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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 differe...

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Autores principales: 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., Kennedy, Stephen H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922239/
https://www.ncbi.nlm.nih.gov/pubmed/33646288
http://dx.doi.org/10.1001/jamapediatrics.2020.6087
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author 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.
Kennedy, Stephen H.
author_facet 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.
Kennedy, Stephen H.
author_sort Villar, Jose
collection PubMed
description 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.
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spelling pubmed-79222392021-03-19 Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study 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. Kennedy, Stephen H. JAMA Pediatr Original Investigation 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. American Medical Association 2021-03-01 2021-05 /pmc/articles/PMC7922239/ /pubmed/33646288 http://dx.doi.org/10.1001/jamapediatrics.2020.6087 Text en Copyright 2021 Villar J et al. JAMA Pediatrics. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
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.
Kennedy, Stephen H.
Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title_full Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title_fullStr Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title_full_unstemmed Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title_short Association Between Preterm-Birth Phenotypes and Differential Morbidity, Growth, and Neurodevelopment at Age 2 Years: Results From the INTERBIO-21st Newborn Study
title_sort association between preterm-birth phenotypes and differential morbidity, growth, and neurodevelopment at age 2 years: results from the interbio-21st newborn study
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922239/
https://www.ncbi.nlm.nih.gov/pubmed/33646288
http://dx.doi.org/10.1001/jamapediatrics.2020.6087
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