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Evaluating the impact of a small number of areas on spatial estimation

BACKGROUND: There is an expanding literature on different representations of spatial random effects for different types of spatial correlation structure within the conditional autoregressive class of priors for Bayesian spatial models. However, little is known about the impact of these different pri...

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Autores principales: Aswi, Aswi, Cramb, Susanna, Duncan, Earl, Mengersen, Kerrie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519538/
https://www.ncbi.nlm.nih.gov/pubmed/32977803
http://dx.doi.org/10.1186/s12942-020-00233-1
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author Aswi, Aswi
Cramb, Susanna
Duncan, Earl
Mengersen, Kerrie
author_facet Aswi, Aswi
Cramb, Susanna
Duncan, Earl
Mengersen, Kerrie
author_sort Aswi, Aswi
collection PubMed
description BACKGROUND: There is an expanding literature on different representations of spatial random effects for different types of spatial correlation structure within the conditional autoregressive class of priors for Bayesian spatial models. However, little is known about the impact of these different priors when the number of areas is small. This paper aimed to investigate this problem both in the context of a case study of spatial analysis of dengue fever and more generally through a simulation study. METHODS: Both the simulation study and the case study considered count data aggregated to a small area level in a region. Five different conditional autoregressive priors for a simple Bayesian Poisson model were considered: independent, Besag-York-Mollié, Leroux, and two variants of a localised clustering model. Data were simulated with eight different sizes of areal grids, ranging from 4 to 2500 areas, and two different levels of both spatial autocorrelation and disease counts. Model goodness-of-fit measures and model estimates were compared. A case study involving dengue fever cases in 14 local areas in Makassar, Indonesia, was also considered. RESULTS: The simulation study showed that model performance varied under different scenarios. When areas had low autocorrelation and high counts, and the number of areas was at most 25, the BYM, Leroux and localised [Formula: see text] models performed similarly and better than the independent and localised [Formula: see text] models. However, when the number of areas were at least 100, all models performed differently, and the Leroux model performed the best. Overall, the Leroux model performed the best for every scenario especially when there were at least 16 areas. Based on the case study, the comparative performance of spatial models may also vary for a small number of areas, especially when the data have a relatively large mean and variance over areas. In this case, the localised model with G = 3 was a better choice. CONCLUSION: Detecting spatial patterns can be difficult when there are very few areas. Understanding the characteristics of the data and the relative influence of alternative conditional autoregressive priors is essential in selecting an appropriate Bayesian spatial model.
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spelling pubmed-75195382020-09-29 Evaluating the impact of a small number of areas on spatial estimation Aswi, Aswi Cramb, Susanna Duncan, Earl Mengersen, Kerrie Int J Health Geogr Research BACKGROUND: There is an expanding literature on different representations of spatial random effects for different types of spatial correlation structure within the conditional autoregressive class of priors for Bayesian spatial models. However, little is known about the impact of these different priors when the number of areas is small. This paper aimed to investigate this problem both in the context of a case study of spatial analysis of dengue fever and more generally through a simulation study. METHODS: Both the simulation study and the case study considered count data aggregated to a small area level in a region. Five different conditional autoregressive priors for a simple Bayesian Poisson model were considered: independent, Besag-York-Mollié, Leroux, and two variants of a localised clustering model. Data were simulated with eight different sizes of areal grids, ranging from 4 to 2500 areas, and two different levels of both spatial autocorrelation and disease counts. Model goodness-of-fit measures and model estimates were compared. A case study involving dengue fever cases in 14 local areas in Makassar, Indonesia, was also considered. RESULTS: The simulation study showed that model performance varied under different scenarios. When areas had low autocorrelation and high counts, and the number of areas was at most 25, the BYM, Leroux and localised [Formula: see text] models performed similarly and better than the independent and localised [Formula: see text] models. However, when the number of areas were at least 100, all models performed differently, and the Leroux model performed the best. Overall, the Leroux model performed the best for every scenario especially when there were at least 16 areas. Based on the case study, the comparative performance of spatial models may also vary for a small number of areas, especially when the data have a relatively large mean and variance over areas. In this case, the localised model with G = 3 was a better choice. CONCLUSION: Detecting spatial patterns can be difficult when there are very few areas. Understanding the characteristics of the data and the relative influence of alternative conditional autoregressive priors is essential in selecting an appropriate Bayesian spatial model. BioMed Central 2020-09-25 /pmc/articles/PMC7519538/ /pubmed/32977803 http://dx.doi.org/10.1186/s12942-020-00233-1 Text en © The Author(s) 2020 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/. 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 in a credit line to the data.
spellingShingle Research
Aswi, Aswi
Cramb, Susanna
Duncan, Earl
Mengersen, Kerrie
Evaluating the impact of a small number of areas on spatial estimation
title Evaluating the impact of a small number of areas on spatial estimation
title_full Evaluating the impact of a small number of areas on spatial estimation
title_fullStr Evaluating the impact of a small number of areas on spatial estimation
title_full_unstemmed Evaluating the impact of a small number of areas on spatial estimation
title_short Evaluating the impact of a small number of areas on spatial estimation
title_sort evaluating the impact of a small number of areas on spatial estimation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519538/
https://www.ncbi.nlm.nih.gov/pubmed/32977803
http://dx.doi.org/10.1186/s12942-020-00233-1
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