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The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau

BACKGROUND: Vitamin A supplementation (VAS) given to children between 6 months and 5 years of age is known to reduce mortality in low-income countries. We have previously observed that girls benefit more from a lower dose of VAS than the one recommended by WHO, the effect being strongest if diphther...

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Autores principales: Yakymenko, Dorthe, Benn, Christine S, Martins, Cesario, Diness, Birgitte R, Fisker, Ane B, Rodrigues, Amabelia, Aaby, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175170/
https://www.ncbi.nlm.nih.gov/pubmed/21884606
http://dx.doi.org/10.1186/1471-2431-11-77
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author Yakymenko, Dorthe
Benn, Christine S
Martins, Cesario
Diness, Birgitte R
Fisker, Ane B
Rodrigues, Amabelia
Aaby, Peter
author_facet Yakymenko, Dorthe
Benn, Christine S
Martins, Cesario
Diness, Birgitte R
Fisker, Ane B
Rodrigues, Amabelia
Aaby, Peter
author_sort Yakymenko, Dorthe
collection PubMed
description BACKGROUND: Vitamin A supplementation (VAS) given to children between 6 months and 5 years of age is known to reduce mortality in low-income countries. We have previously observed that girls benefit more from a lower dose of VAS than the one recommended by WHO, the effect being strongest if diphtheria-tetanus-pertussis vaccine (DTP) was the most recent vaccination. We aimed to test these observations. METHODS: During national immunisations days in Guinea-Bissau, West Africa, combining oral polio vaccination and VAS, we randomised 8626 children between 6 months and 5 years of age to receive the dose of VAS recommended by WHO or half this dose. Mortality rate ratios (MRRs) were assessed after 6 and 12 month. RESULTS: The overall mortality rate among participants was lower than expected. There was no significant difference in mortality at 6 months and 12 months of follow up between the low dose VAS group and the recommended dose VAS group. The MRRs were 1.23 (0.60-2.54) after 6 months and 1.17 (0.73-1.87) after 12 months. This tendency was similar in boys and girls. The low dose was not associated with lower mortality in girls if the most recent vaccine was DTP (MRR = 0.60 (0.14-2.50) after 6 months). CONCLUSION: Our sample size does not permit firm conclusions since mortality was lower than expected. We could not confirm a beneficial effect of a lower dose of VAS on mortality in girls. TRIAL REGISTRATION: The study was registered under clinicaltrials.gov, number NCT00168636
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spelling pubmed-31751702011-09-18 The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau Yakymenko, Dorthe Benn, Christine S Martins, Cesario Diness, Birgitte R Fisker, Ane B Rodrigues, Amabelia Aaby, Peter BMC Pediatr Research Article BACKGROUND: Vitamin A supplementation (VAS) given to children between 6 months and 5 years of age is known to reduce mortality in low-income countries. We have previously observed that girls benefit more from a lower dose of VAS than the one recommended by WHO, the effect being strongest if diphtheria-tetanus-pertussis vaccine (DTP) was the most recent vaccination. We aimed to test these observations. METHODS: During national immunisations days in Guinea-Bissau, West Africa, combining oral polio vaccination and VAS, we randomised 8626 children between 6 months and 5 years of age to receive the dose of VAS recommended by WHO or half this dose. Mortality rate ratios (MRRs) were assessed after 6 and 12 month. RESULTS: The overall mortality rate among participants was lower than expected. There was no significant difference in mortality at 6 months and 12 months of follow up between the low dose VAS group and the recommended dose VAS group. The MRRs were 1.23 (0.60-2.54) after 6 months and 1.17 (0.73-1.87) after 12 months. This tendency was similar in boys and girls. The low dose was not associated with lower mortality in girls if the most recent vaccine was DTP (MRR = 0.60 (0.14-2.50) after 6 months). CONCLUSION: Our sample size does not permit firm conclusions since mortality was lower than expected. We could not confirm a beneficial effect of a lower dose of VAS on mortality in girls. TRIAL REGISTRATION: The study was registered under clinicaltrials.gov, number NCT00168636 BioMed Central 2011-09-01 /pmc/articles/PMC3175170/ /pubmed/21884606 http://dx.doi.org/10.1186/1471-2431-11-77 Text en Copyright ©2011 Yakymenko et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yakymenko, Dorthe
Benn, Christine S
Martins, Cesario
Diness, Birgitte R
Fisker, Ane B
Rodrigues, Amabelia
Aaby, Peter
The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title_full The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title_fullStr The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title_full_unstemmed The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title_short The impact of different doses of vitamin A supplementation on male and female mortality. A randomised trial from Guinea-Bissau
title_sort impact of different doses of vitamin a supplementation on male and female mortality. a randomised trial from guinea-bissau
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175170/
https://www.ncbi.nlm.nih.gov/pubmed/21884606
http://dx.doi.org/10.1186/1471-2431-11-77
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