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The natural history of early-onset dementia: the Artemis Project

OBJECTIVES: The natural history of early-onset Alzheimer's disease (AD) and fronto-temporal dementia (FTD) remains to be described in detail. We seek to describe the natural history of early onset AD and FTD in terms of changes in cognitive assessment and staging, medical history and survival....

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Autores principales: Atkins, Emily R, Bulsara, Max K, Panegyres, Peter K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488731/
https://www.ncbi.nlm.nih.gov/pubmed/23059847
http://dx.doi.org/10.1136/bmjopen-2012-001764
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author Atkins, Emily R
Bulsara, Max K
Panegyres, Peter K
author_facet Atkins, Emily R
Bulsara, Max K
Panegyres, Peter K
author_sort Atkins, Emily R
collection PubMed
description OBJECTIVES: The natural history of early-onset Alzheimer's disease (AD) and fronto-temporal dementia (FTD) remains to be described in detail. We seek to describe the natural history of early onset AD and FTD in terms of changes in cognitive assessment and staging, medical history and survival. DESIGN: Longitudinal prospective cohort analysis. SETTING: Neurodegenerative disorders research clinic. PARTICIPANTS: In total, 155 consecutive patients with clinically confirmed sporadic early-onset AD or FTD at a neurodegenerative disorders research clinic in Subiaco, Western Australia (The Artemis Project). METHODS: A detailed history was recorded from the patients at baseline, including education, family history and medical history. Mini-mental state exam (MMSE), Global Deterioration Scale (GDS) and total functional capacity (TFC) were determined at each visit from 1994 until 2011. Kaplan-Meier survival analysis was performed. RESULTS: Patients with FTD were more likely to have a family history of dementia (p=0.026), to develop at least one cerebrovascular risk factor (p=0.003), manifest depression (Fisher's exact p=0.007) and to die during the follow-up period (Pearson χ(2) 8.97, p=0.003). Kaplan-Meier survival estimates revealed a highly significant difference in the proportion of patients surviving the follow-up period (log rank 7.25, p=0.007) with FTD patients experiencing poorer survival than those with AD. The mean MMSE and TFC were consistently lower in those with FTD compared with those with AD over a decade of follow-up; mean GDS was consistently higher in those with FTD over the follow-up period. CONCLUSIONS: We believe that the difference in survival in patients with AD and FTD in our cohort might relate to the development of one or more cerebrovascular risk factors in FTD patients and the severity of the underlying pathology.
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spelling pubmed-34887312012-11-05 The natural history of early-onset dementia: the Artemis Project Atkins, Emily R Bulsara, Max K Panegyres, Peter K BMJ Open Neurology OBJECTIVES: The natural history of early-onset Alzheimer's disease (AD) and fronto-temporal dementia (FTD) remains to be described in detail. We seek to describe the natural history of early onset AD and FTD in terms of changes in cognitive assessment and staging, medical history and survival. DESIGN: Longitudinal prospective cohort analysis. SETTING: Neurodegenerative disorders research clinic. PARTICIPANTS: In total, 155 consecutive patients with clinically confirmed sporadic early-onset AD or FTD at a neurodegenerative disorders research clinic in Subiaco, Western Australia (The Artemis Project). METHODS: A detailed history was recorded from the patients at baseline, including education, family history and medical history. Mini-mental state exam (MMSE), Global Deterioration Scale (GDS) and total functional capacity (TFC) were determined at each visit from 1994 until 2011. Kaplan-Meier survival analysis was performed. RESULTS: Patients with FTD were more likely to have a family history of dementia (p=0.026), to develop at least one cerebrovascular risk factor (p=0.003), manifest depression (Fisher's exact p=0.007) and to die during the follow-up period (Pearson χ(2) 8.97, p=0.003). Kaplan-Meier survival estimates revealed a highly significant difference in the proportion of patients surviving the follow-up period (log rank 7.25, p=0.007) with FTD patients experiencing poorer survival than those with AD. The mean MMSE and TFC were consistently lower in those with FTD compared with those with AD over a decade of follow-up; mean GDS was consistently higher in those with FTD over the follow-up period. CONCLUSIONS: We believe that the difference in survival in patients with AD and FTD in our cohort might relate to the development of one or more cerebrovascular risk factors in FTD patients and the severity of the underlying pathology. BMJ Publishing Group 2012 2012-10-10 /pmc/articles/PMC3488731/ /pubmed/23059847 http://dx.doi.org/10.1136/bmjopen-2012-001764 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Neurology
Atkins, Emily R
Bulsara, Max K
Panegyres, Peter K
The natural history of early-onset dementia: the Artemis Project
title The natural history of early-onset dementia: the Artemis Project
title_full The natural history of early-onset dementia: the Artemis Project
title_fullStr The natural history of early-onset dementia: the Artemis Project
title_full_unstemmed The natural history of early-onset dementia: the Artemis Project
title_short The natural history of early-onset dementia: the Artemis Project
title_sort natural history of early-onset dementia: the artemis project
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488731/
https://www.ncbi.nlm.nih.gov/pubmed/23059847
http://dx.doi.org/10.1136/bmjopen-2012-001764
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