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Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination

BACKGROUND: Targeted research on residual malaria transmission is important to improve strategies in settings pursuing elimination, where transmission reductions prove challenging. This study aimed to detect and characterize spatial heterogeneity and factors associated with Plasmodium falciparum inf...

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Autores principales: Rakotondramanga, Jean Marius, Vigan-Womas, Inès, Steinhardt, Laura C., Harimanana, Aina, Ravaoarisoa, Elisabeth, Rasoloharimanana, Tsikiniaina L., Razanatsiorimalala, Seheno, Wesolowski, Amy, Randrianarivelojosia, Milijaona, Roche, Benjamin, Garchitorena, Andres
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392911/
https://www.ncbi.nlm.nih.gov/pubmed/35989358
http://dx.doi.org/10.1186/s12936-022-04260-0
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author Rakotondramanga, Jean Marius
Vigan-Womas, Inès
Steinhardt, Laura C.
Harimanana, Aina
Ravaoarisoa, Elisabeth
Rasoloharimanana, Tsikiniaina L.
Razanatsiorimalala, Seheno
Wesolowski, Amy
Randrianarivelojosia, Milijaona
Roche, Benjamin
Garchitorena, Andres
author_facet Rakotondramanga, Jean Marius
Vigan-Womas, Inès
Steinhardt, Laura C.
Harimanana, Aina
Ravaoarisoa, Elisabeth
Rasoloharimanana, Tsikiniaina L.
Razanatsiorimalala, Seheno
Wesolowski, Amy
Randrianarivelojosia, Milijaona
Roche, Benjamin
Garchitorena, Andres
author_sort Rakotondramanga, Jean Marius
collection PubMed
description BACKGROUND: Targeted research on residual malaria transmission is important to improve strategies in settings pursuing elimination, where transmission reductions prove challenging. This study aimed to detect and characterize spatial heterogeneity and factors associated with Plasmodium falciparum infections and exposure, P. falciparum apical membrane antigen 1 (PfAMA1) antibody (Ab) response, in the Central Highlands of Madagascar (CHL). METHODS: From May to July 2014, a cross-sectional school-based survey was carried out in 182 fokontany (villages) within 7 health districts of the CHL. Rapid diagnostic tests (RDTs) and a bead-based immunoassay including PfAMA1 antigen biomarker were used to estimate malaria prevalence and seroprevalence, respectively. Local Moran’s I index was used to detect spatial “hotspots”. Remotely sensed environmental data—temperature, vegetation indices, land covers, and elevation—were used in multivariable mixed-effects logistic regression models to characterize factors associated with malaria infection and cumulative exposure. RESULTS: Among 6,293 school-children ages 2–14 years surveyed, RDT prevalence was low at 0.8% (95% CI 0.6–1.1%), while PfAMA1 Ab seroprevalence was 7.0% (95% CI 6.4–7.7%). Hotspots of PfAMA1 Ab seroprevalence were observed in two districts (Ankazobe and Mandoto). Seroprevalence increased for children living > 5 km from a health centre (adjusted odds ratio (OR) = 1.6, 95% CI 1.2–2.2), and for those experiencing a fever episode in the previous 2 weeks (OR 1.7, 95% CI 1.2–2.4), but decreased at higher elevation (for each 100-m increase, OR = 0.7, 95% CI 0.6–0.8). A clear age pattern was observed whereby children 9–10 years old had an OR of 1.8 (95% CI 1.2–2.4), children 11–12 years an OR of 3.7 (95% CI 2.8–5.0), and children 13–14 years an OR of 5.7 (95% CI 4.0–8.0) for seropositivity, compared with younger children (2–8 years). CONCLUSION: The use of serology in this study provided a better understanding of malaria hotspots and associated factors, revealing a pattern of higher transmission linked to geographical barriers in health care access. The integration of antibody-assays into existing surveillance activities could improve exposure assessment, and may help to monitor the effectiveness of malaria control efforts and adapt elimination interventions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04260-0.
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spelling pubmed-93929112022-08-22 Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination Rakotondramanga, Jean Marius Vigan-Womas, Inès Steinhardt, Laura C. Harimanana, Aina Ravaoarisoa, Elisabeth Rasoloharimanana, Tsikiniaina L. Razanatsiorimalala, Seheno Wesolowski, Amy Randrianarivelojosia, Milijaona Roche, Benjamin Garchitorena, Andres Malar J Research BACKGROUND: Targeted research on residual malaria transmission is important to improve strategies in settings pursuing elimination, where transmission reductions prove challenging. This study aimed to detect and characterize spatial heterogeneity and factors associated with Plasmodium falciparum infections and exposure, P. falciparum apical membrane antigen 1 (PfAMA1) antibody (Ab) response, in the Central Highlands of Madagascar (CHL). METHODS: From May to July 2014, a cross-sectional school-based survey was carried out in 182 fokontany (villages) within 7 health districts of the CHL. Rapid diagnostic tests (RDTs) and a bead-based immunoassay including PfAMA1 antigen biomarker were used to estimate malaria prevalence and seroprevalence, respectively. Local Moran’s I index was used to detect spatial “hotspots”. Remotely sensed environmental data—temperature, vegetation indices, land covers, and elevation—were used in multivariable mixed-effects logistic regression models to characterize factors associated with malaria infection and cumulative exposure. RESULTS: Among 6,293 school-children ages 2–14 years surveyed, RDT prevalence was low at 0.8% (95% CI 0.6–1.1%), while PfAMA1 Ab seroprevalence was 7.0% (95% CI 6.4–7.7%). Hotspots of PfAMA1 Ab seroprevalence were observed in two districts (Ankazobe and Mandoto). Seroprevalence increased for children living > 5 km from a health centre (adjusted odds ratio (OR) = 1.6, 95% CI 1.2–2.2), and for those experiencing a fever episode in the previous 2 weeks (OR 1.7, 95% CI 1.2–2.4), but decreased at higher elevation (for each 100-m increase, OR = 0.7, 95% CI 0.6–0.8). A clear age pattern was observed whereby children 9–10 years old had an OR of 1.8 (95% CI 1.2–2.4), children 11–12 years an OR of 3.7 (95% CI 2.8–5.0), and children 13–14 years an OR of 5.7 (95% CI 4.0–8.0) for seropositivity, compared with younger children (2–8 years). CONCLUSION: The use of serology in this study provided a better understanding of malaria hotspots and associated factors, revealing a pattern of higher transmission linked to geographical barriers in health care access. The integration of antibody-assays into existing surveillance activities could improve exposure assessment, and may help to monitor the effectiveness of malaria control efforts and adapt elimination interventions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04260-0. BioMed Central 2022-08-21 /pmc/articles/PMC9392911/ /pubmed/35989358 http://dx.doi.org/10.1186/s12936-022-04260-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Rakotondramanga, Jean Marius
Vigan-Womas, Inès
Steinhardt, Laura C.
Harimanana, Aina
Ravaoarisoa, Elisabeth
Rasoloharimanana, Tsikiniaina L.
Razanatsiorimalala, Seheno
Wesolowski, Amy
Randrianarivelojosia, Milijaona
Roche, Benjamin
Garchitorena, Andres
Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title_full Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title_fullStr Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title_full_unstemmed Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title_short Identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
title_sort identification of factors associated with residual malaria transmission using school-based serological surveys in settings pursuing elimination
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392911/
https://www.ncbi.nlm.nih.gov/pubmed/35989358
http://dx.doi.org/10.1186/s12936-022-04260-0
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