Association between preterm-birth phenotypes and differential morbidity, growth, and neurodevelopment at age 2 years: results from the INTERBIO-21st Newborn Study
Association between preterm-birth phenotypes and differential morbidity, growth, and neurodevelopment at age 2 years: results from the INTERBIO-21st Newborn Study
Importance: the etiologic complexities of preterm birth remain inadequately understood, which may impede the development of better preventative and treatment measures.
Objective: to examine the association between specific preterm-birth phenotypes and clinical, growth, and neurodevelopmental differences among preterm newborns compared with term newborns up to age 2 years.
Design, Setting, and Participants: the INTERBIO-21st study included a cohort of preterm and term newborn singletons enrolled between March 2012 and June 2018 from maternity hospitals in 6 countries worldwide who were followed up from birth to age 2 years. All pregnancies were dated by ultrasonography. Data were analyzed from November 2019 to October 2020.
Exposures/Interventions: preterm-birth phenotypes.
Main Outcomes and Measures: infant size, health, nutrition, and World Health Organization motor development milestones assessed at ages 1 and 2 years; neurodevelopment evaluated at age 2 years using the INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) tool.
Results: a total of 6529 infants (3312 boys [50.7%]) were included in the analysis. Of those, 1381 were preterm births (mean [SD] gestational age at birth, 34.4 [0.1] weeks; 5148 were term births (mean [SD] gestational age at birth, 39.4 [0] weeks). Among 1381 preterm newborns, 8 phenotypes were identified: no main maternal, fetal, or placental condition detected (485 infants [35.1%]); infections (289 infants [20.9%]); preeclampsia (162 infants [11.7%]); fetal distress (131 infants [9.5%]); intrauterine growth restriction (110 infants [8.0%]); severe maternal disease (85 infants [6.2%]); bleeding (71 infants [5.1%]); and congenital anomaly (48 infants [3.5%]). For all phenotypes, a previous preterm birth was a risk factor for recurrence. Each phenotype displayed differences in neonatal morbidity and infant outcomes. For example, infants with the no main condition detected phenotype had low neonatal morbidity but increased morbidity and hospitalization incidence at age 1 year (odds ratio [OR], 2.2; 95% CI, 1.8-2.7). Compared with term newborns, the highest risk of scoring lower than the 10th centile of INTER-NDA normative values was observed in the fine motor development domain among newborns with the fetal distress (OR, 10.6; 95% CI, 5.1-22.2) phenotype.
Conclusions and Relevance: results of this study suggest that phenotypic classification may provide a better understanding of the etiologic factors and mechanisms associated with preterm birth than continuing to consider it an exclusively time-based entity.
483-493
Villar, Jose
316f758c-97b0-42a3-9b04-b7ead75181ee
Restrepo-Méndez, María C
f3e6f966-f029-4b0e-ba9b-d417a9dc4b86
McGready, Rose
901b40d0-a81c-4d92-bebf-7573eb8df859
Barros, Fernando C
2045a98e-ac82-4ce3-9f93-1c302da3492a
Victora, Cesar G
14b4c4b5-c082-4ee8-9c07-4e575af03ebf
Munim, Shama
4814acaa-0c90-4407-89ad-2beb71fe2d09
Papageorghiou, Aris T
48974657-d399-4f7f-8b8b-5b9174b8fefa
Ochieng, Roseline
eba8d4c0-7536-4eab-942b-9fe6deb5d9b0
Craik, Rachel
fbbea8df-8123-4c97-adda-8f70be3de5f8
Barsosio, Hellen C
c5c5984c-a4b0-4bab-a8bc-ec4df12bcf4d
Berkley, James A
faa94c98-0c5e-46ce-957f-2d1913c126b9
Carvalho, Maria
c50509dc-e16f-46ce-802d-294ecd4794f1
Fernandes, Michelle
