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Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models

BACKGROUND: The distribution of Plasmodium falciparum clinical malaria episodes is over-dispersed among children in endemic areas, with more children experiencing multiple clinical episodes than would be expected based on a Poisson distribution. There is consistent evidence for micro-epidemiological...

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Autores principales: Ndungu, Francis Maina, Marsh, Kevin, Fegan, Gregory, Wambua, Juliana, Nyangweso, George, Ogada, Edna, Mwangi, Tabitha, Nyundo, Chris, Macharia, Alex, Uyoga, Sophie, Williams, Thomas N, Bejon, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527301/
https://www.ncbi.nlm.nih.gov/pubmed/26248615
http://dx.doi.org/10.1186/s12916-015-0422-4
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author Ndungu, Francis Maina
Marsh, Kevin
Fegan, Gregory
Wambua, Juliana
Nyangweso, George
Ogada, Edna
Mwangi, Tabitha
Nyundo, Chris
Macharia, Alex
Uyoga, Sophie
Williams, Thomas N
Bejon, Philip
author_facet Ndungu, Francis Maina
Marsh, Kevin
Fegan, Gregory
Wambua, Juliana
Nyangweso, George
Ogada, Edna
Mwangi, Tabitha
Nyundo, Chris
Macharia, Alex
Uyoga, Sophie
Williams, Thomas N
Bejon, Philip
author_sort Ndungu, Francis Maina
collection PubMed
description BACKGROUND: The distribution of Plasmodium falciparum clinical malaria episodes is over-dispersed among children in endemic areas, with more children experiencing multiple clinical episodes than would be expected based on a Poisson distribution. There is consistent evidence for micro-epidemiological variation in exposure to P. falciparum. The aim of the current study was to identify children with excess malaria episodes after controlling for malaria exposure. METHODS: We selected the model that best fit the data out of the models examined and included the following covariates: age, a weighted local prevalence of infection as an index of exposure, and calendar time to predict episodes of malaria on active surveillance malaria data from 2,463 children of under 15 years of age followed for between 5 and 15 years each. Using parameters from the zero-inflated negative binomial model which best fitted our data, we ran 100 simulations of the model based on our population to determine the variation that might be seen due to chance. RESULTS: We identified 212 out of 2,463 children who had a number of clinical episodes above the 95(th) percentile of the simulations run from the model, hereafter referred to as “excess malaria (EM)”. We then identified exposure-matched controls with “average numbers of malaria” episodes, and found that the EM group had higher parasite densities when asymptomatically infected or during clinical malaria, and were less likely to be of haemoglobin AS genotype. CONCLUSIONS: Of the models tested, the negative zero-inflated negative binomial distribution with exposure, calendar year, and age acting as independent predictors, fitted the distribution of clinical malaria the best. Despite accounting for these factors, a group of children suffer excess malaria episodes beyond those predicted by the model. An epidemiological framework for identifying these children will allow us to study factors that may explain excess malaria episodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-015-0422-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-45273012015-08-07 Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models Ndungu, Francis Maina Marsh, Kevin Fegan, Gregory Wambua, Juliana Nyangweso, George Ogada, Edna Mwangi, Tabitha Nyundo, Chris Macharia, Alex Uyoga, Sophie Williams, Thomas N Bejon, Philip BMC Med Research Article BACKGROUND: The distribution of Plasmodium falciparum clinical malaria episodes is over-dispersed among children in endemic areas, with more children experiencing multiple clinical episodes than would be expected based on a Poisson distribution. There is consistent evidence for micro-epidemiological variation in exposure to P. falciparum. The aim of the current study was to identify children with excess malaria episodes after controlling for malaria exposure. METHODS: We selected the model that best fit the data out of the models examined and included the following covariates: age, a weighted local prevalence of infection as an index of exposure, and calendar time to predict episodes of malaria on active surveillance malaria data from 2,463 children of under 15 years of age followed for between 5 and 15 years each. Using parameters from the zero-inflated negative binomial model which best fitted our data, we ran 100 simulations of the model based on our population to determine the variation that might be seen due to chance. RESULTS: We identified 212 out of 2,463 children who had a number of clinical episodes above the 95(th) percentile of the simulations run from the model, hereafter referred to as “excess malaria (EM)”. We then identified exposure-matched controls with “average numbers of malaria” episodes, and found that the EM group had higher parasite densities when asymptomatically infected or during clinical malaria, and were less likely to be of haemoglobin AS genotype. CONCLUSIONS: Of the models tested, the negative zero-inflated negative binomial distribution with exposure, calendar year, and age acting as independent predictors, fitted the distribution of clinical malaria the best. Despite accounting for these factors, a group of children suffer excess malaria episodes beyond those predicted by the model. An epidemiological framework for identifying these children will allow us to study factors that may explain excess malaria episodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-015-0422-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-06 /pmc/articles/PMC4527301/ /pubmed/26248615 http://dx.doi.org/10.1186/s12916-015-0422-4 Text en © Ndungu et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Ndungu, Francis Maina
Marsh, Kevin
Fegan, Gregory
Wambua, Juliana
Nyangweso, George
Ogada, Edna
Mwangi, Tabitha
Nyundo, Chris
Macharia, Alex
Uyoga, Sophie
Williams, Thomas N
Bejon, Philip
Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title_full Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title_fullStr Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title_full_unstemmed Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title_short Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
title_sort identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527301/
https://www.ncbi.nlm.nih.gov/pubmed/26248615
http://dx.doi.org/10.1186/s12916-015-0422-4
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