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  5. Plasma Plasmodium falciparum Histidine-Rich Protein-2 concentrations in children with malaria infections of differing severity in Kilifi, Kenya
 
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Plasma Plasmodium falciparum Histidine-Rich Protein-2 concentrations in children with malaria infections of differing severity in Kilifi, Kenya
File(s)
ciaa1141.pdf (596.85 KB)
Published version
Author(s)
Uyoga, Sophie
Wanjiku, Perpetual
Rop, Jesse
Makale, Johnstone
Macharia, Alexander
more
Type
Journal Article
Abstract
Background

Most previous studies support a direct link between total parasite load and the clinical severity of Plasmodium falciparum malaria infections.
Methods

We estimated P. falciparum parasite loads in three groups of children with malaria infections of differing severity: (1) children with WHO-defined severe malaria (n=1,544); (2) children admitted with malaria but without features of severity (n=200) and; (3) children in the community with asymptomatic parasitemia (n=33).
Results

Peripheral parasitemias were highest in those with uncomplicated malaria (geometric mean 111,064; 95%CI 86,798-141,819 parasites/μl), being almost three times higher than those with severe malaria (39,588; 34,990-44,791 parasites/μl) and >100 times higher than in those with asymptomatic malaria (1,092; 523-2,280 parasites/μl). However, geometric mean PfHRP2 values (95% CI) increased with severity, being 7 (4-12) ng/ml in asymptomatic malaria, 843 (655-1,084) ng/ml in uncomplicated malaria and 1,369 (1,244-1,506) ng/ml in severe malaria. PfHRP2 concentrations were markedly lower in the sub-group of severe malaria patients with concomitant invasive bacterial infections (IBIs) of blood or CSF (GM 312 ng/ml; 95%CI 175-557; p<0.0001) than in those without IBIs (GM 1,439 ng/ml; 1,307-1,584; P<0.001).
Conclusions

The clinical severity of malaria infections related strongly to the total burden of P. falciparum parasites. A quantitative test for plasma concentrations of PfHRP2 could be useful in identifying children at the greatest clinical risk and to identify critically ill children in whom malaria is not the primary cause.
Date Issued
2020-08-09
Date Acceptance
2020-07-31
Citation
Clinical Infectious Diseases, 2020, 73 (7), pp.e2415-e2423
URI
http://hdl.handle.net/10044/1/82166
URL
https://academic.oup.com/cid/article/73/7/e2415/5890098
DOI
https://www.dx.doi.org/10.1093/cid/ciaa1141
ISSN
1058-4838
Publisher
Oxford University Press (OUP)
Start Page
e2415
End Page
e2423
Journal / Book Title
Clinical Infectious Diseases
Volume
73
Issue
7
Copyright Statement
© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
License URL
http://creativecommons.org/licenses/by/4.0/
Sponsor
Wellcome Trust
Wellcome Trust
Wellcome Trust
Wellcome Trust
Identifier
https://academic.oup.com/cid/article/73/7/e2415/5890098
Grant Number
091758/B/10/Z
203077/Z/16/Z (C161)
202800/Z/16/Z
203077/C/16/Z
Subjects
PfHRP2
Plasmodium falciparum histidine-rich protein-2
malaria
parasite biomass
sequestration
Microbiology
06 Biological Sciences
11 Medical and Health Sciences
Publication Status
Published
Date Publish Online
2020-08-09
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