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Quantitative methods for descriptive intersectional analysis with binary health outcomes

Intersectionality recognizes that in the context of sociohistorically shaped structural power relations, an individual's multiple social positions or identities (e.g., gender, ethnicity) can interact to affect health-related outcomes. Despite limited methodological guidance, intersectionality f...

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Detalles Bibliográficos
Autores principales: Mahendran, Mayuri, Lizotte, Daniel, Bauer, Greta R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800141/
https://www.ncbi.nlm.nih.gov/pubmed/35118188
http://dx.doi.org/10.1016/j.ssmph.2022.101032
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author Mahendran, Mayuri
Lizotte, Daniel
Bauer, Greta R.
author_facet Mahendran, Mayuri
Lizotte, Daniel
Bauer, Greta R.
author_sort Mahendran, Mayuri
collection PubMed
description Intersectionality recognizes that in the context of sociohistorically shaped structural power relations, an individual's multiple social positions or identities (e.g., gender, ethnicity) can interact to affect health-related outcomes. Despite limited methodological guidance, intersectionality frameworks have increasingly been incorporated into epidemiological studies, both to describe health disparities and to examine their causes. This study aimed to advance methods in intersectional estimation of binary outcomes in descriptive health disparities research through evaluation of 7 potentially intersectional data analysis methods: cross-classification, regression with interactions, multilevel analysis of individual heterogeneity (MAIHDA), and decision trees (CART, CTree, CHAID, random forest). Accuracy of estimated intersection-specific outcome prevalence was evaluated across 192 intersections using simulated data scenarios. For comparison we included a non-intersectional main effects regression. We additionally assessed variable selection performance amongst decision trees. Example analyses using National Health and Nutrition Examination Study data illustrated differences in results between methods. At larger sample sizes, all methods except for CART performed better than non-intersectional main effects regression. In smaller samples, MAIHDA was the most accurate method but showed no advantage over main effects regression, while random forest, cross-classification, and saturated regression were the least accurate, and CTree and CHAID performed moderately well. CART performed poorly for estimation and variable selection. Sensitivity analyses examining the bias-variance tradeoff suggest MAIHDA as the preferred unbiased method for accurate estimation of high-dimensional intersections at smaller sample sizes. Larger sample sizes are more imperative for other methods. Results support the adoption of an intersectional approach to descriptive epidemiology.
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spelling pubmed-88001412022-02-02 Quantitative methods for descriptive intersectional analysis with binary health outcomes Mahendran, Mayuri Lizotte, Daniel Bauer, Greta R. SSM Popul Health Article Intersectionality recognizes that in the context of sociohistorically shaped structural power relations, an individual's multiple social positions or identities (e.g., gender, ethnicity) can interact to affect health-related outcomes. Despite limited methodological guidance, intersectionality frameworks have increasingly been incorporated into epidemiological studies, both to describe health disparities and to examine their causes. This study aimed to advance methods in intersectional estimation of binary outcomes in descriptive health disparities research through evaluation of 7 potentially intersectional data analysis methods: cross-classification, regression with interactions, multilevel analysis of individual heterogeneity (MAIHDA), and decision trees (CART, CTree, CHAID, random forest). Accuracy of estimated intersection-specific outcome prevalence was evaluated across 192 intersections using simulated data scenarios. For comparison we included a non-intersectional main effects regression. We additionally assessed variable selection performance amongst decision trees. Example analyses using National Health and Nutrition Examination Study data illustrated differences in results between methods. At larger sample sizes, all methods except for CART performed better than non-intersectional main effects regression. In smaller samples, MAIHDA was the most accurate method but showed no advantage over main effects regression, while random forest, cross-classification, and saturated regression were the least accurate, and CTree and CHAID performed moderately well. CART performed poorly for estimation and variable selection. Sensitivity analyses examining the bias-variance tradeoff suggest MAIHDA as the preferred unbiased method for accurate estimation of high-dimensional intersections at smaller sample sizes. Larger sample sizes are more imperative for other methods. Results support the adoption of an intersectional approach to descriptive epidemiology. Elsevier 2022-01-22 /pmc/articles/PMC8800141/ /pubmed/35118188 http://dx.doi.org/10.1016/j.ssmph.2022.101032 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mahendran, Mayuri
Lizotte, Daniel
Bauer, Greta R.
Quantitative methods for descriptive intersectional analysis with binary health outcomes
title Quantitative methods for descriptive intersectional analysis with binary health outcomes
title_full Quantitative methods for descriptive intersectional analysis with binary health outcomes
title_fullStr Quantitative methods for descriptive intersectional analysis with binary health outcomes
title_full_unstemmed Quantitative methods for descriptive intersectional analysis with binary health outcomes
title_short Quantitative methods for descriptive intersectional analysis with binary health outcomes
title_sort quantitative methods for descriptive intersectional analysis with binary health outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800141/
https://www.ncbi.nlm.nih.gov/pubmed/35118188
http://dx.doi.org/10.1016/j.ssmph.2022.101032
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