Abstract

BackgroundLeishmaniasis is endemic in 98 countries with an estimated 350 million people at risk and approximately 2 million cases annually. Brazil is one of the most severely affected countries.MethodologyWe applied Bayesian geostatistical negative binomial models to analyze reported incidence data of cutaneous and visceral leishmaniasis in Brazil covering a 10-year period (2001–2010). Particular emphasis was placed on spatial and temporal patterns. The models were fitted using integrated nested Laplace approximations to perform fast approximate Bayesian inference. Bayesian variable selection was employed to determine the most important climatic, environmental, and socioeconomic predictors of cutaneous and visceral leishmaniasis.Principal FindingsFor both types of leishmaniasis, precipitation and socioeconomic proxies were identified as important risk factors. The predicted number of cases in 2010 were 30,189 (standard deviation [SD]: 7,676) for cutaneous leishmaniasis and 4,889 (SD: 288) for visceral leishmaniasis. Our risk maps predicted the highest numbers of infected people in the states of Minas Gerais and Pará for visceral and cutaneous leishmaniasis, respectively.Conclusions/SignificanceOur spatially explicit, high-resolution incidence maps identified priority areas where leishmaniasis control efforts should be targeted with the ultimate goal to reduce disease incidence.

Highlights

  • IntroductionThe parasites are transmitted by female phlebotomine sandflies and the disease occurs in human in two different clinical forms: (i) cutaneous (CL, referring to the greater group of American tegumentary leishmaniasis), which causes skin or mucosal lesion; and (ii) visceral (VL), which affects organs such as the liver and spleen [1]

  • Leishmaniasis is a group of neglected tropical diseases that are caused by parasites of the genus Leishmania

  • Almost 90% of these cases are due to cutaneous leishmaniasis, whereas the remaining 10% are due to visceral leishmaniasis

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Summary

Introduction

The parasites are transmitted by female phlebotomine sandflies and the disease occurs in human in two different clinical forms: (i) cutaneous (CL, referring to the greater group of American tegumentary leishmaniasis), which causes skin or mucosal lesion; and (ii) visceral (VL), which affects organs such as the liver and spleen [1]. The latter, if not diagnosed and treated in the early stages, is usually fatal [2,3].

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