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Quantifying temporal trends of age-standardized rates with odds

BACKGROUND: To quantify temporal trends in age-standardized rates of disease, the convention is to fit a linear regression model to log-transformed rates because the slope term provides the estimated annual percentage change. However, such log-transformation is not always appropriate. METHODS: We pr...

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Autores principales: Tan, Chuen Seng, Støer, Nathalie, Ning, Yilin, Chen, Ying, Reilly, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299543/
https://www.ncbi.nlm.nih.gov/pubmed/30563536
http://dx.doi.org/10.1186/s12963-018-0173-5
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author Tan, Chuen Seng
Støer, Nathalie
Ning, Yilin
Chen, Ying
Reilly, Marie
author_facet Tan, Chuen Seng
Støer, Nathalie
Ning, Yilin
Chen, Ying
Reilly, Marie
author_sort Tan, Chuen Seng
collection PubMed
description BACKGROUND: To quantify temporal trends in age-standardized rates of disease, the convention is to fit a linear regression model to log-transformed rates because the slope term provides the estimated annual percentage change. However, such log-transformation is not always appropriate. METHODS: We propose an alternative method using the rank-ordered logit (ROL) model that is indifferent to log-transformation. This method quantifies the temporal trend using odds, a quantity commonly used in epidemiology, and the log-odds corresponds to the scaled slope parameter estimate from linear regression. The ROL method can be implemented by using the commands for proportional hazards regression in any standard statistical package. We apply the ROL method to estimate temporal trends in age-standardized cancer rates worldwide using the cancer incidence data from the Cancer Incidence in Five Continents plus (CI5plus) database for the period 1953 to 2007 and compare the estimates to their scaled counterparts obtained from linear regression with and without log-transformation. RESULTS: We found a strong concordance in the direction and significance of the temporal trends in cancer incidence estimated by all three approaches, and illustrated how the estimate from the ROL model provides a measure that is comparable to a scaled slope parameter estimated from linear regression. CONCLUSIONS: Our method offers an alternative approach for quantifying temporal trends in incidence or mortality rates in a population that is invariant to transformation, and whose estimate of trend agrees with the scaled slope from a linear regression model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12963-018-0173-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-62995432018-12-20 Quantifying temporal trends of age-standardized rates with odds Tan, Chuen Seng Støer, Nathalie Ning, Yilin Chen, Ying Reilly, Marie Popul Health Metr Research BACKGROUND: To quantify temporal trends in age-standardized rates of disease, the convention is to fit a linear regression model to log-transformed rates because the slope term provides the estimated annual percentage change. However, such log-transformation is not always appropriate. METHODS: We propose an alternative method using the rank-ordered logit (ROL) model that is indifferent to log-transformation. This method quantifies the temporal trend using odds, a quantity commonly used in epidemiology, and the log-odds corresponds to the scaled slope parameter estimate from linear regression. The ROL method can be implemented by using the commands for proportional hazards regression in any standard statistical package. We apply the ROL method to estimate temporal trends in age-standardized cancer rates worldwide using the cancer incidence data from the Cancer Incidence in Five Continents plus (CI5plus) database for the period 1953 to 2007 and compare the estimates to their scaled counterparts obtained from linear regression with and without log-transformation. RESULTS: We found a strong concordance in the direction and significance of the temporal trends in cancer incidence estimated by all three approaches, and illustrated how the estimate from the ROL model provides a measure that is comparable to a scaled slope parameter estimated from linear regression. CONCLUSIONS: Our method offers an alternative approach for quantifying temporal trends in incidence or mortality rates in a population that is invariant to transformation, and whose estimate of trend agrees with the scaled slope from a linear regression model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12963-018-0173-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-18 /pmc/articles/PMC6299543/ /pubmed/30563536 http://dx.doi.org/10.1186/s12963-018-0173-5 Text en © The Author(s). 2018 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
Tan, Chuen Seng
Støer, Nathalie
Ning, Yilin
Chen, Ying
Reilly, Marie
Quantifying temporal trends of age-standardized rates with odds
title Quantifying temporal trends of age-standardized rates with odds
title_full Quantifying temporal trends of age-standardized rates with odds
title_fullStr Quantifying temporal trends of age-standardized rates with odds
title_full_unstemmed Quantifying temporal trends of age-standardized rates with odds
title_short Quantifying temporal trends of age-standardized rates with odds
title_sort quantifying temporal trends of age-standardized rates with odds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299543/
https://www.ncbi.nlm.nih.gov/pubmed/30563536
http://dx.doi.org/10.1186/s12963-018-0173-5
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