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Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria
In many countries health system data remain too weak to accurately enumerate Plasmodium falciparum malaria cases. In response, cartographic approaches have been developed that link maps of infection prevalence with mathematical relationships to predict the incidence rate of clinical malaria. Microsi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569718/ https://www.ncbi.nlm.nih.gov/pubmed/26348689 http://dx.doi.org/10.1038/ncomms9170 |
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author | Cameron, Ewan Battle, Katherine E. Bhatt, Samir Weiss, Daniel J. Bisanzio, Donal Mappin, Bonnie Dalrymple, Ursula Hay, Simon I. Smith, David L. Griffin, Jamie T. Wenger, Edward A. Eckhoff, Philip A. Smith, Thomas A. Penny, Melissa A. Gething, Peter W. |
author_facet | Cameron, Ewan Battle, Katherine E. Bhatt, Samir Weiss, Daniel J. Bisanzio, Donal Mappin, Bonnie Dalrymple, Ursula Hay, Simon I. Smith, David L. Griffin, Jamie T. Wenger, Edward A. Eckhoff, Philip A. Smith, Thomas A. Penny, Melissa A. Gething, Peter W. |
author_sort | Cameron, Ewan |
collection | PubMed |
description | In many countries health system data remain too weak to accurately enumerate Plasmodium falciparum malaria cases. In response, cartographic approaches have been developed that link maps of infection prevalence with mathematical relationships to predict the incidence rate of clinical malaria. Microsimulation (or ‘agent-based') models represent a powerful new paradigm for defining such relationships; however, differences in model structure and calibration data mean that no consensus yet exists on the optimal form for use in disease-burden estimation. Here we develop a Bayesian statistical procedure combining functional regression-based model emulation with Markov Chain Monte Carlo sampling to calibrate three selected microsimulation models against a purpose-built data set of age-structured prevalence and incidence counts. This allows the generation of ensemble forecasts of the prevalence–incidence relationship stratified by age, transmission seasonality, treatment level and exposure history, from which we predict accelerating returns on investments in large-scale intervention campaigns as transmission and prevalence are progressively reduced. |
format | Online Article Text |
id | pubmed-4569718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45697182015-09-28 Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria Cameron, Ewan Battle, Katherine E. Bhatt, Samir Weiss, Daniel J. Bisanzio, Donal Mappin, Bonnie Dalrymple, Ursula Hay, Simon I. Smith, David L. Griffin, Jamie T. Wenger, Edward A. Eckhoff, Philip A. Smith, Thomas A. Penny, Melissa A. Gething, Peter W. Nat Commun Article In many countries health system data remain too weak to accurately enumerate Plasmodium falciparum malaria cases. In response, cartographic approaches have been developed that link maps of infection prevalence with mathematical relationships to predict the incidence rate of clinical malaria. Microsimulation (or ‘agent-based') models represent a powerful new paradigm for defining such relationships; however, differences in model structure and calibration data mean that no consensus yet exists on the optimal form for use in disease-burden estimation. Here we develop a Bayesian statistical procedure combining functional regression-based model emulation with Markov Chain Monte Carlo sampling to calibrate three selected microsimulation models against a purpose-built data set of age-structured prevalence and incidence counts. This allows the generation of ensemble forecasts of the prevalence–incidence relationship stratified by age, transmission seasonality, treatment level and exposure history, from which we predict accelerating returns on investments in large-scale intervention campaigns as transmission and prevalence are progressively reduced. Nature Pub. Group 2015-09-08 /pmc/articles/PMC4569718/ /pubmed/26348689 http://dx.doi.org/10.1038/ncomms9170 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cameron, Ewan Battle, Katherine E. Bhatt, Samir Weiss, Daniel J. Bisanzio, Donal Mappin, Bonnie Dalrymple, Ursula Hay, Simon I. Smith, David L. Griffin, Jamie T. Wenger, Edward A. Eckhoff, Philip A. Smith, Thomas A. Penny, Melissa A. Gething, Peter W. Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title | Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title_full | Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title_fullStr | Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title_full_unstemmed | Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title_short | Defining the relationship between infection prevalence and clinical incidence of Plasmodium falciparum malaria |
title_sort | defining the relationship between infection prevalence and clinical incidence of plasmodium falciparum malaria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569718/ https://www.ncbi.nlm.nih.gov/pubmed/26348689 http://dx.doi.org/10.1038/ncomms9170 |
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