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Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21st Newborn Case-Control Study protocol

Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21st Newborn Case-Control Study protocol
Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21st Newborn Case-Control Study protocol
Background: INTERBIO-21st is Phase II of the INTERGROWTH-21st Project, the population-based, research initiative involving nearly 70,000 mothers and babies worldwide coordinated by Oxford University and performed by a multidisciplinary network of more than 400 healthcare professionals and scientists from 35 institutions in 21 countries worldwide. Phase I, conducted 2008-2015, consisted of nine complementary studies designed to describe optimal human growth and neurodevelopment, based conceptually on the WHO prescriptive approach. The studies generated a set of international standards for monitoring growth and neurodevelopment, which complement the existing WHO Child Growth Standards. Phase II aims to improve the functional classification of the highly heterogenous preterm birth and fetal growth restriction syndromes through a better understanding of how environmental exposures, clinical conditions and nutrition influence patterns of human growth from conception to childhood, as well as specific neurodevelopmental domains and associated behaviors at 2 years of age. Methods: In the INTERBIO-21st Newborn Case-Control Study, a major component of Phase II, our objective is to investigate the mechanisms potentially responsible for preterm birth and small for gestational age and their interactions, using deep phenotyping of clinical, growth and epidemiological data and associated nutritional, biochemical, omic and histological profiles. Here we describe the study sites, population characteristics, study design, methodology and standardization procedures for the collection of longitudinal clinical data and biological samples (maternal blood, umbilical cord blood, placental tissue, maternal feces and infant buccal swabs) for the study that was conducted between 2012 and 2018 in Brazil, Kenya, Pakistan, South Africa, Thailand and the UK. Discussion: Our study provides a unique resource for the planned analyses given the range of potentially disadvantageous exposures (including poor nutrition, pregnancy complications and infections) in geographically diverse populations worldwide. The study should enhance current medical knowledge and provide new insights into environmental influences on human growth and neurodevelopment.
2572-4754
Kennedy, Stephen
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Victora, Cesar G.
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Craik, Rachel
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Ash, Stephen
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Barros, Fernando C.
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Barsosio, Hellen C.
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Berkley, James A.
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Carvalho, Maria
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Fernandes, Michelle
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Cheikh Ismail, Leila
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Lambert, Ann
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Lindgren, Cecilia M.
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McGready, Rose
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Munim, Shama
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Nellaker, Christoffer
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Noble, Julia Alison
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Norris, Shane A
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Nosten, Francois
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Ohuma, Eric O.
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Papageorghiou, Aris T.
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Stein, Alan
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Stones, William
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Tshivuila-Matala, Chrystelle O.O.
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Urias, Eleonora Staines
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Vatish, Manu
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Wulff, Katharina
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Zainab, Ghulam
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Zondervan, Krina T
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Uauy, Ricardo
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Bhutta, Zulfiqar A.
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Villar, Jose
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Kennedy, Stephen
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Victora, Cesar G.
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Craik, Rachel
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Ash, Stephen
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Barros, Fernando C.
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Barsosio, Hellen C.
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Berkley, James A.
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Carvalho, Maria
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Fernandes, Michelle
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Cheikh Ismail, Leila
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Lambert, Ann
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Lindgren, Cecilia M.
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McGready, Rose
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Munim, Shama
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Nellaker, Christoffer
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Noble, Julia Alison
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Norris, Shane A
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Nosten, Francois
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Ohuma, Eric O.
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Papageorghiou, Aris T.
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Stein, Alan
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Stones, William
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Tshivuila-Matala, Chrystelle O.O.
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Urias, Eleonora Staines
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Vatish, Manu
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Wulff, Katharina
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Zainab, Ghulam
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Zondervan, Krina T
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Uauy, Ricardo
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Bhutta, Zulfiqar A.
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Villar, Jose
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Kennedy, Stephen, Victora, Cesar G., Craik, Rachel, Ash, Stephen, Barros, Fernando C., Barsosio, Hellen C., Berkley, James A., Carvalho, Maria, Fernandes, Michelle, Cheikh Ismail, Leila, Lambert, Ann, Lindgren, Cecilia M., McGready, Rose, Munim, Shama, Nellaker, Christoffer, Noble, Julia Alison, Norris, Shane A, Nosten, Francois, Ohuma, Eric O., Papageorghiou, Aris T., Stein, Alan, Stones, William, Tshivuila-Matala, Chrystelle O.O., Urias, Eleonora Staines, Vatish, Manu, Wulff, Katharina, Zainab, Ghulam, Zondervan, Krina T, Uauy, Ricardo, Bhutta, Zulfiqar A. and Villar, Jose (2019) Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21st Newborn Case-Control Study protocol. Gates Open Research, 2 (49). (doi:10.12688/gatesopenres.12869.2).

