TY - JOUR
T1 - Effect of vitamin A supplementation on morbidity due to Plasmodium falciparum in young children in Papua New Guinea
T2 - A randomised trial
AU - Shankar, Anuraj H.
AU - Genton, Blaise
AU - Semba, Richard D.
AU - Baisor, Moses
AU - Paino, Joseph
AU - Tamja, Steven
AU - Adiguma, Thomas
AU - Wu, Lee
AU - Rare, Lawrence
AU - Tielsch, James M.
AU - Alpers, Michael P.
AU - West, Keith P.
N1 - Funding Information:
We thank the people of North Wosera for their dedication and cooperation; the Sisters of the Kougia Catholic Mission for their active assistance and support; Manasseh Baea for logistical support; Nicky Gibson for slide reading; Daina Lai for anthropometry; William Deppsone for haematology; Dorothy Nawak for clinic work; William Wabanange for field supervision; Jack Taraika, Anita V Shankar, Gertrude Kanawe, Linda Orare, Zachary Dimber, Jane Simbrandu, Clara Pomba, Jennifer Dipmawe, Andrew Raiko, Meza Ginny, Lucy Lavi, and Sarah Paget for their contributions; the Ministry of Health of Papua New Guinea and East Sepik Province for their support; Task Force Sight and Life for supplements and placebos; Neal Alexander for the randomisation routines and advice on the analysis, Essie Yamini for analysis of retinol concentrations; Lawrence Moulton for helpful comments; and David Calder of USAID for proposing this study and for his support. This work was supported by Co-operative Agreements No. DAN 0045–A-00–5094–00 and HRN-A-00–97–00015–00 between the Johns Hopkins School of Hygiene and Public Health and the Office of Health and Nutrition, the US Agency for International Development (USAID), and an Australian Agency for International Development (AusAID) grant to the Papua New Guinea Institute of Medical Research.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 1999/7/17
Y1 - 1999/7/17
N2 - Background. Many individuals at risk of malaria also have micronutrient deficiencies that may hamper protective immunity. Vitamin A is central to normal immune function, and supplementation has been shown to lower the morbidity of some infectious diseases. We investigated the effect of vitamin A supplementation on malaria morbidity. Methods. This randomised double-blind placebo-controlled trial of vitamin A supplementation took place in a P falciparum endemic area of Papua New Guinea. Of 520 potentially eligible children aged 6-60 months, 480 were randomly assigned high-dose Vitamin A (n = 239) or placebo (n = 241), every 3 months for 13 months. Malaria morbidity was assessed through weekly community-based case detection and surveillance of patients who self-reported to the health centre. Cross-sectional surveys were also done at the beginning, middle, and end of the study to assess malariometric indicators. Analyses were by intention to treat. Findings. The number of P falciparum febrile episodes (temperature ≥ 37.5°C with a parasite count of at least 8000/μL) was 30% lower in the vitamin A group than in the placebo group (178 vs 249 episodes; relative risk 0.70 [95% CI 0.57-0.87], p = 0.0013). At the end of the study P falciparum geometric mean density was lower in the vitamin A than the placebo group (1300 [907-1863] vs 2039 [1408-2951]) as was the proportion with spleen enlargement (125/196 [64%] vs 148/207 [71%]); neither difference was significant (p = 0.093 and p = 0.075). Children aged 12-36 months benefited most, having 35% fewer febrile episodes (89 vs 141; relative risk 0.65 [14-50], p = 0.0023), 26% fewer enlarged spleens (46/79 [58%] vs 67/90 [74%], p = 0.0045), and a 68% lower parasite density (1160 [95% CI 665-2022] vs 3569 [2080-6124] p = 0.0054). Vitamin A had no consistent effect on cross-sectional indices of proportion infected or with anaemia. Interpretation. Vitamin A supplementation may be an effective low-cost strategy to lower morbidity due to P falciparum in young children. The findings suggest that clinical episodes, spleen enlargement, and parasite density are influenced by different immunological mechanisms from infection and anaemia.
AB - Background. Many individuals at risk of malaria also have micronutrient deficiencies that may hamper protective immunity. Vitamin A is central to normal immune function, and supplementation has been shown to lower the morbidity of some infectious diseases. We investigated the effect of vitamin A supplementation on malaria morbidity. Methods. This randomised double-blind placebo-controlled trial of vitamin A supplementation took place in a P falciparum endemic area of Papua New Guinea. Of 520 potentially eligible children aged 6-60 months, 480 were randomly assigned high-dose Vitamin A (n = 239) or placebo (n = 241), every 3 months for 13 months. Malaria morbidity was assessed through weekly community-based case detection and surveillance of patients who self-reported to the health centre. Cross-sectional surveys were also done at the beginning, middle, and end of the study to assess malariometric indicators. Analyses were by intention to treat. Findings. The number of P falciparum febrile episodes (temperature ≥ 37.5°C with a parasite count of at least 8000/μL) was 30% lower in the vitamin A group than in the placebo group (178 vs 249 episodes; relative risk 0.70 [95% CI 0.57-0.87], p = 0.0013). At the end of the study P falciparum geometric mean density was lower in the vitamin A than the placebo group (1300 [907-1863] vs 2039 [1408-2951]) as was the proportion with spleen enlargement (125/196 [64%] vs 148/207 [71%]); neither difference was significant (p = 0.093 and p = 0.075). Children aged 12-36 months benefited most, having 35% fewer febrile episodes (89 vs 141; relative risk 0.65 [14-50], p = 0.0023), 26% fewer enlarged spleens (46/79 [58%] vs 67/90 [74%], p = 0.0045), and a 68% lower parasite density (1160 [95% CI 665-2022] vs 3569 [2080-6124] p = 0.0054). Vitamin A had no consistent effect on cross-sectional indices of proportion infected or with anaemia. Interpretation. Vitamin A supplementation may be an effective low-cost strategy to lower morbidity due to P falciparum in young children. The findings suggest that clinical episodes, spleen enlargement, and parasite density are influenced by different immunological mechanisms from infection and anaemia.
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U2 - 10.1016/S0140-6736(98)08293-2
DO - 10.1016/S0140-6736(98)08293-2
M3 - Article
C2 - 10421302
AN - SCOPUS:0033578269
SN - 0140-6736
VL - 354
SP - 203
EP - 209
JO - Lancet
JF - Lancet
IS - 9174
ER -