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Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia

OBJECTIVE: To investigate the psychometric properties of the Clinical Dementia Scale—frontotemporal lobar degeneration (CDR‐FTLD) psychometric properties using Rasch analysis and its sensitivity distinguishing disease progression between FTLD and Alzheimer's disease (AD). METHODS: Of 603 consec...

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Autores principales: Mioshi, Eneida, Flanagan, Emma, Knopman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274594/
https://www.ncbi.nlm.nih.gov/pubmed/27464599
http://dx.doi.org/10.1002/gps.4556
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author Mioshi, Eneida
Flanagan, Emma
Knopman, David
author_facet Mioshi, Eneida
Flanagan, Emma
Knopman, David
author_sort Mioshi, Eneida
collection PubMed
description OBJECTIVE: To investigate the psychometric properties of the Clinical Dementia Scale—frontotemporal lobar degeneration (CDR‐FTLD) psychometric properties using Rasch analysis and its sensitivity distinguishing disease progression between FTLD and Alzheimer's disease (AD). METHODS: Of 603 consecutive patients from the National Alzheimer Coordinating Center dataset (FTLD = 350; AD = 253), 120 FTLDs were included in a Rasch analysis to verify CDR‐FTLD psychometric properties; 483 (FTLD = 230; AD = 253) were included to analyse disease progression, with 195 (FTLD = 82; AD = 113) followed‐up (24 months). RESULTS: The CDR‐FTLD demonstrated good consistency, construct and concurrent validity and correlated well with mini‐mental state examination (MMSE) and disease duration (ps < 0.05). At baseline, FTLD showed greater dementia severity than AD after matched for MMSE and disease duration (p < 0.001). Independent Rasch analyses demonstrated different patterns of progression for FTLD and AD in terms of the domains initially and then subsequently affected with disease progression. At follow‐up, although MMSE showed significant changes (p < 0.05), these were greater on the CDR‐FTLD (p < 0.001). CONCLUSION: The CDR‐FTLD satisfactorily measures dementia severity and change in FTLD, distinguishing disease progression between FTLD and AD, with clear implications for care, prognosis and future clinical trials. © 2016 The Authors. International Journal of Geriatric Psychiatry published by John Wiley & Sons, Ltd.
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spelling pubmed-52745942017-09-01 Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia Mioshi, Eneida Flanagan, Emma Knopman, David Int J Geriatr Psychiatry Research Articles OBJECTIVE: To investigate the psychometric properties of the Clinical Dementia Scale—frontotemporal lobar degeneration (CDR‐FTLD) psychometric properties using Rasch analysis and its sensitivity distinguishing disease progression between FTLD and Alzheimer's disease (AD). METHODS: Of 603 consecutive patients from the National Alzheimer Coordinating Center dataset (FTLD = 350; AD = 253), 120 FTLDs were included in a Rasch analysis to verify CDR‐FTLD psychometric properties; 483 (FTLD = 230; AD = 253) were included to analyse disease progression, with 195 (FTLD = 82; AD = 113) followed‐up (24 months). RESULTS: The CDR‐FTLD demonstrated good consistency, construct and concurrent validity and correlated well with mini‐mental state examination (MMSE) and disease duration (ps < 0.05). At baseline, FTLD showed greater dementia severity than AD after matched for MMSE and disease duration (p < 0.001). Independent Rasch analyses demonstrated different patterns of progression for FTLD and AD in terms of the domains initially and then subsequently affected with disease progression. At follow‐up, although MMSE showed significant changes (p < 0.05), these were greater on the CDR‐FTLD (p < 0.001). CONCLUSION: The CDR‐FTLD satisfactorily measures dementia severity and change in FTLD, distinguishing disease progression between FTLD and AD, with clear implications for care, prognosis and future clinical trials. © 2016 The Authors. International Journal of Geriatric Psychiatry published by John Wiley & Sons, Ltd. John Wiley and Sons Inc. 2016-07-28 2017-09 /pmc/articles/PMC5274594/ /pubmed/27464599 http://dx.doi.org/10.1002/gps.4556 Text en © 2016 The Authors. International Journal of Geriatric Psychiatry published by John Wiley & Sons, Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Mioshi, Eneida
Flanagan, Emma
Knopman, David
Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title_full Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title_fullStr Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title_full_unstemmed Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title_short Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
title_sort detecting clinical change with the cdr‐ftld: differences between ftld and ad dementia
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274594/
https://www.ncbi.nlm.nih.gov/pubmed/27464599
http://dx.doi.org/10.1002/gps.4556
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