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Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change?
BACKGROUND: Post hoc analyses from clinical trials in Alzheimer's disease (AD) suggest that more cognitively impaired participants respond differently from less impaired on cognitive outcomes. We examined pooled clinical trials data to assess the utility of enriching trials using baseline cogni...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040516/ https://www.ncbi.nlm.nih.gov/pubmed/27695707 http://dx.doi.org/10.1016/j.trci.2015.03.001 |
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author | Kennedy, Richard E. Cutter, Gary R. Wang, Guoqiao Schneider, Lon S. |
author_facet | Kennedy, Richard E. Cutter, Gary R. Wang, Guoqiao Schneider, Lon S. |
author_sort | Kennedy, Richard E. |
collection | PubMed |
description | BACKGROUND: Post hoc analyses from clinical trials in Alzheimer's disease (AD) suggest that more cognitively impaired participants respond differently from less impaired on cognitive outcomes. We examined pooled clinical trials data to assess the utility of enriching trials using baseline cognition. METHODS: We included 2882 participants with mild to moderate AD in seven studies from a meta-database. We used mixed effects models to estimate the rate of decline in Alzheimer's disease Assessment Scale-cognitive (ADAS-Cog) scores among Mini-Mental State Examination (MMSE) groups. FINDINGS: Baseline MMSE category was associated with baseline scores and rate of decline on the ADAS-Cog, adjusting for age and education (both P < .001). Greater baseline cognitive impairment was associated with more rapid progression. INTERPRETATIONS: Although we found significant differences in rate of decline, most differences between individuals were from baseline ADAS-Cog values. Since enrichment based on MMSE would reduce the recruitment pool while adding only slightly to detecting differences in rate of progression, it is not advised. |
format | Online Article Text |
id | pubmed-5040516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50405162016-09-28 Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? Kennedy, Richard E. Cutter, Gary R. Wang, Guoqiao Schneider, Lon S. Alzheimers Dement (N Y) Featured Article BACKGROUND: Post hoc analyses from clinical trials in Alzheimer's disease (AD) suggest that more cognitively impaired participants respond differently from less impaired on cognitive outcomes. We examined pooled clinical trials data to assess the utility of enriching trials using baseline cognition. METHODS: We included 2882 participants with mild to moderate AD in seven studies from a meta-database. We used mixed effects models to estimate the rate of decline in Alzheimer's disease Assessment Scale-cognitive (ADAS-Cog) scores among Mini-Mental State Examination (MMSE) groups. FINDINGS: Baseline MMSE category was associated with baseline scores and rate of decline on the ADAS-Cog, adjusting for age and education (both P < .001). Greater baseline cognitive impairment was associated with more rapid progression. INTERPRETATIONS: Although we found significant differences in rate of decline, most differences between individuals were from baseline ADAS-Cog values. Since enrichment based on MMSE would reduce the recruitment pool while adding only slightly to detecting differences in rate of progression, it is not advised. Elsevier 2015-03-26 /pmc/articles/PMC5040516/ /pubmed/27695707 http://dx.doi.org/10.1016/j.trci.2015.03.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Featured Article Kennedy, Richard E. Cutter, Gary R. Wang, Guoqiao Schneider, Lon S. Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title | Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title_full | Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title_fullStr | Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title_full_unstemmed | Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title_short | Using baseline cognitive severity for enriching Alzheimer's disease clinical trials: How does Mini-Mental State Examination predict rate of change? |
title_sort | using baseline cognitive severity for enriching alzheimer's disease clinical trials: how does mini-mental state examination predict rate of change? |
topic | Featured Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040516/ https://www.ncbi.nlm.nih.gov/pubmed/27695707 http://dx.doi.org/10.1016/j.trci.2015.03.001 |
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