischemic damage. There has been disagreement over their clinical prognostic value in predicting conversio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518278/ https://www.ncbi.nlm.nih.gov/pubmed/22874528 http://dx.doi.org/10.1017/S1041610212000932 |
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author | Devine, Michael E. Fonseca, J. Andres Saez Walker, Zuzana |
author_facet | Devine, Michael E. Fonseca, J. Andres Saez Walker, Zuzana |
author_sort | Devine, Michael E. |
collection | PubMed |
description | Background: Cerebral white matter lesions (WML), evident on CT and MRI brain scans, are histopathologically heterogeneous but associated with vascular risk factors and thought mainly to indicate ischemic damage. There has been disagreement over their clinical prognostic value in predicting conversion from mild cognitive impairment (MCI) to dementia. Methods: We scrutinised and rated CT and MRI brain scans for degree of WML in a memory clinic cohort of 129 patients with at least 1 year of follow-up. We examined the relationship between WML severity and time until conversion to dementia for all MCI patients and for amnestic (aMCI) and non-amnestic (naMCI) subgroups separately. Results: Five-year outcome data were available for 87 (67%) of the 129 patients. The proportion of patients converting to dementia was 25% at 1 year and 76% at 5 years. Patients with aMCI converted to dementia significantly earlier than those with naMCI. WML severity was not associated with time to conversion to dementia for either MCI patients in general or aMCI patients in particular. Among naMCI patients, there was a tendency for those with a low degree of WML to survive without dementia for longer than those with a high degree of WML. However, this was not statistically significant. Conclusions: MCI subtype is a significant independent predictor of conversion to dementia, with aMCI patients having higher risk than naMCI for conversion throughout the 5-year follow-up period. WML severity does not influence conversion to dementia for aMCI but might accelerate progression in naMCI. |
format | Online Article Text |
id | pubmed-3518278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35182782013-01-28 Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? Devine, Michael E. Fonseca, J. Andres Saez Walker, Zuzana Int Psychogeriatr Research Article Background: Cerebral white matter lesions (WML), evident on CT and MRI brain scans, are histopathologically heterogeneous but associated with vascular risk factors and thought mainly to indicate ischemic damage. There has been disagreement over their clinical prognostic value in predicting conversion from mild cognitive impairment (MCI) to dementia. Methods: We scrutinised and rated CT and MRI brain scans for degree of WML in a memory clinic cohort of 129 patients with at least 1 year of follow-up. We examined the relationship between WML severity and time until conversion to dementia for all MCI patients and for amnestic (aMCI) and non-amnestic (naMCI) subgroups separately. Results: Five-year outcome data were available for 87 (67%) of the 129 patients. The proportion of patients converting to dementia was 25% at 1 year and 76% at 5 years. Patients with aMCI converted to dementia significantly earlier than those with naMCI. WML severity was not associated with time to conversion to dementia for either MCI patients in general or aMCI patients in particular. Among naMCI patients, there was a tendency for those with a low degree of WML to survive without dementia for longer than those with a high degree of WML. However, this was not statistically significant. Conclusions: MCI subtype is a significant independent predictor of conversion to dementia, with aMCI patients having higher risk than naMCI for conversion throughout the 5-year follow-up period. WML severity does not influence conversion to dementia for aMCI but might accelerate progression in naMCI. Cambridge University Press 2013-01 2012-07-03 /pmc/articles/PMC3518278/ /pubmed/22874528 http://dx.doi.org/10.1017/S1041610212000932 Text en Copyright © International Psychogeriatric Association 2012 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. The written permission of Cambridge University Press must be obtained for commercial re-use. |
spellingShingle | Research Article Devine, Michael E. Fonseca, J. Andres Saez Walker, Zuzana Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title | Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title_full | Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title_fullStr | Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title_full_unstemmed | Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title_short | Do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
title_sort | do cerebral white matter lesions influence the rate of progression from mild cognitive impairment to dementia? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518278/ https://www.ncbi.nlm.nih.gov/pubmed/22874528 http://dx.doi.org/10.1017/S1041610212000932 |
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