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Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models

BACKGROUND: Serological data are increasingly being used to monitor malaria transmission intensity and have been demonstrated to be particularly useful in areas of low transmission where traditional measures such as EIR and parasite prevalence are limited. The seroconversion rate (SCR) is usually es...

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Autores principales: Pothin, Emilie, Ferguson, Neil M., Drakeley, Chris J., Ghani, Azra C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748547/
https://www.ncbi.nlm.nih.gov/pubmed/26861862
http://dx.doi.org/10.1186/s12936-016-1121-0
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author Pothin, Emilie
Ferguson, Neil M.
Drakeley, Chris J.
Ghani, Azra C.
author_facet Pothin, Emilie
Ferguson, Neil M.
Drakeley, Chris J.
Ghani, Azra C.
author_sort Pothin, Emilie
collection PubMed
description BACKGROUND: Serological data are increasingly being used to monitor malaria transmission intensity and have been demonstrated to be particularly useful in areas of low transmission where traditional measures such as EIR and parasite prevalence are limited. The seroconversion rate (SCR) is usually estimated using catalytic models in which the measured antibody levels are used to categorize individuals as seropositive or seronegative. One limitation of this approach is the requirement to impose a fixed cut-off to distinguish seropositive and negative individuals. Furthermore, the continuous variation in antibody levels is ignored thereby potentially reducing the precision of the estimate. METHODS: An age-specific density model which mimics antibody acquisition and loss was developed to make full use of the information provided by serological measures of antibody levels. This was fitted to blood-stage antibody density data from 12 villages at varying transmission intensity in Northern Tanzania to estimate the exposure rate as an alternative measure of transmission intensity. RESULTS: The results show a high correlation between the exposure rate estimates obtained and the estimated SCR obtained from a catalytic model (r = 0.95) and with two derived measures of EIR (r = 0.74 and r = 0.81). Estimates of exposure rate obtained with the density model were also more precise than those derived from catalytic models. CONCLUSION: This approach, if validated across different epidemiological settings, could be a useful alternative framework for quantifying transmission intensity, which makes more complete use of serological data.
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spelling pubmed-47485472016-02-11 Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models Pothin, Emilie Ferguson, Neil M. Drakeley, Chris J. Ghani, Azra C. Malar J Methodology BACKGROUND: Serological data are increasingly being used to monitor malaria transmission intensity and have been demonstrated to be particularly useful in areas of low transmission where traditional measures such as EIR and parasite prevalence are limited. The seroconversion rate (SCR) is usually estimated using catalytic models in which the measured antibody levels are used to categorize individuals as seropositive or seronegative. One limitation of this approach is the requirement to impose a fixed cut-off to distinguish seropositive and negative individuals. Furthermore, the continuous variation in antibody levels is ignored thereby potentially reducing the precision of the estimate. METHODS: An age-specific density model which mimics antibody acquisition and loss was developed to make full use of the information provided by serological measures of antibody levels. This was fitted to blood-stage antibody density data from 12 villages at varying transmission intensity in Northern Tanzania to estimate the exposure rate as an alternative measure of transmission intensity. RESULTS: The results show a high correlation between the exposure rate estimates obtained and the estimated SCR obtained from a catalytic model (r = 0.95) and with two derived measures of EIR (r = 0.74 and r = 0.81). Estimates of exposure rate obtained with the density model were also more precise than those derived from catalytic models. CONCLUSION: This approach, if validated across different epidemiological settings, could be a useful alternative framework for quantifying transmission intensity, which makes more complete use of serological data. BioMed Central 2016-02-09 /pmc/articles/PMC4748547/ /pubmed/26861862 http://dx.doi.org/10.1186/s12936-016-1121-0 Text en © Pothin et al. 2016 Open AccessThis 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 Methodology
Pothin, Emilie
Ferguson, Neil M.
Drakeley, Chris J.
Ghani, Azra C.
Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title_full Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title_fullStr Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title_full_unstemmed Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title_short Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
title_sort estimating malaria transmission intensity from plasmodium falciparum serological data using antibody density models
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748547/
https://www.ncbi.nlm.nih.gov/pubmed/26861862
http://dx.doi.org/10.1186/s12936-016-1121-0
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