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Increased plasma lipid peroxidation in riboflavin-deficient, malaria-infected children
B S Das1, D I Thurnham, J K Patnaik
1Department of Biochemistry, Ispat General Hospital, Orissa, India.
Abstract:
Plasma lipid peroxides were measured as malonyldialdehyde (MDA) by the thiobarbituric acid (TBA) method in 75 children suffering from Plasmodium falciparum malaria. Their riboflavin status was assessed by measuring erythrocyte glutathione reductase activation coefficients (EGRACs), and values greater than 1.40 were regarded as indicating biochemical deficiency. Plasma MDA was higher (p less than 0.001) in patients than in control subjects; the concentrations were 3.65 +/- 0.70 and 1.77 +/- 0.45 mumol/L (means +/- SD), respectively. The riboflavin-deficient group had higher plasma MDA values (3.98 +/- 0.70 mumol/L) than did the nondeficient group (3.30 +/- 0.68 mumol/L, p less than 0.001). Plasma MDA concentrations correlated with EGRACs (r = 0.46, p less than 0.01) in the patients. It is proposed that riboflavin deficiency restricts regeneration of reduced glutathione making the parasitized erythrocytes more vulnerable to destructive lipid peroxidation and increasing plasma lipid hydroperoxides.
Insights
Children with malaria have higher lipid peroxidation, indicated by malondialdehyde (MDA), especially if they have a riboflavin deficiency. This deficiency may increase oxidative stress in red blood cells, making them more susceptible to damage.
Area of Science:
- Biochemistry
- Malariology
- Nutritional Science
Background:
- Plasmodium falciparum malaria is a significant global health concern.
- Oxidative stress, indicated by elevated plasma lipid peroxides like malondialdehyde (MDA), is implicated in malaria pathogenesis.
- Riboflavin (vitamin B2) is crucial for antioxidant defense systems, including glutathione regeneration.
Purpose of the Study:
- To investigate the relationship between plasma lipid peroxidation and riboflavin status in children with Plasmodium falciparum malaria.
- To determine if riboflavin deficiency exacerbates oxidative stress in malaria patients.
Main Methods:
- Plasma malondialdehyde (MDA) levels were measured using the thiobarbituric acid (TBA) method in 75 children with malaria.
- Riboflavin status was assessed by measuring erythrocyte glutathione reductase activation coefficients (EGRACs), with values >1.40 indicating deficiency.
- MDA concentrations and EGRACs were compared between malaria patients and controls, and within patient groups based on riboflavin status.
Main Results:
- Malaria patients exhibited significantly higher plasma MDA levels compared to healthy controls (3.65 ± 0.70 vs. 1.77 ± 0.45 μmol/L, p < 0.001).
- Riboflavin-deficient children with malaria had significantly higher plasma MDA levels than non-deficient children (3.98 ± 0.70 vs. 3.30 ± 0.68 μmol/L, p < 0.001).
- Plasma MDA concentrations showed a positive correlation with EGRACs in malaria patients (r = 0.46, p < 0.01).
Conclusions:
- Children with Plasmodium falciparum malaria experience increased lipid peroxidation.
- Riboflavin deficiency appears to worsen oxidative stress in malaria, potentially by impairing glutathione regeneration.
- These findings suggest that maintaining adequate riboflavin status may be important for mitigating oxidative damage in children with malaria.
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