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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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. |
format | Online Article Text |
id | pubmed-5274594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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