Risk factors for Plasmodium falciparum and Plasmodium vivax gametocyte carriage in Papua New Guinean children with uncomplicated malaria

被引:10
|
作者
Karl, Stephan [1 ,2 ]
Laman, Moses [3 ]
Moore, Brioni R. [4 ]
Benjamin, John M. [3 ]
Salib, Mary [3 ]
Lorry, Lina [3 ]
Maripal, Samuel [3 ]
Siba, Peter [3 ]
Robinson, Leanne J. [1 ,2 ,3 ]
Mueller, Ivo [1 ,2 ]
Davis, Timothy M. E. [4 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Populat Hlth & Immun Div, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Med Biol, Melbourne, Vic, Australia
[3] Papua New Guinea Inst Med Res, Madang, Papua N Guinea
[4] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Plasmodium falciparum; Plasmodium vivax; Gametocytes; Risk factors; Artemisinin combination therapy; Children; SULFADOXINE-PYRIMETHAMINE; DIHYDROARTEMISININ-PIPERAQUINE; ARTEMISININ-NAPHTHOQUINE; ARTEMETHER-LUMEFANTRINE; RANDOMIZED-TRIAL; ENDEMIC AREA; TRANSMISSION; INFECTIVITY; PRIMAQUINE; EPIDEMIOLOGY;
D O I
10.1016/j.actatropica.2016.04.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
There are limited data on gametocytaemia risk factors before/after treatment with artemisinin combination therapy in children from areas with transmission of multiple Plasmodium species. We utilised data from a randomised trial comparing artemether-lumefantrine (AL) and artemisinin-naphthoquine (AN) in 230 Papua New Guinean children aged 0.5-5 years with uncomplicated malaria in whom determinants of gametocytaemia by light microscopy were assessed at baseline using logistic regression and during follow-up using multilevel mixed effects modelling. Seventy-four (32%) and 18 (8%) children presented with P. falciparum and P. vivax gametocytaemia, respectively. Baseline P. falciparum gametocytaemia was associated with Hackett spleen grade 1 (odds ratio (95% CI) 4.01 (1.60-10.05) vs grade 0; P < 0.001) and haemoglobin (0.95 (0.92-0.97) per 1 g/L increase; P < 0.001), and P. falciparum asexual parasitaemia in slide-positive cases (0.36 (0.19-0.68) for a 10-fold increase; P = 0.002). Baseline P. vivax gametocytaemia was associated with Hackett grade 2 (12.66 (1.31-122.56); P = 0.028), mixed P. falciparum/vivax infection (0.16 (0.03-1.00); P = 0.050), P. vivax asexual parasitaemia (5.68 (0.98-33.04); P = 0.053) and haemoglobin (0.94 (0.88-1.00); P = 0.056). For post-treatment P. falciparum gametocytaemia, independent predictors were AN vs AL treatment (4.09 (1.43-11.65)), haemoglobin (0.95 (0.93-0.97)), presence/absence of P. falciparum asexual forms (3.40 (1.66-0.68)) and day post-treatment (0.086 (0.82-0.90)) (P < 0.001). Post-treatment P. vivax gametocytaemia was predicted by presence of P. vivax asexual forms (596 (12-28,433); P < 0.001). Consistent with slow P. falciparum gametocyte maturation, low haemoglobin, low asexual parasite density and higher spleen grading, markers of increased prior infection exposure/immunity, were strong associates of pre-treatment gametocyte positivity. The persistent inverse association between P. falciparum gametocytaemia and haemoglobin during follow-up suggests an important role for bone marrow modulation of gametocytogenesis. In P. vivax infections, baseline and post-treatment gametocyte carriage was positively related to the acute parasite burden, reflecting the close association between the development of asexual and sexual forms. (C)2016 Elsevier B.V. All rights reserved.
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页码:1 / 8
页数:8
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