16d62e60-ae8e-455f-88d3-88e778253b4a
Cheikh Ismail, Leila
fe340f86-4e83-4fb3-9b11-d3fdb034f64d
Lambert, Ann
b87eb4cd-696f-49d2-951f-5157fc46f5e1
Norris, Shane A
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Ohuma, Eric O
dcb8336d-f211-42d6-8a41-a7eb43b70763
Stein, Alan
ba341b04-0b18-411a-9926-44182a628a1d
Tshivuila-Matala, Chrystelle O O
5df4a9ba-9c91-475d-9c30-25aff4e0800b
Zondervan, Krina T
4d41922f-42a2-4552-93b3-2155feb00ded
Winsey, Adele
3e007cd5-c5b4-4e62-bfe5-2576b5f017cd
Nosten, Francois
5ec6a4aa-625e-4e75-9349-756f38830d2f
Uauy, Ricardo
60dfd38e-ef39-48df-82bc-459f19fe5e22
Bhutta, Zulfiqar A
009c4f8b-3ae6-4a0d-a666-9997d49dd292
Kennedy, Stephen H
a5b20ce3-8641-41a8-9d79-586948550796
Villar, Jose
316f758c-97b0-42a3-9b04-b7ead75181ee
Restrepo-Méndez, María C
f3e6f966-f029-4b0e-ba9b-d417a9dc4b86
McGready, Rose
901b40d0-a81c-4d92-bebf-7573eb8df859
Barros, Fernando C
2045a98e-ac82-4ce3-9f93-1c302da3492a
Victora, Cesar G
14b4c4b5-c082-4ee8-9c07-4e575af03ebf
Munim, Shama
4814acaa-0c90-4407-89ad-2beb71fe2d09
Papageorghiou, Aris T
48974657-d399-4f7f-8b8b-5b9174b8fefa
Ochieng, Roseline
eba8d4c0-7536-4eab-942b-9fe6deb5d9b0
Craik, Rachel
fbbea8df-8123-4c97-adda-8f70be3de5f8
Barsosio, Hellen C
c5c5984c-a4b0-4bab-a8bc-ec4df12bcf4d
Berkley, James A
faa94c98-0c5e-46ce-957f-2d1913c126b9
Carvalho, Maria
c50509dc-e16f-46ce-802d-294ecd4794f1
Fernandes, Michelle
16d62e60-ae8e-455f-88d3-88e778253b4a
Cheikh Ismail, Leila
fe340f86-4e83-4fb3-9b11-d3fdb034f64d
Lambert, Ann
b87eb4cd-696f-49d2-951f-5157fc46f5e1
Norris, Shane A
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Ohuma, Eric O
dcb8336d-f211-42d6-8a41-a7eb43b70763
Stein, Alan
ba341b04-0b18-411a-9926-44182a628a1d
Tshivuila-Matala, Chrystelle O O
5df4a9ba-9c91-475d-9c30-25aff4e0800b
Zondervan, Krina T
4d41922f-42a2-4552-93b3-2155feb00ded
Winsey, Adele
3e007cd5-c5b4-4e62-bfe5-2576b5f017cd
Nosten, Francois
5ec6a4aa-625e-4e75-9349-756f38830d2f
Uauy, Ricardo
60dfd38e-ef39-48df-82bc-459f19fe5e22
Bhutta, Zulfiqar A
009c4f8b-3ae6-4a0d-a666-9997d49dd292
Kennedy, Stephen H
a5b20ce3-8641-41a8-9d79-586948550796
Villar, Jose, Restrepo-Méndez, María C, McGready, Rose, Barros, Fernando C, Victora, Cesar G, Munim, Shama, Papageorghiou, Aris T, Ochieng, Roseline, Craik, Rachel, Barsosio, Hellen C, Berkley, James A, Carvalho, Maria, Fernandes, Michelle, Cheikh Ismail, Leila, Lambert, Ann, Norris, Shane A, Ohuma, Eric O, Stein, Alan, Tshivuila-Matala, Chrystelle O O, Zondervan, Krina T, Winsey, Adele, Nosten, Francois, Uauy, Ricardo, Bhutta, Zulfiqar A and Kennedy, Stephen H
(2021)
Association between preterm-birth phenotypes and differential morbidity, growth, and neurodevelopment at age 2 years: results from the INTERBIO-21st Newborn Study.
JAMA Pediatrics, 175 (5), .
(doi:10.1001/jamapediatrics.2020.6087).
Abstract
Importance: the etiologic complexities of preterm birth remain inadequately understood, which may impede the development of better preventative and treatment measures.
Objective: to examine the association between specific preterm-birth phenotypes and clinical, growth, and neurodevelopmental differences among preterm newborns compared with term newborns up to age 2 years.
Design, Setting, and Participants: the INTERBIO-21st study included a cohort of preterm and term newborn singletons enrolled between March 2012 and June 2018 from maternity hospitals in 6 countries worldwide who were followed up from birth to age 2 years. All pregnancies were dated by ultrasonography. Data were analyzed from November 2019 to October 2020.
Exposures/Interventions: preterm-birth phenotypes.
