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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
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.
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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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