Urinary Disease in 2 Dogon Populations with Different Exposure to Schistosoma haematobium Infection: Progression of Bladder and Kidney Diseases in Children and Adults
BackgroundSchistosoma haematobium infection causes severe urinary disease and considerable mortality. The factors that determine disease progression from mild to severe stages are not fully understood MethodsHere we describe a cross-sectional epidemiological study of kidney and bladder diseases in 2...
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Published in | The Journal of infectious diseases Vol. 192; no. 12; pp. 2152 - 2159 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
15.12.2005
University of Chicago Press Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | BackgroundSchistosoma haematobium infection causes severe urinary disease and considerable mortality. The factors that determine disease progression from mild to severe stages are not fully understood MethodsHere we describe a cross-sectional epidemiological study of kidney and bladder diseases in 2 Dogon populations with different exposure to S. haematobium infection ResultsEarly and high exposure resulted in more-severe disease, especially among young subjects, without clear evidence of a more-rapid development of immunity. Nevertheless, 50%–60% of subjects of all age classes in both villages showed no evidence of disease. Kidney and bladder disease peaked biphasically among young subjects and adults >25 years old. The first peak corresponded with infections of maximum intensity, whereas the second peak occurred among adults with infections of very low intensity. Kidney disease was correlated with circulating anodic antigen concentration in serum, whereas bladder disease was correlated with egg count and eosinophil cationic protein concentration in urine. Kidney and bladder disease did not correlate. Severe kidney disease was more frequent in certain families ConclusionsThe frequency of urinary disease is increased by infections acquired early during life, is regulated by strong clinical immunity in certain subjects, and may be dependent on hereditary factors. Kidney and bladder disease may involve different mechanisms of pathogenesis, which may differ between children and adults |
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Bibliography: | ark:/67375/HXZ-4HQ9K6R9-B istex:E590A2807EFEC7D057221EAA55829C54C363F049 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1086/498214 |