Cargando…

Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues

This paper examines how to reduce the number of control animals in preclinical hyperinsulemic glucose clamp studies if we make use of information on historical studies. A dataset consisting of 59 studies in rats to investigate new insulin analogues for diabetics, collected in the years 2000 to 2015,...

Descripción completa

Detalles Bibliográficos
Autores principales: Nielsen, Emilie Prang, Andersen, Søren, Brand, Christian Lehn, Ditlevsen, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202954/
https://www.ncbi.nlm.nih.gov/pubmed/35709155
http://dx.doi.org/10.1371/journal.pone.0257750
_version_ 1784728625976705024
author Nielsen, Emilie Prang
Andersen, Søren
Brand, Christian Lehn
Ditlevsen, Susanne
author_facet Nielsen, Emilie Prang
Andersen, Søren
Brand, Christian Lehn
Ditlevsen, Susanne
author_sort Nielsen, Emilie Prang
collection PubMed
description This paper examines how to reduce the number of control animals in preclinical hyperinsulemic glucose clamp studies if we make use of information on historical studies. A dataset consisting of 59 studies in rats to investigate new insulin analogues for diabetics, collected in the years 2000 to 2015, is analysed. A simulation experiment is performed based on a carefully built nonlinear mixed-effects model including historical information, comparing results (for the relative log-potency) with the standard approach ignoring previous studies. We find that by including historical information in the form of the mixed-effects model proposed, we can to remove between 23% and 51% of the control rats in the two studies looked closely upon to get the same level of precision on the relative log-potency as in the standard analysis. How to incorporate the historical information in the form of the mixed-effects model is discussed, where both a mixed-effect meta-analysis approach as well as a Bayesian approach are suggested. The conclusions are similar for the two approaches, and therefore, we conclude that the inclusion of historical information is beneficial in regard to using fewer control rats.
format Online
Article
Text
id pubmed-9202954
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-92029542022-06-17 Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues Nielsen, Emilie Prang Andersen, Søren Brand, Christian Lehn Ditlevsen, Susanne PLoS One Research Article This paper examines how to reduce the number of control animals in preclinical hyperinsulemic glucose clamp studies if we make use of information on historical studies. A dataset consisting of 59 studies in rats to investigate new insulin analogues for diabetics, collected in the years 2000 to 2015, is analysed. A simulation experiment is performed based on a carefully built nonlinear mixed-effects model including historical information, comparing results (for the relative log-potency) with the standard approach ignoring previous studies. We find that by including historical information in the form of the mixed-effects model proposed, we can to remove between 23% and 51% of the control rats in the two studies looked closely upon to get the same level of precision on the relative log-potency as in the standard analysis. How to incorporate the historical information in the form of the mixed-effects model is discussed, where both a mixed-effect meta-analysis approach as well as a Bayesian approach are suggested. The conclusions are similar for the two approaches, and therefore, we conclude that the inclusion of historical information is beneficial in regard to using fewer control rats. Public Library of Science 2022-06-16 /pmc/articles/PMC9202954/ /pubmed/35709155 http://dx.doi.org/10.1371/journal.pone.0257750 Text en © 2022 Nielsen et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Nielsen, Emilie Prang
Andersen, Søren
Brand, Christian Lehn
Ditlevsen, Susanne
Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title_full Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title_fullStr Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title_full_unstemmed Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title_short Applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
title_sort applying historical data in a nonlinear mixed-effects model can reduce the number of control rats required for calculation of the relative potency of insulin analogues
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202954/
https://www.ncbi.nlm.nih.gov/pubmed/35709155
http://dx.doi.org/10.1371/journal.pone.0257750
work_keys_str_mv AT nielsenemilieprang applyinghistoricaldatainanonlinearmixedeffectsmodelcanreducethenumberofcontrolratsrequiredforcalculationoftherelativepotencyofinsulinanalogues
AT andersensøren applyinghistoricaldatainanonlinearmixedeffectsmodelcanreducethenumberofcontrolratsrequiredforcalculationoftherelativepotencyofinsulinanalogues
AT brandchristianlehn applyinghistoricaldatainanonlinearmixedeffectsmodelcanreducethenumberofcontrolratsrequiredforcalculationoftherelativepotencyofinsulinanalogues
AT ditlevsensusanne applyinghistoricaldatainanonlinearmixedeffectsmodelcanreducethenumberofcontrolratsrequiredforcalculationoftherelativepotencyofinsulinanalogues