Main Outcomes and Measures: infant size, health, nutrition, and World Health Organization motor development milestones assessed at ages 1 and 2 years; neurodevelopment evaluated at age 2 years using the INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) tool.
Results: a total of 6529 infants (3312 boys [50.7%]) were included in the analysis. Of those, 1381 were preterm births (mean [SD] gestational age at birth, 34.4 [0.1] weeks; 5148 were term births (mean [SD] gestational age at birth, 39.4 [0] weeks). Among 1381 preterm newborns, 8 phenotypes were identified: no main maternal, fetal, or placental condition detected (485 infants [35.1%]); infections (289 infants [20.9%]); preeclampsia (162 infants [11.7%]); fetal distress (131 infants [9.5%]); intrauterine growth restriction (110 infants [8.0%]); severe maternal disease (85 infants [6.2%]); bleeding (71 infants [5.1%]); and congenital anomaly (48 infants [3.5%]). For all phenotypes, a previous preterm birth was a risk factor for recurrence. Each phenotype displayed differences in neonatal morbidity and infant outcomes. For example, infants with the no main condition detected phenotype had low neonatal morbidity but increased morbidity and hospitalization incidence at age 1 year (odds ratio [OR], 2.2; 95% CI, 1.8-2.7). Compared with term newborns, the highest risk of scoring lower than the 10th centile of INTER-NDA normative values was observed in the fine motor development domain among newborns with the fetal distress (OR, 10.6; 95% CI, 5.1-22.2) phenotype.
Conclusions and Relevance: results of this study suggest that phenotypic classification may provide a better understanding of the etiologic factors and mechanisms associated with preterm birth than continuing to consider it an exclusively time-based entity.
Text
jamapediatrics_villar_2021_oi_200098_1619729262.96142
- Version of Record
More information
Accepted/In Press date: 14 October 2020
e-pub ahead of print date: 21 March 2021
Additional Information:
Funding Information:
Funding/Support: This study was supported by grant 49038 from the Bill and Melinda Gates Foundation to the University of Oxford.
Funding Information:
receiving grants from the Bill and Melinda Gates Foundation during the conduct of the study. Dr Victora reported receiving grants from the Bill and Melinda Gates Foundation during the conduct of the study. Dr Papageorghiou reported receiving grants from the Bill and Melinda Gates Foundation during the conduct of the study and grants from the Bill and Melinda Gates Foundation, the European Research Council, and the National Institute of Health Research; personal fees from the British Journal of Obstetrics and Gynaecology, Intelligent Ultrasound, the National Health Service of the United Kingdom, and Ultrasound Diagnostic Services; being a cofounder, shareholder, and senior advisor of Intelligent Ultrasound; being a paid scientific advisor for Oxford University Innovation; and being a deputy editor-in-chief of the British Journal of Obstetrics and Gynaecology outside the submitted work. Dr Ochieng reported receiving grants from the University of Oxford during the conduct of the study. Dr Lambert reported receiving grants from the Bill and Melinda Gates Foundation during the conduct of the study. Dr Tshivuila-Matala reported receiving a scholarship and stipend for living expenses from the Rhodes Trust during the conduct of the study. Dr Winsey reported receiving grants from the Nuffield Department of Women’s and Reproductive Health during the conduct of the study. No other disclosures were reported.
Publisher Copyright:
© 2021 American Medical Association. All rights reserved.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Identifiers
Local EPrints ID: 452303
URI: http://eprints.soton.ac.uk/id/eprint/452303
ISSN: 2168-6203
PURE UUID: b94f333b-a495-4d0d-9bc1-baac92b391e3
Catalogue record
Date deposited: 06 Dec 2021 17:35
Last modified: 10 Oct 2024 02:02
Export record
Altmetrics
Contributors
Author:
Jose Villar
Author:
María C Restrepo-Méndez
Author:
Rose McGready
Author:
Fernando C Barros
Author:
Cesar G Victora
Author:
Shama Munim
Author:
Aris T Papageorghiou
Author:
Roseline Ochieng
Author:
Rachel Craik
Author:
Hellen C Barsosio
Author:
James A Berkley
Author:
Maria Carvalho
Author:
Michelle Fernandes
Author:
Leila Cheikh Ismail
Author:
Ann Lambert
Author:
Eric O Ohuma
Author:
Alan Stein
Author:
Chrystelle O O Tshivuila-Matala
Author:
Krina T Zondervan
Author:
Adele Winsey
Author:
Francois Nosten
Author:
Ricardo Uauy
Author:
Zulfiqar A Bhutta
Author:
Stephen H Kennedy
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics