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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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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. |
format | Online Article Text |
id | pubmed-8382944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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