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Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies

A recent article by Schneider and colleagues has generated a lot of interest in simulation studies as a way to improve study design. The study also illustrates the foremost principal in simulation studies, which is that the results of a simulation are an embodiment of the assumptions that went into...

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Autor principal: Hendrix, Suzanne B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226272/
https://www.ncbi.nlm.nih.gov/pubmed/21457497
http://dx.doi.org/10.1186/alzrt69
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author Hendrix, Suzanne B
author_facet Hendrix, Suzanne B
author_sort Hendrix, Suzanne B
collection PubMed
description A recent article by Schneider and colleagues has generated a lot of interest in simulation studies as a way to improve study design. The study also illustrates the foremost principal in simulation studies, which is that the results of a simulation are an embodiment of the assumptions that went into it. This simulation study assumes that the effect size is proportional to the mean to standard deviation ratio of the Alzheimer Disease Assessment Scale - cognitive subscale in the population being studied. Under this assumption, selecting a subgroup for a clinical trial based on biomarkers will not affect the efficiency of the study, despite achieving the desired increase in the mean to standard deviation ratio.
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spelling pubmed-32262722011-11-30 Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies Hendrix, Suzanne B Alzheimers Res Ther Viewpoint A recent article by Schneider and colleagues has generated a lot of interest in simulation studies as a way to improve study design. The study also illustrates the foremost principal in simulation studies, which is that the results of a simulation are an embodiment of the assumptions that went into it. This simulation study assumes that the effect size is proportional to the mean to standard deviation ratio of the Alzheimer Disease Assessment Scale - cognitive subscale in the population being studied. Under this assumption, selecting a subgroup for a clinical trial based on biomarkers will not affect the efficiency of the study, despite achieving the desired increase in the mean to standard deviation ratio. BioMed Central 2011-03-28 /pmc/articles/PMC3226272/ /pubmed/21457497 http://dx.doi.org/10.1186/alzrt69 Text en Copyright ©2011 BioMed Central Ltd
spellingShingle Viewpoint
Hendrix, Suzanne B
Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title_full Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title_fullStr Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title_full_unstemmed Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title_short Requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
title_sort requiring an amyloid-β(1-42 )biomarker may improve the efficiency of a study, and simulations may help in planning studies
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226272/
https://www.ncbi.nlm.nih.gov/pubmed/21457497
http://dx.doi.org/10.1186/alzrt69
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