Abstract

Endemic throughout Latin America with a prevalence rate of approximately 1.4%, Chagas disease (CD) is estimated to kill 14,000 people every year, which is more people in the region each year than any other parasite-born disease, including malaria [1],[2]. Brazilian physician Carlos Chagas first described CD exactly a century ago [3], and its socioeconomic impact makes it the most important parasitic disease in the Americas [4]. Estimated to infect somewhere between 8 to 14 million people, CD both afflicts the poor and, like other neglected tropical diseases, “promotes poverty” [2],[5]. Through its impact on worker productivity, and by causing premature disability and death, CD annually costs an estimated 667,000 disability-adjusted life years lost [1],[6]. In the case of Brazil alone, losses of over US$1.3 billion in wages and industrial productivity were due to the disabilities of workers with CD [7]. CD is an important public health issue, both in Latin America and increasingly around the world: the infection rate in endemic areas is estimated to be 1.4% [8], with geographic variation from 0.1% to 45.2% [9]. Vectorial transmission has been significantly reduced due to control efforts like the Southern Cone Initiative [10],[11] and others [11],[12]. However, there are areas producing new cases such as regions untouched by vector control efforts [13], special areas with non-domiciliated triatomine [14], and the Amazon region with recent cases reported via oral transmission and by wild triatomine [15]. And still to this day, millions of patients remain without adequate treatment for this silently debilitating and potentially fatal disease. Although no official global figures exist, it is estimated that no more than 1% of those infected are believed to receive any treatment at all. An increasing number of CD patients are also seen in non-endemic, developed countries because of globalization and the movement of unknowingly infected people from Latin America to other parts of the world [16],[17],[18]. The appearance of Trypanosoma cruzi in blood banks in the United States has led the Food and Drug Administration (FDA) to recently issue a draft guidance on CD screening [19].

Highlights

  • Endemic throughout Latin America with a prevalence rate of approximately 1.4%, Chagas disease (CD) is estimated to kill 14,000 people every year, which is more people in the region each year than any other parasite-born disease, including malaria [1,2]

  • Caused by infection with the protozoan parasite T. cruzi, CD starts with an acute phase in which the parasitemia is often high and parasitological diagnosis can be made by direct microscopic examination of fresh blood

  • Difficult challenges lie ahead in the quest for the elimination of CD, as was acknowledged by the World Health Organization (WHO) in its recent report to the World Health Assembly [35], even as several new initiatives emerge on both the control and the research landscape

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Summary

Introduction

Endemic throughout Latin America with a prevalence rate of approximately 1.4%, Chagas disease (CD) is estimated to kill 14,000 people every year, which is more people in the region each year than any other parasite-born disease, including malaria [1,2]. There are areas producing new cases such as regions untouched by vector control efforts [13], special areas with non-domiciliated triatomine [14], and the Amazon region with recent cases reported via oral transmission and by wild triatomine [15] Still to this day, millions of patients remain without adequate treatment for this silently debilitating and potentially fatal disease. Caused by infection with the protozoan parasite T. cruzi, CD starts with an acute phase in which the parasitemia is often high and parasitological diagnosis can be made by direct microscopic examination of fresh blood This disease phase (in which 2%–8% of children die) [20,21] frequently passes undiagnosed in the absence of active screening programs, as CD manifests itself with a febrile and toxemic illness having non-specific symptoms reminiscent of any childhood infection. While some promising academic and non-commercial drug discovery efforts exist, the current drug research and development (R&D) pipeline is still very limited, with no new drug expected within the 3–4 years

Barriers to Development and Evaluation of Treatments
Filling Gaps in the Pipeline
Presentation Stability Dosing regimen
Conclusion
Findings
Supporting Information
Full Text
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