GROWTH-HORMONE, INSULIN-LIKE GROWTH-FACTOR-I AND PROLACTIN IN SMALL-FOR-GESTATIONAL-AGE NEONATES

Citation
A. Varvarigou et al., GROWTH-HORMONE, INSULIN-LIKE GROWTH-FACTOR-I AND PROLACTIN IN SMALL-FOR-GESTATIONAL-AGE NEONATES, Biology of the neonate, 65(2), 1994, pp. 94-102
Citations number
25
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
00063126
Volume
65
Issue
2
Year of publication
1994
Pages
94 - 102
Database
ISI
SICI code
0006-3126(1994)65:2<94:GIGAPI>2.0.ZU;2-V
Abstract
Growth hormone (hGH), insulin-like growth factor-I (IGF-I) and prolact in (PRL) were measured in the cord and venous blood of small for gesta tional age (SGA) neonates in order to evaluate their endocrine status during the first 3 days of life. Although there were SGA newborns with both high and normal levels of hGH, the mean (+/- SD) concentration o f hGH in the cord blood of the SGA neonates was 72.1 +/- 50.6 ng/ml, w hereas in the appropriate for gestational age (AGA) newborns it was 37 .0 +/- 23.5 (p = 0.001). The IGF-I in the cord blood of the SGA and th e AGA newborns was 194.2 +/- 174.8 ng/ml and 77.3 +/- 50.2, respective ly (p = 0.013). The PRL in the SGA and AGA newborns was 184.8 +/- 62.4 ng/ml and 126.8 +/- 60.5, respectively (p = 0.0005). On the 3rd day t he hGH in the SGA babies was 50.7 +/- 41.2, whereas in the AGA it was 24.3 +/- 12.3 (p = 0.034). On the same day the IGF-I was 133.9 +/- 120 .9 and 44.8 +/- 31.6, respectively (p > 0.05). Similarly, the PRL was 157.1 +/- 52.3 and 90.9 +/- 52.5, respectively (p = 0.0008). All neona tes with high hGH concentrations had low IGF-I levels, whereas of thos e with normal hGH half had high and half normal IGF-I levels. There wa s no difference in the hormone levels between symmetric and asymmetric intrauterine growth-retarded infants. The findings suggest that the S GA neonates are heterogeneous comprising three groups. The neonates wi th high hGH and low IGF-I may have resistance at the level of the hGH receptor or a defect in IGF-I synthesis, whereas those with normal hGH and high IGF-I may have a post-IGF-I receptor defect, with compensato ry increase in IGF-I synthesis independent of hGH control.