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Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach

BACKGROUND: An important public health goal is to decrease the prevalence of key behavioural risk factors, such as tobacco use and obesity. Survey information is often available at the regional level, but heterogeneity within large geographic regions cannot be assessed. Advanced spatial analysis tec...

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Autores principales: Seliske, L., Norwood, T. A., McLaughlin, J. R., Wang, S., Palleschi, C., Holowaty, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897930/
https://www.ncbi.nlm.nih.gov/pubmed/27266873
http://dx.doi.org/10.1186/s12889-016-3144-4
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author Seliske, L.
Norwood, T. A.
McLaughlin, J. R.
Wang, S.
Palleschi, C.
Holowaty, E.
author_facet Seliske, L.
Norwood, T. A.
McLaughlin, J. R.
Wang, S.
Palleschi, C.
Holowaty, E.
author_sort Seliske, L.
collection PubMed
description BACKGROUND: An important public health goal is to decrease the prevalence of key behavioural risk factors, such as tobacco use and obesity. Survey information is often available at the regional level, but heterogeneity within large geographic regions cannot be assessed. Advanced spatial analysis techniques are demonstrated to produce sensible micro area estimates of behavioural risk factors that enable identification of areas with high prevalence. METHODS: A spatial Bayesian hierarchical model was used to estimate the micro area prevalence of current smoking and excess bodyweight for the Erie-St. Clair region in southwestern Ontario. Estimates were mapped for male and female respondents of five cycles of the Canadian Community Health Survey (CCHS). The micro areas were 2006 Census Dissemination Areas, with an average population of 400–700 people. Two individual-level models were specified: one controlled for survey cycle and age group (model 1), and one controlled for survey cycle, age group and micro area median household income (model 2). Post-stratification was used to derive micro area behavioural risk factor estimates weighted to the population structure. SaTScan analyses were conducted on the granular, postal-code level CCHS data to corroborate findings of elevated prevalence. RESULTS: Current smoking was elevated in two urban areas for both sexes (Sarnia and Windsor), and an additional small community (Chatham) for males only. Areas of excess bodyweight were prevalent in an urban core (Windsor) among males, but not females. Precision of the posterior post-stratified current smoking estimates was improved in model 2, as indicated by narrower credible intervals and a lower coefficient of variation. For excess bodyweight, both models had similar precision. Aggregation of the micro area estimates to CCHS design-based estimates validated the findings. CONCLUSIONS: This is among the first studies to apply a full Bayesian model to complex sample survey data to identify micro areas with variation in risk factor prevalence, accounting for spatial correlation and other covariates. Application of micro area analysis techniques helps define areas for public health planning, and may be informative to surveillance and research modeling of relevant chronic disease outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-016-3144-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-48979302016-06-09 Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach Seliske, L. Norwood, T. A. McLaughlin, J. R. Wang, S. Palleschi, C. Holowaty, E. BMC Public Health Research Article BACKGROUND: An important public health goal is to decrease the prevalence of key behavioural risk factors, such as tobacco use and obesity. Survey information is often available at the regional level, but heterogeneity within large geographic regions cannot be assessed. Advanced spatial analysis techniques are demonstrated to produce sensible micro area estimates of behavioural risk factors that enable identification of areas with high prevalence. METHODS: A spatial Bayesian hierarchical model was used to estimate the micro area prevalence of current smoking and excess bodyweight for the Erie-St. Clair region in southwestern Ontario. Estimates were mapped for male and female respondents of five cycles of the Canadian Community Health Survey (CCHS). The micro areas were 2006 Census Dissemination Areas, with an average population of 400–700 people. Two individual-level models were specified: one controlled for survey cycle and age group (model 1), and one controlled for survey cycle, age group and micro area median household income (model 2). Post-stratification was used to derive micro area behavioural risk factor estimates weighted to the population structure. SaTScan analyses were conducted on the granular, postal-code level CCHS data to corroborate findings of elevated prevalence. RESULTS: Current smoking was elevated in two urban areas for both sexes (Sarnia and Windsor), and an additional small community (Chatham) for males only. Areas of excess bodyweight were prevalent in an urban core (Windsor) among males, but not females. Precision of the posterior post-stratified current smoking estimates was improved in model 2, as indicated by narrower credible intervals and a lower coefficient of variation. For excess bodyweight, both models had similar precision. Aggregation of the micro area estimates to CCHS design-based estimates validated the findings. CONCLUSIONS: This is among the first studies to apply a full Bayesian model to complex sample survey data to identify micro areas with variation in risk factor prevalence, accounting for spatial correlation and other covariates. Application of micro area analysis techniques helps define areas for public health planning, and may be informative to surveillance and research modeling of relevant chronic disease outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-016-3144-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-07 /pmc/articles/PMC4897930/ /pubmed/27266873 http://dx.doi.org/10.1186/s12889-016-3144-4 Text en © Seliske 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
Seliske, L.
Norwood, T. A.
McLaughlin, J. R.
Wang, S.
Palleschi, C.
Holowaty, E.
Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title_full Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title_fullStr Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title_full_unstemmed Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title_short Estimating micro area behavioural risk factor prevalence from large population-based surveys: a full Bayesian approach
title_sort estimating micro area behavioural risk factor prevalence from large population-based surveys: a full bayesian approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897930/
https://www.ncbi.nlm.nih.gov/pubmed/27266873
http://dx.doi.org/10.1186/s12889-016-3144-4
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