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Power and sample size calculations for comparison of two regression lines with heterogeneous variances

The existence of interactive effects of a dichotomous treatment variable on the relationship between the continuous predictor and response variables is an essential issue in biological and medical sciences. Also, considerable attention has been devoted to raising awareness of the often-untenable ass...

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Autor principal: Shieh, Gwowen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296670/
https://www.ncbi.nlm.nih.gov/pubmed/30557387
http://dx.doi.org/10.1371/journal.pone.0207745
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author Shieh, Gwowen
author_facet Shieh, Gwowen
author_sort Shieh, Gwowen
collection PubMed
description The existence of interactive effects of a dichotomous treatment variable on the relationship between the continuous predictor and response variables is an essential issue in biological and medical sciences. Also, considerable attention has been devoted to raising awareness of the often-untenable assumption of homogeneous error variance among treatment groups. Although the procedures for detecting interactions between treatment and predictor variables are well documented in the literature, the corresponding problem of power and sample size calculations has received relatively little attention. In order to facilitate interaction design planning, this article describes power and sample size procedures for the extended Welch test of difference between two regression slopes under heterogeneity of variance. Two different formulations are presented to explicate the implications of appropriate reliance on the predictor variables. The simplified method only utilizes the partial information of predictor variances and has the advantages of statistical and computational simplifications. However, extensive numerical investigations showed that it is relatively less accurate than the more profound procedure that accommodates the full distributional features of the predictors. According to the analytic justification and empirical performance, the proposed approach gives reliable solutions to power assessment and sample size determination in the detection of interaction effects. A numerical example involving kidney weigh and body weigh of crossbred diabetic and normal mice is used to illustrate the suggested procedures with flexible allocation schemes. Moreover, the organ and body weights data is incorporated in the accompany SAS and R software programs to illustrate the ease and convenience of the proposed techniques for design planning in interactive research.
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spelling pubmed-62966702018-12-28 Power and sample size calculations for comparison of two regression lines with heterogeneous variances Shieh, Gwowen PLoS One Research Article The existence of interactive effects of a dichotomous treatment variable on the relationship between the continuous predictor and response variables is an essential issue in biological and medical sciences. Also, considerable attention has been devoted to raising awareness of the often-untenable assumption of homogeneous error variance among treatment groups. Although the procedures for detecting interactions between treatment and predictor variables are well documented in the literature, the corresponding problem of power and sample size calculations has received relatively little attention. In order to facilitate interaction design planning, this article describes power and sample size procedures for the extended Welch test of difference between two regression slopes under heterogeneity of variance. Two different formulations are presented to explicate the implications of appropriate reliance on the predictor variables. The simplified method only utilizes the partial information of predictor variances and has the advantages of statistical and computational simplifications. However, extensive numerical investigations showed that it is relatively less accurate than the more profound procedure that accommodates the full distributional features of the predictors. According to the analytic justification and empirical performance, the proposed approach gives reliable solutions to power assessment and sample size determination in the detection of interaction effects. A numerical example involving kidney weigh and body weigh of crossbred diabetic and normal mice is used to illustrate the suggested procedures with flexible allocation schemes. Moreover, the organ and body weights data is incorporated in the accompany SAS and R software programs to illustrate the ease and convenience of the proposed techniques for design planning in interactive research. Public Library of Science 2018-12-17 /pmc/articles/PMC6296670/ /pubmed/30557387 http://dx.doi.org/10.1371/journal.pone.0207745 Text en © 2018 Gwowen Shieh http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shieh, Gwowen
Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title_full Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title_fullStr Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title_full_unstemmed Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title_short Power and sample size calculations for comparison of two regression lines with heterogeneous variances
title_sort power and sample size calculations for comparison of two regression lines with heterogeneous variances
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296670/
https://www.ncbi.nlm.nih.gov/pubmed/30557387
http://dx.doi.org/10.1371/journal.pone.0207745
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