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Morbidity associated with Schistosoma mansoni infection in north-eastern Democratic Republic of the Congo
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Background
Reducing morbidity is the main target of schistosomiasis control efforts, yet only rarely do control programmes assess morbidity linked to
Schistosoma
sp. infection. In the Democratic Republic of Congo (DRC), and particularly in north-eastern Ituri Province, little is known about morbidity associated with
Schistosoma mansoni
infection. For this reason, we aimed to assess intestinal and hepatosplenic morbidity associated with
S
.
mansoni
infection in Ituri Province.
Methods/Principal findings
In 2017, we conducted a cross-sectional study in 13 villages in Ituri Province, DRC.
S
.
mansoni
infection was assessed with a Kato-Katz stool test (2 smears) and a point-of-care circulating cathodic antigen (POC-CCA) urine test. A questionnaire was used to obtain demographic data and information about experienced intestinal morbidity. Each participant underwent an abdominal ultrasonography examination to diagnose hepatosplenic morbidity. Of the 586 study participants, 76.6% tested positive for
S
.
mansoni
. Intestinal morbidity reported in the two preceding weeks was very frequent, and included abdominal pain (52.7%), diarrhoea (23.4%) and blood in the stool (21.5%). Hepatosplenic morbidity consisted of abnormal liver parenchyma patterns (42.8%), hepatomegaly (26.5%) and splenomegaly (25.3%). Liver pathology (adjusted odds ratio [aOR] 1.20, 95% confidence interval [CI] 1.06–1.37,
p
= 0.005) was positively and significantly associated with
S
.
mansoni
infection. Hepatomegaly (aOR 1.52, 95% CI 0.99–2.32,
p
= 0.053) and splenomegaly (aOR 1.12, 95% CI 0.73–1.72,
p
= 0.619) were positively but not significantly associated with
S
.
mansoni
infection at the individual level. At the village level,
S
.
mansoni
prevalence was positively associated with the prevalence of hepatomegaly and splenomegaly. High-intensity
S
.
mansoni
infections were associated with diarrhoea, blood in the stool, hepatomegaly, splenomegaly, and liver parenchyma (C, D, E and F pathology patterns). Four study participants were diagnosed with ascites and five reported hematemesis.
Conclusions/Significance
Our study documents a high burden of intestinal and hepatosplenic morbidity associated with
S
.
mansoni
infection status in Ituri Province. The findings call for targeted interventions to address both
S
.
mansoni
infection and related morbidity.
Public Library of Science (PLoS)
Title: Morbidity associated with Schistosoma mansoni infection in north-eastern Democratic Republic of the Congo
Description:
Background
Reducing morbidity is the main target of schistosomiasis control efforts, yet only rarely do control programmes assess morbidity linked to
Schistosoma
sp.
infection.
In the Democratic Republic of Congo (DRC), and particularly in north-eastern Ituri Province, little is known about morbidity associated with
Schistosoma mansoni
infection.
For this reason, we aimed to assess intestinal and hepatosplenic morbidity associated with
S
.
mansoni
infection in Ituri Province.
Methods/Principal findings
In 2017, we conducted a cross-sectional study in 13 villages in Ituri Province, DRC.
S
.
mansoni
infection was assessed with a Kato-Katz stool test (2 smears) and a point-of-care circulating cathodic antigen (POC-CCA) urine test.
A questionnaire was used to obtain demographic data and information about experienced intestinal morbidity.
Each participant underwent an abdominal ultrasonography examination to diagnose hepatosplenic morbidity.
Of the 586 study participants, 76.
6% tested positive for
S
.
mansoni
.
Intestinal morbidity reported in the two preceding weeks was very frequent, and included abdominal pain (52.
7%), diarrhoea (23.
4%) and blood in the stool (21.
5%).
Hepatosplenic morbidity consisted of abnormal liver parenchyma patterns (42.
8%), hepatomegaly (26.
5%) and splenomegaly (25.
3%).
Liver pathology (adjusted odds ratio [aOR] 1.
20, 95% confidence interval [CI] 1.
06–1.
37,
p
= 0.
005) was positively and significantly associated with
S
.
mansoni
infection.
Hepatomegaly (aOR 1.
52, 95% CI 0.
99–2.
32,
p
= 0.
053) and splenomegaly (aOR 1.
12, 95% CI 0.
73–1.
72,
p
= 0.
619) were positively but not significantly associated with
S
.
mansoni
infection at the individual level.
At the village level,
S
.
mansoni
prevalence was positively associated with the prevalence of hepatomegaly and splenomegaly.
High-intensity
S
.
mansoni
infections were associated with diarrhoea, blood in the stool, hepatomegaly, splenomegaly, and liver parenchyma (C, D, E and F pathology patterns).
Four study participants were diagnosed with ascites and five reported hematemesis.
Conclusions/Significance
Our study documents a high burden of intestinal and hepatosplenic morbidity associated with
S
.
mansoni
infection status in Ituri Province.
The findings call for targeted interventions to address both
S
.
mansoni
infection and related morbidity.
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