Estimating individual exposure to malaria using local prevalence of malaria infection in the field.
BACKGROUND:Heterogeneity in malaria exposure complicates survival analyses of vaccine efficacy trials and confounds the association between immune correlates of protection and malaria infection in longitudinal studies. Analysis may be facilitated by taking into account the variability in individual...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2012-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3315550?pdf=render |
_version_ | 1818984099492134912 |
---|---|
author | Ally Olotu Gregory Fegan Juliana Wambua George Nyangweso Edna Ogada Chris Drakeley Kevin Marsh Philip Bejon |
author_facet | Ally Olotu Gregory Fegan Juliana Wambua George Nyangweso Edna Ogada Chris Drakeley Kevin Marsh Philip Bejon |
author_sort | Ally Olotu |
collection | DOAJ |
description | BACKGROUND:Heterogeneity in malaria exposure complicates survival analyses of vaccine efficacy trials and confounds the association between immune correlates of protection and malaria infection in longitudinal studies. Analysis may be facilitated by taking into account the variability in individual exposure levels, but it is unclear how exposure can be estimated at an individual level. METHOD AND FINDINGS:We studied three cohorts (Chonyi, Junju and Ngerenya) in Kilifi District, Kenya to assess measures of malaria exposure. Prospective data were available on malaria episodes, geospatial coordinates, proximity to infected and uninfected individuals and residence in predefined malaria hotspots for 2,425 individuals. Antibody levels to the malaria antigens AMA1 and MSP1(142) were available for 291 children from Junju. We calculated distance-weighted local prevalence of malaria infection within 1 km radius as a marker of individual's malaria exposure. We used multivariable modified Poisson regression model to assess the discriminatory power of these markers for malaria infection (i.e. asymptomatic parasitaemia or clinical malaria). The area under the receiver operating characteristic (ROC) curve was used to assess the discriminatory power of the models. Local malaria prevalence within 1 km radius and AMA1 and MSP1(142) antibodies levels were independently associated with malaria infection. Weighted local malaria prevalence had an area under ROC curve of 0.72 (95%CI: 0.66-0.73), 0.71 (95%CI: 0.69-0.73) and 0.82 (95%CI: 0.80-0.83) among cohorts in Chonyi, Junju and Ngerenya respectively. In a small subset of children from Junju, a model incorporating weighted local malaria prevalence with AMA1 and MSP1(142) antibody levels provided an AUC of 0.83 (95%CI: 0.79-0.88). CONCLUSION:We have proposed an approach to estimating the intensity of an individual's malaria exposure in the field. The weighted local malaria prevalence can be used as individual marker of malaria exposure in malaria vaccine trials and longitudinal studies of natural immunity to malaria. |
first_indexed | 2024-12-20T18:13:37Z |
format | Article |
id | doaj.art-518fbe6477ab408bbfb2e3355b099b01 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-20T18:13:37Z |
publishDate | 2012-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-518fbe6477ab408bbfb2e3355b099b012022-12-21T19:30:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3292910.1371/journal.pone.0032929Estimating individual exposure to malaria using local prevalence of malaria infection in the field.Ally OlotuGregory FeganJuliana WambuaGeorge NyangwesoEdna OgadaChris DrakeleyKevin MarshPhilip BejonBACKGROUND:Heterogeneity in malaria exposure complicates survival analyses of vaccine efficacy trials and confounds the association between immune correlates of protection and malaria infection in longitudinal studies. Analysis may be facilitated by taking into account the variability in individual exposure levels, but it is unclear how exposure can be estimated at an individual level. METHOD AND FINDINGS:We studied three cohorts (Chonyi, Junju and Ngerenya) in Kilifi District, Kenya to assess measures of malaria exposure. Prospective data were available on malaria episodes, geospatial coordinates, proximity to infected and uninfected individuals and residence in predefined malaria hotspots for 2,425 individuals. Antibody levels to the malaria antigens AMA1 and MSP1(142) were available for 291 children from Junju. We calculated distance-weighted local prevalence of malaria infection within 1 km radius as a marker of individual's malaria exposure. We used multivariable modified Poisson regression model to assess the discriminatory power of these markers for malaria infection (i.e. asymptomatic parasitaemia or clinical malaria). The area under the receiver operating characteristic (ROC) curve was used to assess the discriminatory power of the models. Local malaria prevalence within 1 km radius and AMA1 and MSP1(142) antibodies levels were independently associated with malaria infection. Weighted local malaria prevalence had an area under ROC curve of 0.72 (95%CI: 0.66-0.73), 0.71 (95%CI: 0.69-0.73) and 0.82 (95%CI: 0.80-0.83) among cohorts in Chonyi, Junju and Ngerenya respectively. In a small subset of children from Junju, a model incorporating weighted local malaria prevalence with AMA1 and MSP1(142) antibody levels provided an AUC of 0.83 (95%CI: 0.79-0.88). CONCLUSION:We have proposed an approach to estimating the intensity of an individual's malaria exposure in the field. The weighted local malaria prevalence can be used as individual marker of malaria exposure in malaria vaccine trials and longitudinal studies of natural immunity to malaria.http://europepmc.org/articles/PMC3315550?pdf=render |
spellingShingle | Ally Olotu Gregory Fegan Juliana Wambua George Nyangweso Edna Ogada Chris Drakeley Kevin Marsh Philip Bejon Estimating individual exposure to malaria using local prevalence of malaria infection in the field. PLoS ONE |
title | Estimating individual exposure to malaria using local prevalence of malaria infection in the field. |
title_full | Estimating individual exposure to malaria using local prevalence of malaria infection in the field. |
title_fullStr | Estimating individual exposure to malaria using local prevalence of malaria infection in the field. |
title_full_unstemmed | Estimating individual exposure to malaria using local prevalence of malaria infection in the field. |
title_short | Estimating individual exposure to malaria using local prevalence of malaria infection in the field. |
title_sort | estimating individual exposure to malaria using local prevalence of malaria infection in the field |
url | http://europepmc.org/articles/PMC3315550?pdf=render |
work_keys_str_mv | AT allyolotu estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT gregoryfegan estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT julianawambua estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT georgenyangweso estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT ednaogada estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT chrisdrakeley estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT kevinmarsh estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield AT philipbejon estimatingindividualexposuretomalariausinglocalprevalenceofmalariainfectioninthefield |