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Plasma Plasmodium falciparum Histidine-Rich Protein-2 concentrations in children with malaria infections of differing severity in Kilifi, Kenya

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Title: Plasma Plasmodium falciparum Histidine-Rich Protein-2 concentrations in children with malaria infections of differing severity in Kilifi, Kenya
Authors: Uyoga, S
Wanjiku, P
Rop, J
Makale, J
Macharia, A
Nyutu, G
Shebbe, M
Awuondo, K
Mturi, N
Woodrow, C
Dondorp, A
Maitland, K
Williams, T
Williams, TN
Item 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.
Issue Date: 9-Aug-2020
Date of Acceptance: 31-Jul-2020
URI: http://hdl.handle.net/10044/1/82166
DOI: 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.
Sponsor/Funder: Wellcome Trust
Wellcome Trust
Wellcome Trust
Wellcome Trust
Funder's Grant Number: 091758/B/10/Z
203077/Z/16/Z (C161)
202800/Z/16/Z
203077/C/16/Z
Keywords: PfHRP2
Plasmodium falciparum histidine-rich protein-2
malaria
parasite biomass
sequestration
Microbiology
06 Biological Sciences
11 Medical and Health Sciences
Publication Status: Published
Online Publication Date: 2020-08-09
Appears in Collections:Department of Surgery and Cancer
Department of Infectious Diseases
Faculty of Medicine



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