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Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia

Overdispersed count data arise commonly in disease mapping and infectious disease studies. Typically, the level of overdispersion is assumed to be constant over time and space. In some applications, however, this assumption is violated, and in such cases, it is necessary to model the dispersion as a...

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Autores principales: Mutiso, Fedelis, Pearce, John L., Benjamin-Neelon, Sara E., Mueller, Noel T., Li, Hong, Neelon, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500097/
https://www.ncbi.nlm.nih.gov/pubmed/36168515
http://dx.doi.org/10.1016/j.spasta.2022.100703
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author Mutiso, Fedelis
Pearce, John L.
Benjamin-Neelon, Sara E.
Mueller, Noel T.
Li, Hong
Neelon, Brian
author_facet Mutiso, Fedelis
Pearce, John L.
Benjamin-Neelon, Sara E.
Mueller, Noel T.
Li, Hong
Neelon, Brian
author_sort Mutiso, Fedelis
collection PubMed
description Overdispersed count data arise commonly in disease mapping and infectious disease studies. Typically, the level of overdispersion is assumed to be constant over time and space. In some applications, however, this assumption is violated, and in such cases, it is necessary to model the dispersion as a function of time and space in order to obtain valid inferences. Motivated by a study examining spatiotemporal patterns in COVID-19 incidence, we develop a Bayesian negative binomial model that accounts for heterogeneity in both the incidence rate and degree of overdispersion. To fully capture the heterogeneity in the data, we introduce region-level covariates, smooth temporal effects, and spatially correlated random effects in both the mean and dispersion components of the model. The random effects are assigned bivariate intrinsic conditionally autoregressive priors that promote spatial smoothing and permit the model components to borrow information, which is appealing when the mean and dispersion are spatially correlated. Through simulation studies, we show that ignoring heterogeneity in the dispersion can lead to biased and imprecise estimates. For estimation, we adopt a Bayesian approach that combines full-conditional Gibbs sampling and Metropolis–Hastings steps. We apply the model to a study of COVID-19 incidence in the state of Georgia, USA from March 15 to December 31, 2020.
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spelling pubmed-95000972022-09-23 Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia Mutiso, Fedelis Pearce, John L. Benjamin-Neelon, Sara E. Mueller, Noel T. Li, Hong Neelon, Brian Spat Stat Article Overdispersed count data arise commonly in disease mapping and infectious disease studies. Typically, the level of overdispersion is assumed to be constant over time and space. In some applications, however, this assumption is violated, and in such cases, it is necessary to model the dispersion as a function of time and space in order to obtain valid inferences. Motivated by a study examining spatiotemporal patterns in COVID-19 incidence, we develop a Bayesian negative binomial model that accounts for heterogeneity in both the incidence rate and degree of overdispersion. To fully capture the heterogeneity in the data, we introduce region-level covariates, smooth temporal effects, and spatially correlated random effects in both the mean and dispersion components of the model. The random effects are assigned bivariate intrinsic conditionally autoregressive priors that promote spatial smoothing and permit the model components to borrow information, which is appealing when the mean and dispersion are spatially correlated. Through simulation studies, we show that ignoring heterogeneity in the dispersion can lead to biased and imprecise estimates. For estimation, we adopt a Bayesian approach that combines full-conditional Gibbs sampling and Metropolis–Hastings steps. We apply the model to a study of COVID-19 incidence in the state of Georgia, USA from March 15 to December 31, 2020. Elsevier B.V. 2022-12 2022-09-23 /pmc/articles/PMC9500097/ /pubmed/36168515 http://dx.doi.org/10.1016/j.spasta.2022.100703 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Mutiso, Fedelis
Pearce, John L.
Benjamin-Neelon, Sara E.
Mueller, Noel T.
Li, Hong
Neelon, Brian
Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title_full Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title_fullStr Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title_full_unstemmed Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title_short Bayesian negative binomial regression with spatially varying dispersion: Modeling COVID-19 incidence in Georgia
title_sort bayesian negative binomial regression with spatially varying dispersion: modeling covid-19 incidence in georgia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500097/
https://www.ncbi.nlm.nih.gov/pubmed/36168515
http://dx.doi.org/10.1016/j.spasta.2022.100703
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