Two-year impact of praziquantel treatment for Schistosoma japonicum infection in China: re-infection, subclinical disease and fibrosis marker measurements
Ys. Li et al., Two-year impact of praziquantel treatment for Schistosoma japonicum infection in China: re-infection, subclinical disease and fibrosis marker measurements, T RS TROP M, 94(2), 2000, pp. 191-197
Citations number
39
Categorie Soggetti
Medical Research General Topics
Journal title
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE
We studied a community cohort of 193 individuals exposed to endemic Schisto
soma japonicum infection in the Dongting Lake region of China to assess sub
clinical morbidity and the 2-year benefit of curative therapy (praziquantel
) administered in 1996. Prevalence and intensity of S. japonicum infection
before treatment were 28% and 192 eggs per gram faeces (epg), respectively.
Two years after cure, 22% of the cohort were reinfected, but with a lighte
r intensity (67 epg). Sixty-four subjects (37%) showed significant improvem
ent in ultrasound parenchyma images after treatment and 51 subjects (54%) s
howed significant improvement of periportal fibrosis. Left-lobe enlargement
also reversed (P < 0.05) and splenomegaly reversed in 6 of 8 cases and dev
eloped in only 1. Two years post-treatment a dilated portal vein became les
s frequent, but the decline was not significant (16% vs 11%, P > 0.05). The
serum levels of laminin and collagen IV associated with reinfection and in
tensity and hyaluronic acid levels correlated with ultrasound findings (P <
0.01). Overall, treatment induced a marked decrease in subclinical hepatos
plenic morbidity attributable to S. japonicum although low-intensity re-inf
ection after treatment remained relatively frequent. Stratified analysis an
d logistic models evaluated potential confounding factors for assessment of
treatment effects on hepatic fibrosis. S. japonicum infection and moderate
-heavy alcohol intake interacted: improvement in parenchymal morbidity was
impeded among drinkers (P < 0.05). Chemotherapy focused on at-risk resident
s controls prevalent subclinical hepatic fibrosis but re-infection indicate
s the need for complementary control strategies.