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Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population
BACKGROUND: Down’s syndrome (DS) is the most common genetic cause of intellectual disability. People with DS are at an increased risk of Alzheimer’s disease (AD) compared to the general population. Neuroimaging studies of AD have focused on medial temporal structures; however, to our knowledge, no i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765707/ https://www.ncbi.nlm.nih.gov/pubmed/23962297 http://dx.doi.org/10.1186/1866-1955-5-19 |
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author | Mullins, Diane Daly, Eileen Simmons, Andrew Beacher, Felix Foy, Catherine ML Lovestone, Simon Hallahan, Brian Murphy, Kieran C Murphy, Declan G |
author_facet | Mullins, Diane Daly, Eileen Simmons, Andrew Beacher, Felix Foy, Catherine ML Lovestone, Simon Hallahan, Brian Murphy, Kieran C Murphy, Declan G |
author_sort | Mullins, Diane |
collection | PubMed |
description | BACKGROUND: Down’s syndrome (DS) is the most common genetic cause of intellectual disability. People with DS are at an increased risk of Alzheimer’s disease (AD) compared to the general population. Neuroimaging studies of AD have focused on medial temporal structures; however, to our knowledge, no in vivo case–control study exists comparing the anatomy of dementia in DS to people with AD in the general population. We therefore compared the in vivo brain anatomy of people with DS and dementia (DS+) to those with AD in the general population. METHOD: Using MRI in 192 adults, we compared the volume of whole brain matter, lateral ventricles, temporal lobes and hippocampus in DS subjects with and without dementia (DS+, DS-), to each other and to three non-DS groups. These included one group of individuals with AD and two groups of controls (each age-matched for their respective DS and general population AD cohorts). RESULTS: AD and DS+ subjects showed significant reductions in the volume of the whole brain, hippocampus and temporal lobes and a significant elevation in the volume of the lateral ventricle, compared to their non-demented counterparts. People with DS+ had a smaller reduction in temporal lobe volume compared to individuals with AD. CONCLUSIONS: DS+ and AD subjects have a significant reduction in volume of the same brain regions. We found preliminary evidence that DS individuals may be more sensitive to tissue loss than others and have less ‘cognitive reserve’. |
format | Online Article Text |
id | pubmed-3765707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37657072013-09-08 Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population Mullins, Diane Daly, Eileen Simmons, Andrew Beacher, Felix Foy, Catherine ML Lovestone, Simon Hallahan, Brian Murphy, Kieran C Murphy, Declan G J Neurodev Disord Research BACKGROUND: Down’s syndrome (DS) is the most common genetic cause of intellectual disability. People with DS are at an increased risk of Alzheimer’s disease (AD) compared to the general population. Neuroimaging studies of AD have focused on medial temporal structures; however, to our knowledge, no in vivo case–control study exists comparing the anatomy of dementia in DS to people with AD in the general population. We therefore compared the in vivo brain anatomy of people with DS and dementia (DS+) to those with AD in the general population. METHOD: Using MRI in 192 adults, we compared the volume of whole brain matter, lateral ventricles, temporal lobes and hippocampus in DS subjects with and without dementia (DS+, DS-), to each other and to three non-DS groups. These included one group of individuals with AD and two groups of controls (each age-matched for their respective DS and general population AD cohorts). RESULTS: AD and DS+ subjects showed significant reductions in the volume of the whole brain, hippocampus and temporal lobes and a significant elevation in the volume of the lateral ventricle, compared to their non-demented counterparts. People with DS+ had a smaller reduction in temporal lobe volume compared to individuals with AD. CONCLUSIONS: DS+ and AD subjects have a significant reduction in volume of the same brain regions. We found preliminary evidence that DS individuals may be more sensitive to tissue loss than others and have less ‘cognitive reserve’. BioMed Central 2013 2013-08-20 /pmc/articles/PMC3765707/ /pubmed/23962297 http://dx.doi.org/10.1186/1866-1955-5-19 Text en Copyright © 2013 Mullins et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Mullins, Diane Daly, Eileen Simmons, Andrew Beacher, Felix Foy, Catherine ML Lovestone, Simon Hallahan, Brian Murphy, Kieran C Murphy, Declan G Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title | Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title_full | Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title_fullStr | Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title_full_unstemmed | Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title_short | Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population |
title_sort | dementia in down’s syndrome: an mri comparison with alzheimer’s disease in the general population |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765707/ https://www.ncbi.nlm.nih.gov/pubmed/23962297 http://dx.doi.org/10.1186/1866-1955-5-19 |
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