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Statistical analysis of longitudinal data on tumour growth in mice experiments
We consider mice experiments where tumour cells are injected so that a tumour starts to grow. When the tumour reaches a certain volume, mice are randomized into treatment groups. Tumour volume is measured repeatedly until the mouse dies or is sacrificed. Tumour growth rates are compared between grou...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272435/ https://www.ncbi.nlm.nih.gov/pubmed/32499558 http://dx.doi.org/10.1038/s41598-020-65767-7 |
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author | Zavrakidis, Ioannis Jóźwiak, Katarzyna Hauptmann, Michael |
author_facet | Zavrakidis, Ioannis Jóźwiak, Katarzyna Hauptmann, Michael |
author_sort | Zavrakidis, Ioannis |
collection | PubMed |
description | We consider mice experiments where tumour cells are injected so that a tumour starts to grow. When the tumour reaches a certain volume, mice are randomized into treatment groups. Tumour volume is measured repeatedly until the mouse dies or is sacrificed. Tumour growth rates are compared between groups. We propose and evaluate linear regression for analysis accounting for the correlation among repeated measurements per mouse. More specifically, we examined five models with three different variance-covariance structures in order to recommend the least complex method for small to moderate sample sizes encountered in animal experiments. We performed a simulation study based on data from three previous experiments to investigate the properties of estimates of the difference between treatment groups. Models were estimated via marginal modelling using generalized least squares and restricted maximum likelihood estimation. A model with an autoregressive (AR-1) covariance structure was efficient and unbiased retaining nominal coverage and type I error when the AR-1 variance-covariance matrix correctly specified the association between repeated measurements. When the variance-covariance was misspecified, that model was still unbiased but the type I error and the coverage rates were affected depending on the degree of misspecification. A linear regression model with an autoregressive (AR-1) covariance structure is an adequate model to analyse experiments that compare tumour growth rates between treatment groups. |
format | Online Article Text |
id | pubmed-7272435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72724352020-06-05 Statistical analysis of longitudinal data on tumour growth in mice experiments Zavrakidis, Ioannis Jóźwiak, Katarzyna Hauptmann, Michael Sci Rep Article We consider mice experiments where tumour cells are injected so that a tumour starts to grow. When the tumour reaches a certain volume, mice are randomized into treatment groups. Tumour volume is measured repeatedly until the mouse dies or is sacrificed. Tumour growth rates are compared between groups. We propose and evaluate linear regression for analysis accounting for the correlation among repeated measurements per mouse. More specifically, we examined five models with three different variance-covariance structures in order to recommend the least complex method for small to moderate sample sizes encountered in animal experiments. We performed a simulation study based on data from three previous experiments to investigate the properties of estimates of the difference between treatment groups. Models were estimated via marginal modelling using generalized least squares and restricted maximum likelihood estimation. A model with an autoregressive (AR-1) covariance structure was efficient and unbiased retaining nominal coverage and type I error when the AR-1 variance-covariance matrix correctly specified the association between repeated measurements. When the variance-covariance was misspecified, that model was still unbiased but the type I error and the coverage rates were affected depending on the degree of misspecification. A linear regression model with an autoregressive (AR-1) covariance structure is an adequate model to analyse experiments that compare tumour growth rates between treatment groups. Nature Publishing Group UK 2020-06-04 /pmc/articles/PMC7272435/ /pubmed/32499558 http://dx.doi.org/10.1038/s41598-020-65767-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zavrakidis, Ioannis Jóźwiak, Katarzyna Hauptmann, Michael Statistical analysis of longitudinal data on tumour growth in mice experiments |
title | Statistical analysis of longitudinal data on tumour growth in mice experiments |
title_full | Statistical analysis of longitudinal data on tumour growth in mice experiments |
title_fullStr | Statistical analysis of longitudinal data on tumour growth in mice experiments |
title_full_unstemmed | Statistical analysis of longitudinal data on tumour growth in mice experiments |
title_short | Statistical analysis of longitudinal data on tumour growth in mice experiments |
title_sort | statistical analysis of longitudinal data on tumour growth in mice experiments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272435/ https://www.ncbi.nlm.nih.gov/pubmed/32499558 http://dx.doi.org/10.1038/s41598-020-65767-7 |
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