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Clinical Trial
. 2005 May 14;330(7500):1109.
doi: 10.1136/bmj.38427.404259.8F. Epub 2005 Apr 25.

Antioxidant supplementation for the prevention of kwashiorkor in Malawian children: randomised, double blind, placebo controlled trial

Heather Ciliberto  1 , Michael Ciliberto, Andreé Briend, Per Ashorn, Dennis Bier, Mark Manary
Affiliations
Clinical Trial

Antioxidant supplementation for the prevention of kwashiorkor in Malawian children: randomised, double blind, placebo controlled trial

Heather Ciliberto et al. BMJ. .

Abstract

Objective: To evaluate the efficacy of antioxidant supplementation in preventing kwashiorkor in a population of Malawian children at high risk of developing kwashiorkor.

Design: Prospective, double blind, placebo controlled trial randomised by household.

Setting: 8 villages in rural southern Malawi.

Participants: 2372 children in 2156 households aged 1-4 years were enrolled; 2332 completed the trial.

Intervention: Daily supplementation with an antioxidant powder containing riboflavin, vitamin E, selenium, and N-acetylcysteine in a dose that provided about three times the recommended dietary allowance of each nutrient or placebo for 20 weeks.

Main outcome measures: The primary outcome was the incidence of oedema. Secondary outcomes were the rates of change for weight and length and the number of days of infectious symptoms.

Results: 62 children developed kwashiorkor (defined by the presence of oedema); 39/1184 (3.3%) were in the antioxidant group and 23/1188 (1.9%) were in the placebo group (relative risk 1.70, 95% confidence interval 0.98 to 2.42). The two groups did not differ in rates of weight or height gain. Children who received antioxidant supplementation did not experience less fever, cough, or diarrhoea.

Conclusions: Antioxidant supplementation at the dose provided did not prevent the onset of kwashiorkor. This finding does not support the hypothesis that depletion of vitamin E, selenium, cysteine, or riboflavin has a role in the development of kwashiorkor.

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Figures

Figure 1
Figure 1
Flow of participants through the trial
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References

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