Publication:
Association between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results from the INTERBIO-21st Newborn Study

dc.contributor.authorJose Villaren_US
dc.contributor.authorMaría C. Restrepo-Méndezen_US
dc.contributor.authorRose McGreadyen_US
dc.contributor.authorFernando C. Barrosen_US
dc.contributor.authorCesar G. Victoraen_US
dc.contributor.authorShama Munimen_US
dc.contributor.authorAris T. Papageorghiouen_US
dc.contributor.authorRoseline Ochiengen_US
dc.contributor.authorRachel Craiken_US
dc.contributor.authorHellen C. Barsosioen_US
dc.contributor.authorJames A. Berkleyen_US
dc.contributor.authorMaria Carvalhoen_US
dc.contributor.authorMichelle Fernandesen_US
dc.contributor.authorLeila Cheikh Ismailen_US
dc.contributor.authorAnn Lamberten_US
dc.contributor.authorShane A. Norrisen_US
dc.contributor.authorEric O. Ohumaen_US
dc.contributor.authorAlan Steinen_US
dc.contributor.authorChrystelle O.O. Tshivuila-Matalaen_US
dc.contributor.authorKrina T. Zondervanen_US
dc.contributor.authorAdele Winseyen_US
dc.contributor.authorFrancois Nostenen_US
dc.contributor.authorRicardo Uauyen_US
dc.contributor.authorZulfiqar A. Bhuttaen_US
dc.contributor.authorStephen H. Kennedyen_US
dc.contributor.otherFaculty of Tropical Medicine, Mahidol Universityen_US
dc.contributor.otherThe Wellcome Centre for Human Geneticsen_US
dc.contributor.otherUniversity of Sharjahen_US
dc.contributor.otherWellcome Trust Research Laboratories Nairobien_US
dc.contributor.otherAga Khan Hospital Nairobien_US
dc.contributor.otherThe Aga Khan Universityen_US
dc.contributor.otherLondon School of Hygiene & Tropical Medicineen_US
dc.contributor.otherHospital for Sick Children University of Torontoen_US
dc.contributor.otherGreen Templeton Collegeen_US
dc.contributor.otherUniversity of Oxforden_US
dc.contributor.otherUniversity of Southampton, Faculty of Medicineen_US
dc.contributor.otherUniversidade Catolica de Pelotasen_US
dc.contributor.otherLiverpool School of Tropical Medicineen_US
dc.contributor.otherThe World Bank Groupen_US
dc.contributor.otherUniversity of the Witwatersrand, Johannesburgen_US
dc.contributor.otherUniversidade Federal de Pelotasen_US
dc.contributor.otherWits School of Public Healthen_US
dc.contributor.otherNuffield Department of Medicineen_US
dc.contributor.otherUniversity of Oxford Medical Sciences Divisionen_US
dc.date.accessioned2022-08-04T09:26:01Z
dc.date.available2022-08-04T09:26:01Z
dc.date.issued2021-05-01en_US
dc.description.abstractImportance: 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..en_US
dc.identifier.citationJAMA Pediatrics. Vol.175, No.5 (2021), 483-493en_US
dc.identifier.doi10.1001/jamapediatrics.2020.6087en_US
dc.identifier.issn21686211en_US
dc.identifier.issn21686203en_US
dc.identifier.other2-s2.0-85101738023en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/78264
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85101738023&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAssociation between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results from the INTERBIO-21st Newborn Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85101738023&origin=inwarden_US

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