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The risks of malariainfection in Kenya in 2009

BACKGROUND: To design an effective strategy for the control of malaria requires a map of infection and disease risks to select appropriate suites of interventions. Advances in model based geo-statistics and malaria parasite prevalence data assemblies provide unique opportunities to redefine national...

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Autores principales: Noor, Abdisalan M, Gething, Peter W, Alegana, Victor A, Patil, Anand P, Hay, Simon I, Muchiri, Eric, Juma, Elizabeth, Snow, Robert W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783030/
https://www.ncbi.nlm.nih.gov/pubmed/19930552
http://dx.doi.org/10.1186/1471-2334-9-180
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author Noor, Abdisalan M
Gething, Peter W
Alegana, Victor A
Patil, Anand P
Hay, Simon I
Muchiri, Eric
Juma, Elizabeth
Snow, Robert W
author_facet Noor, Abdisalan M
Gething, Peter W
Alegana, Victor A
Patil, Anand P
Hay, Simon I
Muchiri, Eric
Juma, Elizabeth
Snow, Robert W
author_sort Noor, Abdisalan M
collection PubMed
description BACKGROUND: To design an effective strategy for the control of malaria requires a map of infection and disease risks to select appropriate suites of interventions. Advances in model based geo-statistics and malaria parasite prevalence data assemblies provide unique opportunities to redefine national Plasmodium falciparum risk distributions. Here we present a new map of malaria risk for Kenya in 2009. METHODS: Plasmodium falciparum parasite rate data were assembled from cross-sectional community based surveys undertaken from 1975 to 2009. Details recorded for each survey included the month and year of the survey, sample size, positivity and the age ranges of sampled population. Data were corrected to a standard age-range of two to less than 10 years (PfPR(2-10)) and each survey location was geo-positioned using national and on-line digital settlement maps. Ecological and climate covariates were matched to each PfPR(2-10 )survey location and examined separately and in combination for relationships to PfPR(2-10). Significant covariates were then included in a Bayesian geostatistical spatial-temporal framework to predict continuous and categorical maps of mean PfPR(2-10 )at a 1 × 1 km resolution across Kenya for the year 2009. Model hold-out data were used to test the predictive accuracy of the mapped surfaces and distributions of the posterior uncertainty were mapped. RESULTS: A total of 2,682 estimates of PfPR(2-10 )from surveys undertaken at 2,095 sites between 1975 and 2009 were selected for inclusion in the geo-statistical modeling. The covariates selected for prediction were urbanization; maximum temperature; precipitation; enhanced vegetation index; and distance to main water bodies. The final Bayesian geo-statistical model had a high predictive accuracy with mean error of -0.15% PfPR(2-10); mean absolute error of 0.38% PfPR(2-10); and linear correlation between observed and predicted PfPR(2-10 )of 0.81. The majority of Kenya's 2009 population (35.2 million, 86.3%) reside in areas where predicted PfPR(2-10 )is less than 5%; conversely in 2009 only 4.3 million people (10.6%) lived in areas where PfPR(2-10 )was predicted to be ≥40% and were largely located around the shores of Lake Victoria. CONCLUSION: Model based geo-statistical methods can be used to interpolate malaria risks in Kenya with precision and our model shows that the majority of Kenyans live in areas of very low P. falciparum risk. As malaria interventions go to scale effectively tracking epidemiological changes of risk demands a rigorous effort to document infection prevalence in time and space to remodel risks and redefine intervention priorities over the next 10-15 years.
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spelling pubmed-27830302009-11-26 The risks of malariainfection in Kenya in 2009 Noor, Abdisalan M Gething, Peter W Alegana, Victor A Patil, Anand P Hay, Simon I Muchiri, Eric Juma, Elizabeth Snow, Robert W BMC Infect Dis Research Article BACKGROUND: To design an effective strategy for the control of malaria requires a map of infection and disease risks to select appropriate suites of interventions. Advances in model based geo-statistics and malaria parasite prevalence data assemblies provide unique opportunities to redefine national Plasmodium falciparum risk distributions. Here we present a new map of malaria risk for Kenya in 2009. METHODS: Plasmodium falciparum parasite rate data were assembled from cross-sectional community based surveys undertaken from 1975 to 2009. Details recorded for each survey included the month and year of the survey, sample size, positivity and the age ranges of sampled population. Data were corrected to a standard age-range of two to less than 10 years (PfPR(2-10)) and each survey location was geo-positioned using national and on-line digital settlement maps. Ecological and climate covariates were matched to each PfPR(2-10 )survey location and examined separately and in combination for relationships to PfPR(2-10). Significant covariates were then included in a Bayesian geostatistical spatial-temporal framework to predict continuous and categorical maps of mean PfPR(2-10 )at a 1 × 1 km resolution across Kenya for the year 2009. Model hold-out data were used to test the predictive accuracy of the mapped surfaces and distributions of the posterior uncertainty were mapped. RESULTS: A total of 2,682 estimates of PfPR(2-10 )from surveys undertaken at 2,095 sites between 1975 and 2009 were selected for inclusion in the geo-statistical modeling. The covariates selected for prediction were urbanization; maximum temperature; precipitation; enhanced vegetation index; and distance to main water bodies. The final Bayesian geo-statistical model had a high predictive accuracy with mean error of -0.15% PfPR(2-10); mean absolute error of 0.38% PfPR(2-10); and linear correlation between observed and predicted PfPR(2-10 )of 0.81. The majority of Kenya's 2009 population (35.2 million, 86.3%) reside in areas where predicted PfPR(2-10 )is less than 5%; conversely in 2009 only 4.3 million people (10.6%) lived in areas where PfPR(2-10 )was predicted to be ≥40% and were largely located around the shores of Lake Victoria. CONCLUSION: Model based geo-statistical methods can be used to interpolate malaria risks in Kenya with precision and our model shows that the majority of Kenyans live in areas of very low P. falciparum risk. As malaria interventions go to scale effectively tracking epidemiological changes of risk demands a rigorous effort to document infection prevalence in time and space to remodel risks and redefine intervention priorities over the next 10-15 years. BioMed Central 2009-11-20 /pmc/articles/PMC2783030/ /pubmed/19930552 http://dx.doi.org/10.1186/1471-2334-9-180 Text en Copyright ©2009 Noor 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 Article
Noor, Abdisalan M
Gething, Peter W
Alegana, Victor A
Patil, Anand P
Hay, Simon I
Muchiri, Eric
Juma, Elizabeth
Snow, Robert W
The risks of malariainfection in Kenya in 2009
title The risks of malariainfection in Kenya in 2009
title_full The risks of malariainfection in Kenya in 2009
title_fullStr The risks of malariainfection in Kenya in 2009
title_full_unstemmed The risks of malariainfection in Kenya in 2009
title_short The risks of malariainfection in Kenya in 2009
title_sort risks of malariainfection in kenya in 2009
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783030/
https://www.ncbi.nlm.nih.gov/pubmed/19930552
http://dx.doi.org/10.1186/1471-2334-9-180
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