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Physiopathologic factors resulting in poor outcome in childhood severe malaria in Cameroon
Inocent Gouado1, Joël Bertrand Pankoui M, Honoré Fotso K
1Department of Biochemistry, University of Douala, Douala, Cameroon. gouadoi@yahoo.fr
Insights
Lactate and nitric oxide (NO) levels indicate poor prognosis in pediatric malaria. While creatinine, urea, and bilirubin were not significant predictors, they can help monitor treatment response in severe cases.
Area of Science:
- Pediatric infectious diseases
- Biochemistry
- Clinical diagnostics
Background:
- Malaria remains a significant global health challenge, particularly affecting children.
- Identifying reliable biomarkers for disease severity and prognosis is crucial for effective management.
Purpose of the Study:
- To evaluate plasma levels of creatinine, urea, bilirubin, lactic acid, and nitric oxide (NO) in children with malaria.
- To identify indices that predict disease severity and fatal outcomes in pediatric malaria patients.
Main Methods:
- Plasma samples were collected from pediatric malaria patients (0-15 years).
- Spectrophotometry was used to determine levels of creatinine, urea, bilirubin, lactic acid, and nitric oxide.
- Clinical data was recorded for correlation with biochemical markers.
Main Results:
- Elevated lactate levels were observed in severe malaria groups (cerebral malaria and anemia).
- Nitric oxide (NO) levels were significantly higher in all malaria groups compared to controls, especially in severe cases.
- Creatinine, urea, and bilirubin levels were generally within normal ranges, with some exceptions for urea in specific patient subgroups.
Conclusions:
- Lactate and nitric oxide (NO) are identified as key indicators of poor prognosis in pediatric malaria.
- While not significant predictors of outcome, creatinine, urea, and bilirubin can be useful for assessing treatment response in severe malaria.
Objectives:
We evaluated plasma creatinine, urea, bilirubin, lactic acid, and nitric oxide values in children with malaria to identify indices of disease severity and predictors of fatal outcomes.
Methods:
Children 0 to 15 years old were recruited, clinical data recorded, and blood samples collected. Plasma creatinine, urea, bilirubin, lactic acid, and nitric oxide (NO) values were determined by spectrophotometry.
Results:
Values of creatinine, urea, and bilirubin were normal in all the groups except for urea in some groups (55.30 +/- 5.508 mg/dL and 60.45 +/- 15.56 mg/dL in anemia patients and those with the combined symptoms of cerebral malaria and anemia, respectively). The mean lactate values were high in severe malaria groups (0.57 +/- 0.05 g/L and 0.48 +/- 0.05 g/L in cerebral malaria and anemia patients, respectively). As for the mean NO values, they were above the normal range in all the groups, except the controls, but particularly in the severe malaria groups (68.66 +/- 7.85, 84.52 +/- 8.17, 99.57 +/- 10.48, 87.25 +/- 12.57, and 93.48 +/- 7.09 micromol/L for the control, uncomplicated malaria, anemia, cerebral malaria patients and those with the combined symptoms of cerebral malaria and anemia, respectively; P = 0.643).
Conclusions:
In this setting, lactate and NO were indicators of poor prognosis. Though the impact of creatinine, urea, and bilirubin were not found to be significant, they can still be useful to assess improvement in severe malaria cases.
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