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Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria

BACKGROUND: Gametocytes are the sexual form of the malaria parasite and the main agents of transmission. While there are several factors that influence host infectivity, the density of gametocytes appears to be the best single measure that is related to the human host's infectivity to mosquitoe...

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Autores principales: Distiller, Greg B, Little, Francesca, Barnes, Karen I
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845183/
https://www.ncbi.nlm.nih.gov/pubmed/20187935
http://dx.doi.org/10.1186/1475-2875-9-60
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author Distiller, Greg B
Little, Francesca
Barnes, Karen I
author_facet Distiller, Greg B
Little, Francesca
Barnes, Karen I
author_sort Distiller, Greg B
collection PubMed
description BACKGROUND: Gametocytes are the sexual form of the malaria parasite and the main agents of transmission. While there are several factors that influence host infectivity, the density of gametocytes appears to be the best single measure that is related to the human host's infectivity to mosquitoes. Despite the obviously important role that gametocytes play in the transmission of malaria and spread of anti-malarial resistance, it is common to estimate gametocyte carriage indirectly based on asexual parasite measurements. The objective of this research was to directly model observed gametocyte densities over time, during the primary infection. METHODS: Of 447 patients enrolled in sulphadoxine-pyrimethamine therapeutic efficacy studies in South Africa and Mozambique, a subset of 103 patients who had no gametocytes pre-treatment and who had at least three non-zero gametocyte densities over the 42-day follow up period were included in this analysis. RESULTS: A variety of different functions were examined. A modified version of the critical exponential function was selected for the final model given its robustness across different datasets and its flexibility in assuming a variety of different shapes. Age, site, initial asexual parasite density (logged to the base 10), and an empirical patient category were the co-variates that were found to improve the model. CONCLUSIONS: A population nonlinear modeling approach seems promising and produced a flexible function whose estimates were stable across various different datasets. Surprisingly, dihydrofolate reductase and dihydropteroate synthetase mutation prevalence did not enter the model. This is probably related to a lack of power (quintuple mutations n = 12), and informative censoring; treatment failures were withdrawn from the study and given rescue treatment, usually prior to completion of follow up.
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spelling pubmed-28451832010-03-26 Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria Distiller, Greg B Little, Francesca Barnes, Karen I Malar J Research BACKGROUND: Gametocytes are the sexual form of the malaria parasite and the main agents of transmission. While there are several factors that influence host infectivity, the density of gametocytes appears to be the best single measure that is related to the human host's infectivity to mosquitoes. Despite the obviously important role that gametocytes play in the transmission of malaria and spread of anti-malarial resistance, it is common to estimate gametocyte carriage indirectly based on asexual parasite measurements. The objective of this research was to directly model observed gametocyte densities over time, during the primary infection. METHODS: Of 447 patients enrolled in sulphadoxine-pyrimethamine therapeutic efficacy studies in South Africa and Mozambique, a subset of 103 patients who had no gametocytes pre-treatment and who had at least three non-zero gametocyte densities over the 42-day follow up period were included in this analysis. RESULTS: A variety of different functions were examined. A modified version of the critical exponential function was selected for the final model given its robustness across different datasets and its flexibility in assuming a variety of different shapes. Age, site, initial asexual parasite density (logged to the base 10), and an empirical patient category were the co-variates that were found to improve the model. CONCLUSIONS: A population nonlinear modeling approach seems promising and produced a flexible function whose estimates were stable across various different datasets. Surprisingly, dihydrofolate reductase and dihydropteroate synthetase mutation prevalence did not enter the model. This is probably related to a lack of power (quintuple mutations n = 12), and informative censoring; treatment failures were withdrawn from the study and given rescue treatment, usually prior to completion of follow up. BioMed Central 2010-02-26 /pmc/articles/PMC2845183/ /pubmed/20187935 http://dx.doi.org/10.1186/1475-2875-9-60 Text en Copyright ©2010 Distiller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Distiller, Greg B
Little, Francesca
Barnes, Karen I
Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title_full Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title_fullStr Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title_full_unstemmed Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title_short Nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
title_sort nonlinear mixed effects modeling of gametocyte carriage in patients with uncomplicated malaria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845183/
https://www.ncbi.nlm.nih.gov/pubmed/20187935
http://dx.doi.org/10.1186/1475-2875-9-60
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