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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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