Cargando…

Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection

BACKGROUND: In areas where malaria endemicity is high, many people harbour blood stage parasites without acute febrile illness, complicating the estimation of disease burden from infection data. For Plasmodium falciparum the density of parasitaemia that can be tolerated is low in the youngest childr...

Descripción completa

Detalles Bibliográficos
Autores principales: Müller, Ivo, Genton, Blaise, Rare, Lawrence, Kiniboro, Benson, Kastens, Will, Zimmerman, Peter, Kazura, James, Alpers, Michael, Smith, Thomas A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719654/
https://www.ncbi.nlm.nih.gov/pubmed/19602275
http://dx.doi.org/10.1186/1475-2875-8-158
_version_ 1782170087240761344
author Müller, Ivo
Genton, Blaise
Rare, Lawrence
Kiniboro, Benson
Kastens, Will
Zimmerman, Peter
Kazura, James
Alpers, Michael
Smith, Thomas A
author_facet Müller, Ivo
Genton, Blaise
Rare, Lawrence
Kiniboro, Benson
Kastens, Will
Zimmerman, Peter
Kazura, James
Alpers, Michael
Smith, Thomas A
author_sort Müller, Ivo
collection PubMed
description BACKGROUND: In areas where malaria endemicity is high, many people harbour blood stage parasites without acute febrile illness, complicating the estimation of disease burden from infection data. For Plasmodium falciparum the density of parasitaemia that can be tolerated is low in the youngest children, but reaches a maximum in the age groups at highest risk of infection. There is little data on the age dependence of tolerance in other species of human malaria. METHODS: Parasite densities measured in 24,386 presumptive malaria cases at two local health centres in the Wosera area of Papua New Guinea were compared with the distributions of parasite densities recorded in community surveys in the same area. We then analyse the proportions of cases attributable to each of Plasmodium falciparum, P. vivax, and P. malariae as functions of parasite density and age using a latent class model. These attributable fractions are then used to compute the incidence of attributable disease. RESULTS: Overall 33.3%, 6.1%, and 0.1% of the presumptive cases were attributable to P. falciparum, P. vivax, and P. malariae respectively. The incidence of attributable disease and parasite density broadly follow similar age patterns. The logarithm of the incidence of acute illness is approximately proportion to the logarithm of the parasite density for all three malaria species, with little age variation in the relationship for P. vivax or P. malariae. P. falciparum shows more age variation in disease incidence at given levels of parasitaemia than the other species. CONCLUSION: The similarities between Plasmodium species in the relationships between parasite density and risk of attributable disease are compatible with the hypothesis that pan-specific mechanisms may regulate tolerance to different human Plasmodia. A straightforward mathematical expression might be used to project disease burden from parasite density distributions assessed in community-based parasitological surveys.
format Text
id pubmed-2719654
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-27196542009-08-01 Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection Müller, Ivo Genton, Blaise Rare, Lawrence Kiniboro, Benson Kastens, Will Zimmerman, Peter Kazura, James Alpers, Michael Smith, Thomas A Malar J Research BACKGROUND: In areas where malaria endemicity is high, many people harbour blood stage parasites without acute febrile illness, complicating the estimation of disease burden from infection data. For Plasmodium falciparum the density of parasitaemia that can be tolerated is low in the youngest children, but reaches a maximum in the age groups at highest risk of infection. There is little data on the age dependence of tolerance in other species of human malaria. METHODS: Parasite densities measured in 24,386 presumptive malaria cases at two local health centres in the Wosera area of Papua New Guinea were compared with the distributions of parasite densities recorded in community surveys in the same area. We then analyse the proportions of cases attributable to each of Plasmodium falciparum, P. vivax, and P. malariae as functions of parasite density and age using a latent class model. These attributable fractions are then used to compute the incidence of attributable disease. RESULTS: Overall 33.3%, 6.1%, and 0.1% of the presumptive cases were attributable to P. falciparum, P. vivax, and P. malariae respectively. The incidence of attributable disease and parasite density broadly follow similar age patterns. The logarithm of the incidence of acute illness is approximately proportion to the logarithm of the parasite density for all three malaria species, with little age variation in the relationship for P. vivax or P. malariae. P. falciparum shows more age variation in disease incidence at given levels of parasitaemia than the other species. CONCLUSION: The similarities between Plasmodium species in the relationships between parasite density and risk of attributable disease are compatible with the hypothesis that pan-specific mechanisms may regulate tolerance to different human Plasmodia. A straightforward mathematical expression might be used to project disease burden from parasite density distributions assessed in community-based parasitological surveys. BioMed Central 2009-07-14 /pmc/articles/PMC2719654/ /pubmed/19602275 http://dx.doi.org/10.1186/1475-2875-8-158 Text en Copyright © 2009 Müller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Müller, Ivo
Genton, Blaise
Rare, Lawrence
Kiniboro, Benson
Kastens, Will
Zimmerman, Peter
Kazura, James
Alpers, Michael
Smith, Thomas A
Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title_full Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title_fullStr Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title_full_unstemmed Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title_short Three different Plasmodium species show similar patterns of clinical tolerance of malaria infection
title_sort three different plasmodium species show similar patterns of clinical tolerance of malaria infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719654/
https://www.ncbi.nlm.nih.gov/pubmed/19602275
http://dx.doi.org/10.1186/1475-2875-8-158
work_keys_str_mv AT mullerivo threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT gentonblaise threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT rarelawrence threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT kiniborobenson threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT kastenswill threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT zimmermanpeter threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT kazurajames threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT alpersmichael threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection
AT smiththomasa threedifferentplasmodiumspeciesshowsimilarpatternsofclinicaltoleranceofmalariainfection