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A comparison of methods to adjust for continuous covariates in the analysis of randomised trials
BACKGROUND: Although covariate adjustment in the analysis of randomised trials can be beneficial, adjustment for continuous covariates is complicated by the fact that the association between covariate and outcome must be specified. Misspecification of this association can lead to reduced power, and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827223/ https://www.ncbi.nlm.nih.gov/pubmed/27068456 http://dx.doi.org/10.1186/s12874-016-0141-3 |
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author | Kahan, Brennan C. Rushton, Helen Morris, Tim P. Daniel, Rhian M. |
author_facet | Kahan, Brennan C. Rushton, Helen Morris, Tim P. Daniel, Rhian M. |
author_sort | Kahan, Brennan C. |
collection | PubMed |
description | BACKGROUND: Although covariate adjustment in the analysis of randomised trials can be beneficial, adjustment for continuous covariates is complicated by the fact that the association between covariate and outcome must be specified. Misspecification of this association can lead to reduced power, and potentially incorrect conclusions regarding treatment efficacy. METHODS: We compared several methods of adjustment to determine which is best when the association between covariate and outcome is unknown. We assessed (a) dichotomisation or categorisation; (b) assuming a linear association with outcome; (c) using fractional polynomials with one (FP1) or two (FP2) polynomial terms; and (d) using restricted cubic splines with 3 or 5 knots. We evaluated each method using simulation and through a re-analysis of trial datasets. RESULTS: Methods which kept covariates as continuous typically had higher power than methods which used categorisation. Dichotomisation, categorisation, and assuming a linear association all led to large reductions in power when the true association was non-linear. FP2 models and restricted cubic splines with 3 or 5 knots performed best overall. CONCLUSIONS: For the analysis of randomised trials we recommend (1) adjusting for continuous covariates even if their association with outcome is unknown; (2) keeping covariates as continuous; and (3) using fractional polynomials with two polynomial terms or restricted cubic splines with 3 to 5 knots when a linear association is in doubt. |
format | Online Article Text |
id | pubmed-4827223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48272232016-04-12 A comparison of methods to adjust for continuous covariates in the analysis of randomised trials Kahan, Brennan C. Rushton, Helen Morris, Tim P. Daniel, Rhian M. BMC Med Res Methodol Research Article BACKGROUND: Although covariate adjustment in the analysis of randomised trials can be beneficial, adjustment for continuous covariates is complicated by the fact that the association between covariate and outcome must be specified. Misspecification of this association can lead to reduced power, and potentially incorrect conclusions regarding treatment efficacy. METHODS: We compared several methods of adjustment to determine which is best when the association between covariate and outcome is unknown. We assessed (a) dichotomisation or categorisation; (b) assuming a linear association with outcome; (c) using fractional polynomials with one (FP1) or two (FP2) polynomial terms; and (d) using restricted cubic splines with 3 or 5 knots. We evaluated each method using simulation and through a re-analysis of trial datasets. RESULTS: Methods which kept covariates as continuous typically had higher power than methods which used categorisation. Dichotomisation, categorisation, and assuming a linear association all led to large reductions in power when the true association was non-linear. FP2 models and restricted cubic splines with 3 or 5 knots performed best overall. CONCLUSIONS: For the analysis of randomised trials we recommend (1) adjusting for continuous covariates even if their association with outcome is unknown; (2) keeping covariates as continuous; and (3) using fractional polynomials with two polynomial terms or restricted cubic splines with 3 to 5 knots when a linear association is in doubt. BioMed Central 2016-04-11 /pmc/articles/PMC4827223/ /pubmed/27068456 http://dx.doi.org/10.1186/s12874-016-0141-3 Text en © Kahan et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kahan, Brennan C. Rushton, Helen Morris, Tim P. Daniel, Rhian M. A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title | A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title_full | A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title_fullStr | A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title_full_unstemmed | A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title_short | A comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
title_sort | comparison of methods to adjust for continuous covariates in the analysis of randomised trials |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827223/ https://www.ncbi.nlm.nih.gov/pubmed/27068456 http://dx.doi.org/10.1186/s12874-016-0141-3 |
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