Record type: Article

Abstract

Background: INTERBIO-21st is Phase II of the INTERGROWTH-21st Project, the population-based, research initiative involving nearly 70,000 mothers and babies worldwide coordinated by Oxford University and performed by a multidisciplinary network of more than 400 healthcare professionals and scientists from 35 institutions in 21 countries worldwide. Phase I, conducted 2008-2015, consisted of nine complementary studies designed to describe optimal human growth and neurodevelopment, based conceptually on the WHO prescriptive approach. The studies generated a set of international standards for monitoring growth and neurodevelopment, which complement the existing WHO Child Growth Standards. Phase II aims to improve the functional classification of the highly heterogenous preterm birth and fetal growth restriction syndromes through a better understanding of how environmental exposures, clinical conditions and nutrition influence patterns of human growth from conception to childhood, as well as specific neurodevelopmental domains and associated behaviors at 2 years of age. Methods: In the INTERBIO-21st Newborn Case-Control Study, a major component of Phase II, our objective is to investigate the mechanisms potentially responsible for preterm birth and small for gestational age and their interactions, using deep phenotyping of clinical, growth and epidemiological data and associated nutritional, biochemical, omic and histological profiles. Here we describe the study sites, population characteristics, study design, methodology and standardization procedures for the collection of longitudinal clinical data and biological samples (maternal blood, umbilical cord blood, placental tissue, maternal feces and infant buccal swabs) for the study that was conducted between 2012 and 2018 in Brazil, Kenya, Pakistan, South Africa, Thailand and the UK. Discussion: Our study provides a unique resource for the planned analyses given the range of potentially disadvantageous exposures (including poor nutrition, pregnancy complications and infections) in geographically diverse populations worldwide. The study should enhance current medical knowledge and provide new insights into environmental influences on human growth and neurodevelopment.

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More information

Published date: 5 February 2019
Additional Information: © 2019 Kennedy SH et al.

Identifiers

Local EPrints ID: 468264
URI: http://eprints.soton.ac.uk/id/eprint/468264
ISSN: 2572-4754
PURE UUID: 3b05d143-0fbe-43c5-bef2-bf5a8b2cc580
ORCID for Michelle Fernandes: ORCID iD orcid.org/0000-0002-0051-3389

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Date deposited: 09 Aug 2022 16:37
Last modified: 17 Mar 2024 04:10

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Contributors

Author: Stephen Kennedy
Author: Cesar G. Victora
Author: Rachel Craik
Author: Stephen Ash
Author: Fernando C. Barros
Author: Hellen C. Barsosio
Author: James A. Berkley
Author: Maria Carvalho
Author: Michelle Fernandes ORCID iD
Author: Leila Cheikh Ismail
Author: Ann Lambert
Author: Cecilia M. Lindgren
Author: Rose McGready
Author: Shama Munim
Author: Christoffer Nellaker
Author: Julia Alison Noble
Author: Shane A Norris
Author: Francois Nosten
Author: Eric O. Ohuma
Author: Aris T. Papageorghiou
Author: Alan Stein
Author: William Stones
Author: Chrystelle O.O. Tshivuila-Matala
Author: Eleonora Staines Urias
Author: Manu Vatish
Author: Katharina Wulff
Author: Ghulam Zainab
Author: Krina T Zondervan
Author: Ricardo Uauy
Author: Zulfiqar A. Bhutta
Author: Jose Villar

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