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      Malaria risk assessment and mapping using satellite imagery and boosted regression trees in the Peruvian Amazon

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          Abstract

          This is the first study to assess the risk of co-endemic Plasmodium vivax and Plasmodium falciparum transmission in the Peruvian Amazon using boosted regression tree (BRT) models based on social and environmental predictors derived from satellite imagery and data. Yearly cross-validated BRT models were created to discriminate high-risk (annual parasite index API > 10 cases/1000 people) and very-high-risk for malaria (API > 50 cases/1000 people) in 2766 georeferenced villages of Loreto department, between 2010–2017 as other parts in the article (graphs, tables, and texts). Predictors were cumulative annual rainfall, forest coverage, annual forest loss, annual mean land surface temperature, normalized difference vegetation index (NDVI), normalized difference water index (NDWI), shortest distance to rivers, time to populated villages, and population density. BRT models built with predictor data of a given year efficiently discriminated the malaria risk for that year in villages (area under the ROC curve (AUC) > 0.80), and most models also effectively predicted malaria risk in the following year. Cumulative rainfall, population density and time to populated villages were consistently the top three predictors for both P. vivax and P. falciparum incidence. Maps created using the BRT models characterize the spatial distribution of the malaria incidence in Loreto and should contribute to malaria-related decision making in the area.

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          Most cited references34

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          A Proposed Tropical Rainfall Measuring Mission (TRMM) Satellite

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            Global Epidemiology of Plasmodium vivax

            Plasmodium vivax is the most widespread human malaria, putting 2.5 billion people at risk of infection. Its unique biological and epidemiological characteristics pose challenges to control strategies that have been principally targeted against Plasmodium falciparum. Unlike P. falciparum, P. vivax infections have typically low blood-stage parasitemia with gametocytes emerging before illness manifests, and dormant liver stages causing relapses. These traits affect both its geographic distribution and transmission patterns. Asymptomatic infections, high-risk groups, and resulting case burdens are described in this review. Despite relatively low prevalence measurements and parasitemia levels, along with high proportions of asymptomatic cases, this parasite is not benign. Plasmodium vivax can be associated with severe and even fatal illness. Spreading resistance to chloroquine against the acute attack, and the operational inadequacy of primaquine against the multiple attacks of relapse, exacerbates the risk of poor outcomes among the tens of millions suffering from infection each year. Without strategies accounting for these P. vivax-specific characteristics, progress toward elimination of endemic malaria transmission will be substantially impeded.
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              Identification of hot spots of malaria transmission for targeted malaria control.

              Variation in the risk of malaria within populations is a frequently described but poorly understood phenomenon. This heterogeneity creates opportunities for targeted interventions but only if hot spots of malaria transmission can be easily identified. We determined spatial patterns in malaria transmission in a district in northeastern Tanzania, using malaria incidence data from a cohort study involving infants and household-level mosquito sampling data. The parasite prevalence rates and age-specific seroconversion rates (SCRs) of antibodies against Plasmodium falciparum antigens were determined in samples obtained from people attending health care facilities. Five clusters of higher malaria incidence were detected and interpreted as hot spots of transmission. These hot spots partially overlapped with clusters of higher mosquito exposure but could not be satisfactorily predicted by a probability model based on environmental factors. Small-scale local variation in malaria exposure was detected by parasite prevalence rates and SCR estimates for samples of health care facility attendees. SCR estimates were strongly associated with local malaria incidence rates and predicted hot spots of malaria transmission with 95% sensitivity and 85% specificity. Serological markers were able to detect spatial variation in malaria transmission at the microepidemiological level, and they have the potential to form an effective method for spatial targeting of malaria control efforts.
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                Author and article information

                Contributors
                elitayoan@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                23 October 2019
                23 October 2019
                2019
                : 9
                : 15173
                Affiliations
                [1 ]ISNI 0000 0001 0805 7253, GRID grid.4861.b, Université de Liège, ; 4000 Liège, Belgium
                [2 ]ISNI 0000 0001 2294 713X, GRID grid.7942.8, Research Institute of Health and Society (IRSS), , Université catholique de Louvain, ; 1200 Brussels, Belgium
                [3 ]ISNI 0000 0001 0673 9488, GRID grid.11100.31, Institute of Tropical Medicine Alexander von Humboldt, , Universidad Peruana Cayetano Heredia, ; Lima, 15102 Peru
                [4 ]Ministry of Development and Social Inclusion, Lima, 15047 Peru
                [5 ]ISNI 0000 0001 2242 8479, GRID grid.6520.1, Namur Research Institute for Life Sciences (Narilis), , Université de Namur, ; 5000 Namur, Belgium
                [6 ]Institute of Life-Earth-Environment (ILEE), 5000 Namur, Belgium
                [7 ]National Aerospace Development Commission, Lima, 15046 Peru
                [8 ]ISNI 0000 0001 0790 3681, GRID grid.5284.b, University of Antwerp, ; 2000 Antwerp, Belgium
                [9 ]GRID grid.440594.8, Faculty of Human Medicine, , Universidad Nacional de la Amazonía Peruana, ; Loreto, 160 Peru
                [10 ]ISNI 0000 0004 0647 2148, GRID grid.424470.1, Fonds de la Recherche Scientifique (FNRS), ; 1000 Brussels, Belgium
                Author information
                http://orcid.org/0000-0002-0819-7755
                Article
                51564
                10.1038/s41598-019-51564-4
                6811674
                31645604
                1054d57e-dc2b-4ec0-97a5-ea749af52743
                © The Author(s) 2019

                Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 23 July 2019
                : 2 October 2019
                Funding
                Funded by: Peruvian National Council of Science - CONCYTEC 008-2014-FONDECYT. ARES-CDC PRD-PERU 2014-2019
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                diseases,malaria
                Uncategorized
                diseases, malaria

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