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The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort
INTRODUCTION: In an attempt to capture clinically meaningful cognitive decline in early dementia, we developed the Cognitive‐Functional Composite (CFC). We investigated the CFC's sensitivity to decline in comparison to traditional clinical endpoints. METHODS: This longitudinal construct validat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164406/ https://www.ncbi.nlm.nih.gov/pubmed/32313832 http://dx.doi.org/10.1002/trc2.12020 |
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author | Jutten, Roos J. Harrison, John E. Brunner, A.J. Vreeswijk, R. van Deelen, R.A.J. de Jong, Frank Jan Opmeer, Esther M. Ritchie, Craig W. Aleman, André Scheltens, Philip Sikkes, Sietske A.M. |
author_facet | Jutten, Roos J. Harrison, John E. Brunner, A.J. Vreeswijk, R. van Deelen, R.A.J. de Jong, Frank Jan Opmeer, Esther M. Ritchie, Craig W. Aleman, André Scheltens, Philip Sikkes, Sietske A.M. |
author_sort | Jutten, Roos J. |
collection | PubMed |
description | INTRODUCTION: In an attempt to capture clinically meaningful cognitive decline in early dementia, we developed the Cognitive‐Functional Composite (CFC). We investigated the CFC's sensitivity to decline in comparison to traditional clinical endpoints. METHODS: This longitudinal construct validation study included 148 participants with subjective cognitive decline, mild cognitive impairment, or mild dementia. The CFC and traditional tests were administered at baseline, 3, 6, and 12 months. Sensitivity to change was investigated using linear mixed models and r (2) effect sizes. RESULTS: CFC scores declined over time (β = −.16, P < .001), with steepest decline observed in mild Alzheimer's dementia (β = −.25, P < .001). The CFC showed medium‐to‐large effect sizes at succeeding follow‐up points (r (2 )= .08‐.42), exhibiting greater change than the Clinical Dementia Rating scale (r (2 )= .02‐.12). Moreover, change on the CFC was significantly associated with informant reports of cognitive decline (β = .38, P < .001). DISCUSSION: By showing sensitivity to decline, the CFC could enhance the monitoring of disease progression in dementia research and clinical practice. |
format | Online Article Text |
id | pubmed-7164406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71644062020-04-20 The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort Jutten, Roos J. Harrison, John E. Brunner, A.J. Vreeswijk, R. van Deelen, R.A.J. de Jong, Frank Jan Opmeer, Esther M. Ritchie, Craig W. Aleman, André Scheltens, Philip Sikkes, Sietske A.M. Alzheimers Dement (N Y) Research Articles INTRODUCTION: In an attempt to capture clinically meaningful cognitive decline in early dementia, we developed the Cognitive‐Functional Composite (CFC). We investigated the CFC's sensitivity to decline in comparison to traditional clinical endpoints. METHODS: This longitudinal construct validation study included 148 participants with subjective cognitive decline, mild cognitive impairment, or mild dementia. The CFC and traditional tests were administered at baseline, 3, 6, and 12 months. Sensitivity to change was investigated using linear mixed models and r (2) effect sizes. RESULTS: CFC scores declined over time (β = −.16, P < .001), with steepest decline observed in mild Alzheimer's dementia (β = −.25, P < .001). The CFC showed medium‐to‐large effect sizes at succeeding follow‐up points (r (2 )= .08‐.42), exhibiting greater change than the Clinical Dementia Rating scale (r (2 )= .02‐.12). Moreover, change on the CFC was significantly associated with informant reports of cognitive decline (β = .38, P < .001). DISCUSSION: By showing sensitivity to decline, the CFC could enhance the monitoring of disease progression in dementia research and clinical practice. John Wiley and Sons Inc. 2020-04-17 /pmc/articles/PMC7164406/ /pubmed/32313832 http://dx.doi.org/10.1002/trc2.12020 Text en © 2020 The Authors. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals LLC on behalf of Alzheimer's Association This is an open access article under the terms of the 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 Jutten, Roos J. Harrison, John E. Brunner, A.J. Vreeswijk, R. van Deelen, R.A.J. de Jong, Frank Jan Opmeer, Esther M. Ritchie, Craig W. Aleman, André Scheltens, Philip Sikkes, Sietske A.M. The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title | The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title_full | The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title_fullStr | The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title_full_unstemmed | The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title_short | The Cognitive‐Functional Composite is sensitive to clinical progression in early dementia: Longitudinal findings from the Catch‐Cog study cohort |
title_sort | cognitive‐functional composite is sensitive to clinical progression in early dementia: longitudinal findings from the catch‐cog study cohort |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164406/ https://www.ncbi.nlm.nih.gov/pubmed/32313832 http://dx.doi.org/10.1002/trc2.12020 |
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