Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]

Growth retardation (stunting, wasting and poor organ development) among children in low-income countries has major short and long-term health consequences yet very little is known about the nutritional and environmental influences on the key hormonal axes regulating child growth in these settings, n...

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Main Authors: Sophie E. Moore, Andrew M. Doel, Ken K. Ong, David B. Dunger, Nabeel A. Affara, Andrew M. Prentice, Robin M. Bernstein, HERO-G Working Group
Format: Article
Language:English
Published: F1000 Research Ltd 2020-02-01
Series:Gates Open Research
Online Access:https://gatesopenresearch.org/articles/4-25/v1
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spelling doaj-e62850f9d7b040ce85dfeae4810068f32021-03-08T14:20:03ZengF1000 Research LtdGates Open Research2572-47542020-02-01410.12688/gatesopenres.13101.114262Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]Sophie E. Moore0Andrew M. Doel1Ken K. Ong2David B. Dunger3Nabeel A. Affara4Andrew M. Prentice5Robin M. Bernstein6HERO-G Working GroupDepartment of Women and Children's Health, King's College London SE1 1UL, London, UKDepartment of Women and Children's Health, King's College London SE1 1UL, London, UKDepartment of Paediatrics, University of Cambridge Addenbrooke's Hospital Cambridge, Cambridge, UKDepartment of Paediatrics, University of Cambridge Addenbrooke's Hospital Cambridge, Cambridge, UKDepartment of Pathology, University of Cambridge, Cambridge, UKMRC Unit The Gambia, London School of Hygiene & Tropical Medicine, Fajara, The GambiaDepartment of Anthropology, University of Colorado, Boulder, CO, 80309, USAGrowth retardation (stunting, wasting and poor organ development) among children in low-income countries has major short and long-term health consequences yet very little is known about the nutritional and environmental influences on the key hormonal axes regulating child growth in these settings, nor the tempo and timing of faltering episodes. Here we describe the study protocol and provide a cohort description of the Hormonal and Epigenetic Regulators of Growth (HERO-G) study. This prospective cohort study from rural Gambia, West Africa, followed mothers and children longitudinally from pre-conception, through pregnancy, delivery, and to two years of child age A total of 251 eligible mother-infant pairs were recruited into the HERO-G study, with 206 (82%) followed up until two years of age. Women were seen at scheduled antenatal appointments at 20, 28 and 36 weeks of gestation, and at delivery, where possible. Between one week and 12 months of age, infants were visited every second day for collection of detailed anthropometry and morbidity data. Infants identified as about to enter a growth faltering episode at these visits entered a more detailed 20-day protocol, with the collection of dried blood spots, anthropometry and body composition. All infants were seen for scheduled clinic visits at 3, 6, 9, 12, 18 and 24 months of age for clinical examination and venous blood draw. Data from the HERO-G study is being used to explore three major mechanistic pathways influencing growth: 1) genome-wide investigations for signatures of epigenetic effects on any loci that might affect growth; 2) frequent anthropometric measurement coupled with non-invasive monitoring for rapid identification and interrogation of real-time faltering patterns and aetiology; 3) focused measurement of hormones and cytokines that act together in an integrated manner, both in utero and after birth, to coordinate patterns of growth with immune activation, inflammation, and nutritional status.https://gatesopenresearch.org/articles/4-25/v1
collection DOAJ
language English
format Article
sources DOAJ
author Sophie E. Moore
Andrew M. Doel
Ken K. Ong
David B. Dunger
Nabeel A. Affara
Andrew M. Prentice
Robin M. Bernstein
HERO-G Working Group
spellingShingle Sophie E. Moore
Andrew M. Doel
Ken K. Ong
David B. Dunger
Nabeel A. Affara
Andrew M. Prentice
Robin M. Bernstein
HERO-G Working Group
Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
Gates Open Research
author_facet Sophie E. Moore
Andrew M. Doel
Ken K. Ong
David B. Dunger
Nabeel A. Affara
Andrew M. Prentice
Robin M. Bernstein
HERO-G Working Group
author_sort Sophie E. Moore
title Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
title_short Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
title_full Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
title_fullStr Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
title_full_unstemmed Identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural African fetuses and infants: Project protocol and cohort description [version 1; peer review: 2 approved]
title_sort identification of nutritionally modifiable hormonal and epigenetic drivers of positive and negative growth deviance in rural african fetuses and infants: project protocol and cohort description [version 1; peer review: 2 approved]
publisher F1000 Research Ltd
series Gates Open Research
issn 2572-4754
publishDate 2020-02-01
description Growth retardation (stunting, wasting and poor organ development) among children in low-income countries has major short and long-term health consequences yet very little is known about the nutritional and environmental influences on the key hormonal axes regulating child growth in these settings, nor the tempo and timing of faltering episodes. Here we describe the study protocol and provide a cohort description of the Hormonal and Epigenetic Regulators of Growth (HERO-G) study. This prospective cohort study from rural Gambia, West Africa, followed mothers and children longitudinally from pre-conception, through pregnancy, delivery, and to two years of child age A total of 251 eligible mother-infant pairs were recruited into the HERO-G study, with 206 (82%) followed up until two years of age. Women were seen at scheduled antenatal appointments at 20, 28 and 36 weeks of gestation, and at delivery, where possible. Between one week and 12 months of age, infants were visited every second day for collection of detailed anthropometry and morbidity data. Infants identified as about to enter a growth faltering episode at these visits entered a more detailed 20-day protocol, with the collection of dried blood spots, anthropometry and body composition. All infants were seen for scheduled clinic visits at 3, 6, 9, 12, 18 and 24 months of age for clinical examination and venous blood draw. Data from the HERO-G study is being used to explore three major mechanistic pathways influencing growth: 1) genome-wide investigations for signatures of epigenetic effects on any loci that might affect growth; 2) frequent anthropometric measurement coupled with non-invasive monitoring for rapid identification and interrogation of real-time faltering patterns and aetiology; 3) focused measurement of hormones and cytokines that act together in an integrated manner, both in utero and after birth, to coordinate patterns of growth with immune activation, inflammation, and nutritional status.
url https://gatesopenresearch.org/articles/4-25/v1
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