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The impact of single versus mixed Schistosoma haematobium and S. mansoni infections on morbidity profiles amongst school-children in Taveta, Kenya
被引:27
作者:
Gouvras, Anouk N.
[1
]
Kariuki, Curtis
[2
]
Koukounari, Artemis
[3
]
Norton, Alice J.
[1
]
Lange, Charles N.
[2
]
Ireri, Edmund
[5
]
Fenwick, Alan
[4
]
Mkoji, Gerald M.
[5
]
Webster, Joanne P.
[1
,4
]
机构:
[1] Univ London Imperial Coll Sci Technol & Med, DIDE, Sch Publ Hlth, London, England
[2] Natl Museums Kenya, Invertebrates Zool Sect, Nairobi, Kenya
[3] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, DIDE, MRC Ctr Outbreak Anal & Modelling, London, England
[4] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, SCI, London, England
[5] Kenya Govt Med Res Ctr, Nairobi, Kenya
关键词:
Schistosomiasis;
Schistosoma mansoni;
Schistosoma haematobium;
Coinfections;
Polyparasitism;
Human morbidity;
Kenya;
PLASMODIUM-FALCIPARUM;
EXPOSURE;
CHILDREN;
MALARIA;
ASSOCIATIONS;
RESISTANCE;
RESPONSES;
ANTIGENS;
ALBUMIN;
LIVER;
D O I:
10.1016/j.actatropica.2013.01.001
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:
Two schistosome species-Schistosoma haematobium and S. mansoni-with two very different pathological profiles (urogenital versus intestinal), are responsible for the majority of human schistosomiasis infections across sub-Saharan Africa. The aim of this study was to determine whether coinfections have an impact on species-specific morbidity measures when compared to single species infections. Children from two neighbouring schools in Taveta, Kenya were grouped by infection status, i.e. uninfected, single species infections or coinfected. Clinical examination of the liver and spleen by palpation was performed and urinary albumin levels were recorded at baseline and at 12 months after praziquantel administration. Additional ultrasonographic profiles of the children's liver, spleen and bladder were incorporated at follow-up. It was found that S. haematobium-associated urogenital morbidity was lower in the coinfected group relative to single S. haematobium infections, even when infection intensities were taken into account. We also observed an association between S. haematobium infection and liver (intestinal-associated) morbidity regardless of coinfections. The findings reported here suggest that further research should be performed on the impact of S. haematobium infections on liver morbidity as well as to determine the impact of mixed schistosome species infections on human morbidity outcomes across different endemic settings. (C) 2013 Elsevier B.V. All rights reserved.
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页码:309 / 317
页数:9
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