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The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial

BACKGROUND: The Pune Maternal Nutrition Study (PMNS) was established to prospectively study the relationship of maternal nutrition to fetal growth and later cardiometabolic risk in the offspring. High homocysteine and low vitamin B12 levels in pregnancy predicted lower birthweight and higher insulin...

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Autores principales: Kumaran, Kalyanaraman, Yajnik, Pallavi, Lubree, Himangi, Joglekar, Charudatta, Bhat, Dattatray, Katre, Prachi, Joshi, Suyog, Ladkat, Rasika, Fall, Caroline, Yajnik, Chittaranjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050839/
https://www.ncbi.nlm.nih.gov/pubmed/32153821
http://dx.doi.org/10.1186/s40795-017-0143-5
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author Kumaran, Kalyanaraman
Yajnik, Pallavi
Lubree, Himangi
Joglekar, Charudatta
Bhat, Dattatray
Katre, Prachi
Joshi, Suyog
Ladkat, Rasika
Fall, Caroline
Yajnik, Chittaranjan
author_facet Kumaran, Kalyanaraman
Yajnik, Pallavi
Lubree, Himangi
Joglekar, Charudatta
Bhat, Dattatray
Katre, Prachi
Joshi, Suyog
Ladkat, Rasika
Fall, Caroline
Yajnik, Chittaranjan
author_sort Kumaran, Kalyanaraman
collection PubMed
description BACKGROUND: The Pune Maternal Nutrition Study (PMNS) was established to prospectively study the relationship of maternal nutrition to fetal growth and later cardiometabolic risk in the offspring. High homocysteine and low vitamin B12 levels in pregnancy predicted lower birthweight and higher insulin resistance at 6 years in the offspring. B12 deficiency was widespread in this population, due to low dietary intake. We therefore commenced a community-based intervention study with the underlying hypothesis that vitamin B12 supplementation of adolescent members of the PMNS cohort will improve birth weight, B12 status, and reduce future diabetes risk, in their offspring. METHODS: The individually randomised controlled trial commenced in September 2012, with boys and girls randomized into 3 groups, to receive daily for at least 3 years or until the birth of their first child: 1) vitamin B12 2 μg; or 2) vitamin B12 2 μg plus multiple micronutrients (MMN) plus 20 g of milk powder or 3) placebo. Iron and folic acid is given to all participants. Compliance is assessed by monthly supplement counts. Adverse events are recorded using a standardised questionnaire. The primary outcome is cord blood B12 concentration; based on 180–200 pregnancies in the girls, the study has ~80% power to detect a 0.5 SD change in newborn B12, in the B12 supplementation groups compared with controls, at the 5% significance level. Primary analysis will be by intention to treat. DISCUSSION: Our study tests a primordial prevention strategy through an intergenerational intervention started pre-conceptionally in both boys and girls using physiological doses of micronutrients to improve immediate pregnancy-related and long-term cardio metabolic outcomes. The results will have significant public health implications in a setting with widespread B12 deficiency but relative folate sufficiency. The randomised controlled trial design allows us to be confident that our findings will be causally relevant. TRIAL REGISTRATION: ISRCTN 32921044, applied on 14/09/2012. CTRI 2012/12/003212, registered on 02/12/2012. Retrospectively registered.
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spelling pubmed-70508392020-03-09 The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial Kumaran, Kalyanaraman Yajnik, Pallavi Lubree, Himangi Joglekar, Charudatta Bhat, Dattatray Katre, Prachi Joshi, Suyog Ladkat, Rasika Fall, Caroline Yajnik, Chittaranjan BMC Nutr Study Protocol BACKGROUND: The Pune Maternal Nutrition Study (PMNS) was established to prospectively study the relationship of maternal nutrition to fetal growth and later cardiometabolic risk in the offspring. High homocysteine and low vitamin B12 levels in pregnancy predicted lower birthweight and higher insulin resistance at 6 years in the offspring. B12 deficiency was widespread in this population, due to low dietary intake. We therefore commenced a community-based intervention study with the underlying hypothesis that vitamin B12 supplementation of adolescent members of the PMNS cohort will improve birth weight, B12 status, and reduce future diabetes risk, in their offspring. METHODS: The individually randomised controlled trial commenced in September 2012, with boys and girls randomized into 3 groups, to receive daily for at least 3 years or until the birth of their first child: 1) vitamin B12 2 μg; or 2) vitamin B12 2 μg plus multiple micronutrients (MMN) plus 20 g of milk powder or 3) placebo. Iron and folic acid is given to all participants. Compliance is assessed by monthly supplement counts. Adverse events are recorded using a standardised questionnaire. The primary outcome is cord blood B12 concentration; based on 180–200 pregnancies in the girls, the study has ~80% power to detect a 0.5 SD change in newborn B12, in the B12 supplementation groups compared with controls, at the 5% significance level. Primary analysis will be by intention to treat. DISCUSSION: Our study tests a primordial prevention strategy through an intergenerational intervention started pre-conceptionally in both boys and girls using physiological doses of micronutrients to improve immediate pregnancy-related and long-term cardio metabolic outcomes. The results will have significant public health implications in a setting with widespread B12 deficiency but relative folate sufficiency. The randomised controlled trial design allows us to be confident that our findings will be causally relevant. TRIAL REGISTRATION: ISRCTN 32921044, applied on 14/09/2012. CTRI 2012/12/003212, registered on 02/12/2012. Retrospectively registered. BioMed Central 2017-05-08 /pmc/articles/PMC7050839/ /pubmed/32153821 http://dx.doi.org/10.1186/s40795-017-0143-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Kumaran, Kalyanaraman
Yajnik, Pallavi
Lubree, Himangi
Joglekar, Charudatta
Bhat, Dattatray
Katre, Prachi
Joshi, Suyog
Ladkat, Rasika
Fall, Caroline
Yajnik, Chittaranjan
The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title_full The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title_fullStr The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title_full_unstemmed The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title_short The Pune Rural Intervention in Young Adolescents (PRIYA) study: design and methods of a randomised controlled trial
title_sort pune rural intervention in young adolescents (priya) study: design and methods of a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050839/
https://www.ncbi.nlm.nih.gov/pubmed/32153821
http://dx.doi.org/10.1186/s40795-017-0143-5
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