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Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway

Objective: To investigate the impact of fetal growth restriction (FGR) on hormonal regulation of post-natal growth and glucose metabolism [via insulin and growth hormone (GH)/Insulin-like Growth factor 1 (IGF1) axis pathways] in small for gestational age (SGA) neonates. Methods: We conducted a monoc...

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Autores principales: Motte-Signoret, Emmanuelle, Shankar-Aguilera, Shivani, Brailly-Tabard, Sylvie, Soreze, Yohan, Dell Orto, Valentina, Ben Ammar, Rafik, De Luca, Daniele, Boileau, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382944/
https://www.ncbi.nlm.nih.gov/pubmed/34447729
http://dx.doi.org/10.3389/fped.2021.711400
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author Motte-Signoret, Emmanuelle
Shankar-Aguilera, Shivani
Brailly-Tabard, Sylvie
Soreze, Yohan
Dell Orto, Valentina
Ben Ammar, Rafik
De Luca, Daniele
Boileau, Pascal
author_facet Motte-Signoret, Emmanuelle
Shankar-Aguilera, Shivani
Brailly-Tabard, Sylvie
Soreze, Yohan
Dell Orto, Valentina
Ben Ammar, Rafik
De Luca, Daniele
Boileau, Pascal
author_sort Motte-Signoret, Emmanuelle
collection PubMed
description Objective: To investigate the impact of fetal growth restriction (FGR) on hormonal regulation of post-natal growth and glucose metabolism [via insulin and growth hormone (GH)/Insulin-like Growth factor 1 (IGF1) axis pathways] in small for gestational age (SGA) neonates. Methods: We conducted a monocentric observational prospective comparative study on 73 singleton babies born with a weight inferior to 2,000 g. We analyzed auxological (weight, height and head circumference), and hormonal (GH, IGF1, and insulin plasma concentrations) data comparing SGA and appropriate for gestational age (AGA) neonates, between day 1 and 60. Results: One third (23/73) of the neonates were SGA. Twenty-five percent (18/73) required insulin for idiopathic hyperglycemia of prematurity and were smaller in weight and head circumference at discharge. In the SGA group compared with the AGA group, GH plasma concentrations were higher at day 3 (70.1 vs. 38.0 mIU/L) and IGF1 plasma concentrations were higher at day 10 (29.0 vs. 18.7 ng/ml). Conclusions: SGA neonates displayed resistance to GH and IGF1, concomitant to insulin resistance. This could partially explain the initial defective catch-up growth and, later in life, the higher prevalence of metabolic syndrome in this population.
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spelling pubmed-83829442021-08-25 Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway Motte-Signoret, Emmanuelle Shankar-Aguilera, Shivani Brailly-Tabard, Sylvie Soreze, Yohan Dell Orto, Valentina Ben Ammar, Rafik De Luca, Daniele Boileau, Pascal Front Pediatr Pediatrics Objective: To investigate the impact of fetal growth restriction (FGR) on hormonal regulation of post-natal growth and glucose metabolism [via insulin and growth hormone (GH)/Insulin-like Growth factor 1 (IGF1) axis pathways] in small for gestational age (SGA) neonates. Methods: We conducted a monocentric observational prospective comparative study on 73 singleton babies born with a weight inferior to 2,000 g. We analyzed auxological (weight, height and head circumference), and hormonal (GH, IGF1, and insulin plasma concentrations) data comparing SGA and appropriate for gestational age (AGA) neonates, between day 1 and 60. Results: One third (23/73) of the neonates were SGA. Twenty-five percent (18/73) required insulin for idiopathic hyperglycemia of prematurity and were smaller in weight and head circumference at discharge. In the SGA group compared with the AGA group, GH plasma concentrations were higher at day 3 (70.1 vs. 38.0 mIU/L) and IGF1 plasma concentrations were higher at day 10 (29.0 vs. 18.7 ng/ml). Conclusions: SGA neonates displayed resistance to GH and IGF1, concomitant to insulin resistance. This could partially explain the initial defective catch-up growth and, later in life, the higher prevalence of metabolic syndrome in this population. Frontiers Media S.A. 2021-08-10 /pmc/articles/PMC8382944/ /pubmed/34447729 http://dx.doi.org/10.3389/fped.2021.711400 Text en Copyright © 2021 Motte-Signoret, Shankar-Aguilera, Brailly-Tabard, Soreze, Dell Orto, Ben Ammar, De Luca and Boileau. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Motte-Signoret, Emmanuelle
Shankar-Aguilera, Shivani
Brailly-Tabard, Sylvie
Soreze, Yohan
Dell Orto, Valentina
Ben Ammar, Rafik
De Luca, Daniele
Boileau, Pascal
Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title_full Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title_fullStr Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title_full_unstemmed Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title_short Small for Gestational Age Preterm Neonates Exhibit Defective GH/IGF1 Signaling Pathway
title_sort small for gestational age preterm neonates exhibit defective gh/igf1 signaling pathway
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382944/
https://www.ncbi.nlm.nih.gov/pubmed/34447729
http://dx.doi.org/10.3389/fped.2021.711400
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