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Highly heterogeneous residual malaria risk in western Thailand
Over the past decades, the malaria burden in Thailand has substantially declined. Most infections now originate from the national border regions. In these areas, the prevalence of asymptomatic infections is still substantial and poses a challenge for the national malaria elimination program. To dete...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996282/ https://www.ncbi.nlm.nih.gov/pubmed/30954453 http://dx.doi.org/10.1016/j.ijpara.2019.01.004 |
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author | Nguitragool, Wang Karl, Stephan White, Michael Koepfli, Cristian Felger, Ingrid Singhasivanon, Pratap Mueller, Ivo Sattabongkot, Jetsumon |
author_facet | Nguitragool, Wang Karl, Stephan White, Michael Koepfli, Cristian Felger, Ingrid Singhasivanon, Pratap Mueller, Ivo Sattabongkot, Jetsumon |
author_sort | Nguitragool, Wang |
collection | PubMed |
description | Over the past decades, the malaria burden in Thailand has substantially declined. Most infections now originate from the national border regions. In these areas, the prevalence of asymptomatic infections is still substantial and poses a challenge for the national malaria elimination program. To determine epidemiological parameters as well as risk factors for malaria infection in western Thailand, we carried out a cohort study in Kanchanaburi and Ratchaburi provinces on the Thailand-Myanmar border. Blood samples from 999 local participants were examined for malaria infection every 4 weeks between May 2013 and Jun 2014. Prevalence of Plasmodium falciparum and Plasmodium vivax was determined by quantitative PCR (qPCR) and showed a seasonal variation with values fluctuating from 1.7% to 4.2% for P. vivax and 0% to 1.3% for P. falciparum. Ninety percent of infections were asymptomatic. The annual molecular force of blood-stage infection ((mol)FOB) was estimated by microsatellite genotyping to be 0.24 new infections per person-year for P. vivax and 0.02 new infections per person-year for P. falciparum. The distribution of infections was heterogenous, that is, the vast majority of infections (>80%) were found in a small number of individuals (<8% of the study population) who tested positive at multiple timepoints. Significant risk factors were detected for P. vivax infections, including previous clinical malaria, occupation in agriculture and travel to Myanmar. In contrast, indoor residual spraying was associated with a protection from infection. These findings provide a recent landscape of malaria epidemiology and emphasize the importance of novel strategies to target asymptomatic and imported infections. |
format | Online Article Text |
id | pubmed-6996282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69962822020-02-05 Highly heterogeneous residual malaria risk in western Thailand Nguitragool, Wang Karl, Stephan White, Michael Koepfli, Cristian Felger, Ingrid Singhasivanon, Pratap Mueller, Ivo Sattabongkot, Jetsumon Int J Parasitol Article Over the past decades, the malaria burden in Thailand has substantially declined. Most infections now originate from the national border regions. In these areas, the prevalence of asymptomatic infections is still substantial and poses a challenge for the national malaria elimination program. To determine epidemiological parameters as well as risk factors for malaria infection in western Thailand, we carried out a cohort study in Kanchanaburi and Ratchaburi provinces on the Thailand-Myanmar border. Blood samples from 999 local participants were examined for malaria infection every 4 weeks between May 2013 and Jun 2014. Prevalence of Plasmodium falciparum and Plasmodium vivax was determined by quantitative PCR (qPCR) and showed a seasonal variation with values fluctuating from 1.7% to 4.2% for P. vivax and 0% to 1.3% for P. falciparum. Ninety percent of infections were asymptomatic. The annual molecular force of blood-stage infection ((mol)FOB) was estimated by microsatellite genotyping to be 0.24 new infections per person-year for P. vivax and 0.02 new infections per person-year for P. falciparum. The distribution of infections was heterogenous, that is, the vast majority of infections (>80%) were found in a small number of individuals (<8% of the study population) who tested positive at multiple timepoints. Significant risk factors were detected for P. vivax infections, including previous clinical malaria, occupation in agriculture and travel to Myanmar. In contrast, indoor residual spraying was associated with a protection from infection. These findings provide a recent landscape of malaria epidemiology and emphasize the importance of novel strategies to target asymptomatic and imported infections. Elsevier Science 2019-05 /pmc/articles/PMC6996282/ /pubmed/30954453 http://dx.doi.org/10.1016/j.ijpara.2019.01.004 Text en © 2020 The Authors. Published by Elsevier Ltd on behalf of Australian Society for Parasitology. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nguitragool, Wang Karl, Stephan White, Michael Koepfli, Cristian Felger, Ingrid Singhasivanon, Pratap Mueller, Ivo Sattabongkot, Jetsumon Highly heterogeneous residual malaria risk in western Thailand |
title | Highly heterogeneous residual malaria risk in western Thailand |
title_full | Highly heterogeneous residual malaria risk in western Thailand |
title_fullStr | Highly heterogeneous residual malaria risk in western Thailand |
title_full_unstemmed | Highly heterogeneous residual malaria risk in western Thailand |
title_short | Highly heterogeneous residual malaria risk in western Thailand |
title_sort | highly heterogeneous residual malaria risk in western thailand |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996282/ https://www.ncbi.nlm.nih.gov/pubmed/30954453 http://dx.doi.org/10.1016/j.ijpara.2019.01.004 |
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