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Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models

Transmission of Ross River virus (RRV) is influenced by climatic, environmental, and socio-economic factors. Accurate and robust predictions based on these factors are necessary for disease prevention and control. However, the complicated transmission cycle and the characteristics of RRV notificatio...

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Autores principales: Qian, Wei, Harley, David, Glass, Kathryn, Viennet, Elvina, Hurst, Cameron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651042/
https://www.ncbi.nlm.nih.gov/pubmed/36389410
http://dx.doi.org/10.7717/peerj.14213
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author Qian, Wei
Harley, David
Glass, Kathryn
Viennet, Elvina
Hurst, Cameron
author_facet Qian, Wei
Harley, David
Glass, Kathryn
Viennet, Elvina
Hurst, Cameron
author_sort Qian, Wei
collection PubMed
description Transmission of Ross River virus (RRV) is influenced by climatic, environmental, and socio-economic factors. Accurate and robust predictions based on these factors are necessary for disease prevention and control. However, the complicated transmission cycle and the characteristics of RRV notification data present challenges. Studies to compare model performance are lacking. In this study, we used RRV notification data and exposure data from 2001 to 2020 in Queensland, Australia, and compared ten models (including generalised linear models, zero-inflated models, and generalised additive models) to predict RRV incidence in different regions of Queensland. We aimed to compare model performance and to evaluate the effect of statistical over-dispersion and zero-inflation of RRV surveillance data, and non-linearity of predictors on model fit. A variable selection strategy for screening important predictors was developed and was found to be efficient and able to generate consistent and reasonable numbers of predictors across regions and in all training sets. Negative binomial models generally exhibited better model fit than Poisson models, suggesting that over-dispersion in the data is the primary factor driving model fit compared to non-linearity of predictors and excess zeros. All models predicted the peak periods well but were unable to fit and predict the magnitude of peaks, especially when there were high numbers of cases. Adding new variables including historical RRV cases and mosquito abundance may improve model performance. The standard negative binomial generalised linear model is stable, simple, and effective in prediction, and is thus considered the best choice among all models.
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spelling pubmed-96510422022-11-15 Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models Qian, Wei Harley, David Glass, Kathryn Viennet, Elvina Hurst, Cameron PeerJ Epidemiology Transmission of Ross River virus (RRV) is influenced by climatic, environmental, and socio-economic factors. Accurate and robust predictions based on these factors are necessary for disease prevention and control. However, the complicated transmission cycle and the characteristics of RRV notification data present challenges. Studies to compare model performance are lacking. In this study, we used RRV notification data and exposure data from 2001 to 2020 in Queensland, Australia, and compared ten models (including generalised linear models, zero-inflated models, and generalised additive models) to predict RRV incidence in different regions of Queensland. We aimed to compare model performance and to evaluate the effect of statistical over-dispersion and zero-inflation of RRV surveillance data, and non-linearity of predictors on model fit. A variable selection strategy for screening important predictors was developed and was found to be efficient and able to generate consistent and reasonable numbers of predictors across regions and in all training sets. Negative binomial models generally exhibited better model fit than Poisson models, suggesting that over-dispersion in the data is the primary factor driving model fit compared to non-linearity of predictors and excess zeros. All models predicted the peak periods well but were unable to fit and predict the magnitude of peaks, especially when there were high numbers of cases. Adding new variables including historical RRV cases and mosquito abundance may improve model performance. The standard negative binomial generalised linear model is stable, simple, and effective in prediction, and is thus considered the best choice among all models. PeerJ Inc. 2022-11-08 /pmc/articles/PMC9651042/ /pubmed/36389410 http://dx.doi.org/10.7717/peerj.14213 Text en ©2022 Qian et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Epidemiology
Qian, Wei
Harley, David
Glass, Kathryn
Viennet, Elvina
Hurst, Cameron
Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title_full Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title_fullStr Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title_full_unstemmed Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title_short Prediction of Ross River virus incidence in Queensland, Australia: building and comparing models
title_sort prediction of ross river virus incidence in queensland, australia: building and comparing models
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651042/
https://www.ncbi.nlm.nih.gov/pubmed/36389410
http://dx.doi.org/10.7717/peerj.14213
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