New Horizons in Short Children Born Small for Gestational Age

Children born small for gestational age (SGA) comprise a heterogeneous group due to the varied nature of the cause. Approximately 85–90% have catch-up growth within the first 4 postnatal years, while the remainder remain short. In later life, children born SGA have an increased risk to develop metab...

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Main Authors: Irène Netchine, Manouk van der Steen, Abel López-Bermejo, Ekaterina Koledova, Mohamad Maghnie
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.655931/full
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spelling doaj-a3210a8c17804f9b94f7b623c3178c112021-05-13T04:27:01ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602021-05-01910.3389/fped.2021.655931655931New Horizons in Short Children Born Small for Gestational AgeIrène Netchine0Manouk van der Steen1Abel López-Bermejo2Ekaterina Koledova3Mohamad Maghnie4Mohamad Maghnie5Sorbonne Université, INSERM, UMR_S938 Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, Paris, FranceDepartment of Paediatrics, Subdivision of Endocrinology, Erasmus University Medical Centre, Rotterdam, NetherlandsGirona Biomedical Research Institute, Dr. Josep Trueta Hospital, Girona, SpainGlobal Medical Affairs Department, Merck KGaA, Darmstadt, GermanyDepartment of Pediatrics, Institute for Research, Hospitalization and Health Care (IRCCS) Children's Hospital Giannina Gaslini, Genova, ItalyDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal, and Child Health, University of Genova, Genova, ItalyChildren born small for gestational age (SGA) comprise a heterogeneous group due to the varied nature of the cause. Approximately 85–90% have catch-up growth within the first 4 postnatal years, while the remainder remain short. In later life, children born SGA have an increased risk to develop metabolic abnormalities, including visceral adiposity, insulin resistance, and cardiovascular problems, and may have impaired pubertal onset and growth. The third “360° European Meeting on Growth and Endocrine Disorders” in Rome, Italy, in February 2018, funded by Merck KGaA, Germany, included a session that examined aspects of short children born SGA, with three presentations followed by a discussion period, on which this report is based. Children born SGA who remain short are eligible for GH treatment, which is an approved indication. GH treatment increases linear growth and can also improve some metabolic abnormalities. After stopping GH at near-adult height, metabolic parameters normalize, but pharmacological effects on lean body mass and fat mass are lost; continued monitoring of body composition and metabolic changes may be necessary. Guidelines have been published on diagnosis and management of children with Silver-Russell syndrome, who comprise a specific group of those born SGA; these children rarely have catch-up growth and GH treatment initiation as early as possible is recommended. Early and moderate pubertal growth spurt can occur in children born SGA, including those with Silver-Russell syndrome, and reduce adult height. Treatments that delay puberty, specifically metformin and gonadotropin releasing hormone analogs in combination with GH, have been proposed, but are used off-label, currently lack replication of data, and require further studies of efficacy and safety.https://www.frontiersin.org/articles/10.3389/fped.2021.655931/fullshort staturesmall for gestational ageSilver-Russell syndromeGH treatmentpubertymetabolic abnormalities
collection DOAJ
language English
format Article
sources DOAJ
author Irène Netchine
Manouk van der Steen
Abel López-Bermejo
Ekaterina Koledova
Mohamad Maghnie
Mohamad Maghnie
spellingShingle Irène Netchine
Manouk van der Steen
Abel López-Bermejo
Ekaterina Koledova
Mohamad Maghnie
Mohamad Maghnie
New Horizons in Short Children Born Small for Gestational Age
Frontiers in Pediatrics
short stature
small for gestational age
Silver-Russell syndrome
GH treatment
puberty
metabolic abnormalities
author_facet Irène Netchine
Manouk van der Steen
Abel López-Bermejo
Ekaterina Koledova
Mohamad Maghnie
Mohamad Maghnie
author_sort Irène Netchine
title New Horizons in Short Children Born Small for Gestational Age
title_short New Horizons in Short Children Born Small for Gestational Age
title_full New Horizons in Short Children Born Small for Gestational Age
title_fullStr New Horizons in Short Children Born Small for Gestational Age
title_full_unstemmed New Horizons in Short Children Born Small for Gestational Age
title_sort new horizons in short children born small for gestational age
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2021-05-01
description Children born small for gestational age (SGA) comprise a heterogeneous group due to the varied nature of the cause. Approximately 85–90% have catch-up growth within the first 4 postnatal years, while the remainder remain short. In later life, children born SGA have an increased risk to develop metabolic abnormalities, including visceral adiposity, insulin resistance, and cardiovascular problems, and may have impaired pubertal onset and growth. The third “360° European Meeting on Growth and Endocrine Disorders” in Rome, Italy, in February 2018, funded by Merck KGaA, Germany, included a session that examined aspects of short children born SGA, with three presentations followed by a discussion period, on which this report is based. Children born SGA who remain short are eligible for GH treatment, which is an approved indication. GH treatment increases linear growth and can also improve some metabolic abnormalities. After stopping GH at near-adult height, metabolic parameters normalize, but pharmacological effects on lean body mass and fat mass are lost; continued monitoring of body composition and metabolic changes may be necessary. Guidelines have been published on diagnosis and management of children with Silver-Russell syndrome, who comprise a specific group of those born SGA; these children rarely have catch-up growth and GH treatment initiation as early as possible is recommended. Early and moderate pubertal growth spurt can occur in children born SGA, including those with Silver-Russell syndrome, and reduce adult height. Treatments that delay puberty, specifically metformin and gonadotropin releasing hormone analogs in combination with GH, have been proposed, but are used off-label, currently lack replication of data, and require further studies of efficacy and safety.
topic short stature
small for gestational age
Silver-Russell syndrome
GH treatment
puberty
metabolic abnormalities
url https://www.frontiersin.org/articles/10.3389/fped.2021.655931/full
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