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A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies

BACKGROUND: Case-crossover studies have been widely used in various fields including pharmacoepidemiology. Vines and Farrington indicated in 2001 that when within-subject exposure dependency exists, conditional logistic regression can be biased. However, this bias has not been well studied. METHODS:...

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Autores principales: Kubota, Kiyoshi, Kelly, Thu-Lan, Sato, Tsugumichi, Pratt, Nicole, Roughead, Elizabeth, Yamaguchi, Takuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520620/
https://www.ncbi.nlm.nih.gov/pubmed/34657592
http://dx.doi.org/10.1186/s12874-021-01408-5
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author Kubota, Kiyoshi
Kelly, Thu-Lan
Sato, Tsugumichi
Pratt, Nicole
Roughead, Elizabeth
Yamaguchi, Takuhiro
author_facet Kubota, Kiyoshi
Kelly, Thu-Lan
Sato, Tsugumichi
Pratt, Nicole
Roughead, Elizabeth
Yamaguchi, Takuhiro
author_sort Kubota, Kiyoshi
collection PubMed
description BACKGROUND: Case-crossover studies have been widely used in various fields including pharmacoepidemiology. Vines and Farrington indicated in 2001 that when within-subject exposure dependency exists, conditional logistic regression can be biased. However, this bias has not been well studied. METHODS: We have extended findings by Vines and Farrington to develop a weighting method for the case-crossover study which removes bias from within-subject exposure dependency. Our method calculates the exposure probability at the case period in the case-crossover study which is used to weight the likelihood formulae presented by Greenland in 1999. We simulated data for the population with a disease where most patients receive a cyclic treatment pattern with within-subject exposure dependency but no time trends while some patients stop and start treatment. Finally, the method was applied to real-world data from Japan to study the association between celecoxib and peripheral edema and to study the association between selective serotonin reuptake inhibitor (SSRI) and hip fracture in Australia. RESULTS: When the simulated rate ratio of the outcome was 4.0 in a case-crossover study with no time-varying confounder, the proposed weighting method and the Mantel-Haenszel odds ratio reproduced the true rate ratio. When a time-varying confounder existed, the Mantel-Haenszel method was biased but the weighting method was not. When more than one control period was used, standard conditional logistic regression was biased either with or without time-varying confounding and the bias increased (up to 8.7) when the study period was extended. In real-world analysis with a binary exposure variable in Japan and Australia, the point estimate of the odds ratio (around 2.5 for the association between celecoxib and peripheral edema and around 1.6 between SSRI and hip fracture) by our weighting method was equal to the Mantel-Haenszel odds ratio and stable compared with standard conditional logistic regression. CONCLUSION: Case-crossover studies may be biased from within-subject exposure dependency, even without exposure time trends. This bias can be identified by comparing the odds ratio by the Mantel-Haenszel method and that by standard conditional logistic regression. We recommend using our proposed method which removes bias from within-subject exposure dependency and can account for time-varying confounders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01408-5.
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spelling pubmed-85206202021-10-20 A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies Kubota, Kiyoshi Kelly, Thu-Lan Sato, Tsugumichi Pratt, Nicole Roughead, Elizabeth Yamaguchi, Takuhiro BMC Med Res Methodol Research BACKGROUND: Case-crossover studies have been widely used in various fields including pharmacoepidemiology. Vines and Farrington indicated in 2001 that when within-subject exposure dependency exists, conditional logistic regression can be biased. However, this bias has not been well studied. METHODS: We have extended findings by Vines and Farrington to develop a weighting method for the case-crossover study which removes bias from within-subject exposure dependency. Our method calculates the exposure probability at the case period in the case-crossover study which is used to weight the likelihood formulae presented by Greenland in 1999. We simulated data for the population with a disease where most patients receive a cyclic treatment pattern with within-subject exposure dependency but no time trends while some patients stop and start treatment. Finally, the method was applied to real-world data from Japan to study the association between celecoxib and peripheral edema and to study the association between selective serotonin reuptake inhibitor (SSRI) and hip fracture in Australia. RESULTS: When the simulated rate ratio of the outcome was 4.0 in a case-crossover study with no time-varying confounder, the proposed weighting method and the Mantel-Haenszel odds ratio reproduced the true rate ratio. When a time-varying confounder existed, the Mantel-Haenszel method was biased but the weighting method was not. When more than one control period was used, standard conditional logistic regression was biased either with or without time-varying confounding and the bias increased (up to 8.7) when the study period was extended. In real-world analysis with a binary exposure variable in Japan and Australia, the point estimate of the odds ratio (around 2.5 for the association between celecoxib and peripheral edema and around 1.6 between SSRI and hip fracture) by our weighting method was equal to the Mantel-Haenszel odds ratio and stable compared with standard conditional logistic regression. CONCLUSION: Case-crossover studies may be biased from within-subject exposure dependency, even without exposure time trends. This bias can be identified by comparing the odds ratio by the Mantel-Haenszel method and that by standard conditional logistic regression. We recommend using our proposed method which removes bias from within-subject exposure dependency and can account for time-varying confounders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01408-5. BioMed Central 2021-10-17 /pmc/articles/PMC8520620/ /pubmed/34657592 http://dx.doi.org/10.1186/s12874-021-01408-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kubota, Kiyoshi
Kelly, Thu-Lan
Sato, Tsugumichi
Pratt, Nicole
Roughead, Elizabeth
Yamaguchi, Takuhiro
A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title_full A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title_fullStr A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title_full_unstemmed A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title_short A novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
title_sort novel weighting method to remove bias from within-subject exposure dependency in case-crossover studies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520620/
https://www.ncbi.nlm.nih.gov/pubmed/34657592
http://dx.doi.org/10.1186/s12874-021-01408-5
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