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Method for mapping population-based case-control studies: an application using generalized additive models

BACKGROUND: Mapping spatial distributions of disease occurrence and risk can serve as a useful tool for identifying exposures of public health concern. Disease registry data are often mapped by town or county of diagnosis and contain limited data on covariates. These maps often possess poor spatial...

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Autores principales: Webster, Thomas, Vieira, Verónica, Weinberg, Janice, Aschengrau, Ann
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526437/
https://www.ncbi.nlm.nih.gov/pubmed/16764727
http://dx.doi.org/10.1186/1476-072X-5-26
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author Webster, Thomas
Vieira, Verónica
Weinberg, Janice
Aschengrau, Ann
author_facet Webster, Thomas
Vieira, Verónica
Weinberg, Janice
Aschengrau, Ann
author_sort Webster, Thomas
collection PubMed
description BACKGROUND: Mapping spatial distributions of disease occurrence and risk can serve as a useful tool for identifying exposures of public health concern. Disease registry data are often mapped by town or county of diagnosis and contain limited data on covariates. These maps often possess poor spatial resolution, the potential for spatial confounding, and the inability to consider latency. Population-based case-control studies can provide detailed information on residential history and covariates. RESULTS: Generalized additive models (GAMs) provide a useful framework for mapping point-based epidemiologic data. Smoothing on location while controlling for covariates produces adjusted maps. We generate maps of odds ratios using the entire study area as a reference. We smooth using a locally weighted regression smoother (loess), a method that combines the advantages of nearest neighbor and kernel methods. We choose an optimal degree of smoothing by minimizing Akaike's Information Criterion. We use a deviance-based test to assess the overall importance of location in the model and pointwise permutation tests to locate regions of significantly increased or decreased risk. The method is illustrated with synthetic data and data from a population-based case-control study, using S-Plus and ArcView software. CONCLUSION: Our goal is to develop practical methods for mapping population-based case-control and cohort studies. The method described here performs well for our synthetic data, reproducing important features of the data and adequately controlling the covariate. When applied to the population-based case-control data set, the method suggests spatial confounding and identifies statistically significant areas of increased and decreased odds ratios.
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spelling pubmed-15264372006-08-03 Method for mapping population-based case-control studies: an application using generalized additive models Webster, Thomas Vieira, Verónica Weinberg, Janice Aschengrau, Ann Int J Health Geogr Research BACKGROUND: Mapping spatial distributions of disease occurrence and risk can serve as a useful tool for identifying exposures of public health concern. Disease registry data are often mapped by town or county of diagnosis and contain limited data on covariates. These maps often possess poor spatial resolution, the potential for spatial confounding, and the inability to consider latency. Population-based case-control studies can provide detailed information on residential history and covariates. RESULTS: Generalized additive models (GAMs) provide a useful framework for mapping point-based epidemiologic data. Smoothing on location while controlling for covariates produces adjusted maps. We generate maps of odds ratios using the entire study area as a reference. We smooth using a locally weighted regression smoother (loess), a method that combines the advantages of nearest neighbor and kernel methods. We choose an optimal degree of smoothing by minimizing Akaike's Information Criterion. We use a deviance-based test to assess the overall importance of location in the model and pointwise permutation tests to locate regions of significantly increased or decreased risk. The method is illustrated with synthetic data and data from a population-based case-control study, using S-Plus and ArcView software. CONCLUSION: Our goal is to develop practical methods for mapping population-based case-control and cohort studies. The method described here performs well for our synthetic data, reproducing important features of the data and adequately controlling the covariate. When applied to the population-based case-control data set, the method suggests spatial confounding and identifies statistically significant areas of increased and decreased odds ratios. BioMed Central 2006-06-09 /pmc/articles/PMC1526437/ /pubmed/16764727 http://dx.doi.org/10.1186/1476-072X-5-26 Text en Copyright © 2006 Webster et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Webster, Thomas
Vieira, Verónica
Weinberg, Janice
Aschengrau, Ann
Method for mapping population-based case-control studies: an application using generalized additive models
title Method for mapping population-based case-control studies: an application using generalized additive models
title_full Method for mapping population-based case-control studies: an application using generalized additive models
title_fullStr Method for mapping population-based case-control studies: an application using generalized additive models
title_full_unstemmed Method for mapping population-based case-control studies: an application using generalized additive models
title_short Method for mapping population-based case-control studies: an application using generalized additive models
title_sort method for mapping population-based case-control studies: an application using generalized additive models
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526437/
https://www.ncbi.nlm.nih.gov/pubmed/16764727
http://dx.doi.org/10.1186/1476-072X-5-26
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