Literature DB >> 19571748

New developments in Plasmodium vivax malaria: severe disease and the rise of chloroquine resistance.

Ric N Price1, Nicholas M Douglas, Nicholas M Anstey.   

Abstract

PURPOSE OF REVIEW: Unlike Plasmodium falciparum, Plasmodium vivax rarely causes severe disease in healthy travellers or in temperate endemic regions and has been regarded as readily treatable with chloroquine. However, in tropical areas, recent reports have highlighted severe and fatal disease associated with P. vivax infection. We review the evidence for severe disease and the spread of drug-resistant P. vivax and speculate how these maybe related. RECENT
FINDINGS: Studies from Indonesia, Papua New Guinea, Thailand and India have shown that 21-27% of patients with severe malaria have P. vivax monoinfection. The clinical spectrum of these cases is broad with an overall mortality of 0.8-1.6%. Major manifestations include severe anaemia and respiratory distress, with infants being particularly vulnerable. Most reports of severe and fatal vivax malaria come from endemic regions where populations have limited access to healthcare, a high prevalence of comorbidity and where drug-resistant P. vivax strains and partially effective primaquine regimens significantly undermine the radical cure and control of this relapsing infection. The mechanisms underlying severe disease in vivax malaria remain poorly defined.
SUMMARY: Severe, fatal and multidrug-resistant vivax malaria challenge our perception of P. vivax as a benign disease. Strategies to understand and address these phenomena are needed urgently if the global elimination of malaria is to succeed.

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Year:  2009        PMID: 19571748     DOI: 10.1097/QCO.0b013e32832f14c1

Source DB:  PubMed          Journal:  Curr Opin Infect Dis        ISSN: 0951-7375            Impact factor:   4.915


  173 in total

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Review 2.  How can we identify parasite genes that underlie antimalarial drug resistance?

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3.  Defying malaria: Fathoming severe Plasmodium vivax disease.

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Review 4.  From within host dynamics to the epidemiology of infectious disease: Scientific overview and challenges.

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5.  A 95 kDa protein of Plasmodium vivax and P. cynomolgi visualized by three-dimensional tomography in the caveola-vesicle complexes (Schüffner's dots) of infected erythrocytes is a member of the PHIST family.

Authors:  Sheila Akinyi; Eric Hanssen; Esmeralda V S Meyer; Jianlin Jiang; Cindy C Korir; Balwan Singh; Stacey Lapp; John W Barnwell; Leann Tilley; Mary R Galinski
Journal:  Mol Microbiol       Date:  2012-04-27       Impact factor: 3.501

6.  Nitric Oxide-Dependent Endothelial Dysfunction and Reduced Arginine Bioavailability in Plasmodium vivax Malaria but No Greater Increase in Intravascular Hemolysis in Severe Disease.

Authors:  Bridget E Barber; Timothy William; Matthew J Grigg; Kim A Piera; Youwei Chen; Hao Wang; J Brice Weinberg; Tsin W Yeo; Nicholas M Anstey
Journal:  J Infect Dis       Date:  2016-09-13       Impact factor: 5.226

Review 7.  Malaria-related anaemia: a Latin American perspective.

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8.  Analysis of the causes of spawning of large-scale, severe malarial epidemics and their rapid total extinction in western Provence, historically a highly endemic region of France (1745-1850).

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Review 9.  Potential immune mechanisms associated with anemia in Plasmodium vivax malaria: a puzzling question.

Authors:  Thiago Castro-Gomes; Luiza C Mourão; Gisely C Melo; Wuelton M Monteiro; Marcus V G Lacerda; Érika M Braga
Journal:  Infect Immun       Date:  2014-08-04       Impact factor: 3.441

10.  Biosynthesis of GDP-fucose and other sugar nucleotides in the blood stages of Plasmodium falciparum.

Authors:  Sílvia Sanz; Giulia Bandini; Diego Ospina; Maria Bernabeu; Karina Mariño; Carmen Fernández-Becerra; Luis Izquierdo
Journal:  J Biol Chem       Date:  2013-04-24       Impact factor: 5.157

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