Eur J Endocrinol
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DOI: 10.1530/EJE-07-0286
European Journal of Endocrinology, Vol 157, Issue 5, 605-612
Copyright © 2007 by European Society of Endocrinology
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CLINICAL STUDIES

Impact of fetal growth restriction on body composition and hormonal status at birth in infants of small and appropriate weight for gestational age

R Verkauskiene, J Beltrand, O Claris1, D Chevenne2, S Deghmoun, S Dorgeret3, M Alison3, P Gaucherand4, O Sibony5 and C Lévy-Marchal

INSERM, Unité de recherche U690, Hôpital Robert Debré, 48, bd Serurier, 75019 Paris, France
1 Service de Néonatologie, Hôpital Edouard Herriot, Lyon, France
2 Service de biochimie et d'hormonologie,
3 Service d'Imagerie Médicale, Hôpital Robert Debré, Paris, France
4 Service de Chirurgie Gynecologie-Obstetrique, Hôpital Eduard Herriot, Lyon, France
5 Service de Chirurgie Gynecologie-Obstetrique, Hôpital Robert Debré, Paris, France

(Correspondence should be addressed to R Verkauskiene Email: rasa.verkauskiene{at}yahoo.com)

Background: Fetal growth restriction (FGR) has been related to several health risks, which have been generally identified in small-for-gestational age (SGA) individuals.

Objective: To evaluate the impact of FGR on body composition and hormonal status in infants born either small- or appropriate-for-gestational age (AGA).

Methods: Fetal growth was assessed by ultrasound every 4 weeks from mid-gestation to birth in 248 high-risk pregnancies for SGA. Fetal growth velocity was calculated as change in the estimated fetal weight percentiles and FGR defined as its reduction by more than 20 percentiles from 22 gestational weeks to birth. Impact of FGR on body composition, cord insulin, IGF-I, IGF binding protein-3 (IGFBP-3), and cortisol concentrations was assessed in SGA and AGA newborns.

Results: Growth-retarded AGA infants showed significantly reduced birth weight, ponderal index, percentage of fat mass, and bone mineral density when compared with AGA newborns with stable intrauterine growth. Cord IGF-I and IGFBP-3 concentrations were significantly decreased in growth-retarded infants in both SGA and AGA groups. Cord insulin concentration was significantly lower and cord cortisol significantly higher in AGA infants with FGR versus AGA newborns with stable intrauterine growth.

After adjustment for gestational age and gender, birth weight was directly related to fetal growth velocity and cord IGF-I concentration. The variation in infant's adiposity was best explained by fetal growth velocity and cord insulin concentration.

Conclusions: FGR affects body composition and hormonal parameters in newborns with birth weight within the normal range, suggesting these individuals could be at similar metabolic risks as SGA.




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