IGF-I AND IGF-BINDING PROTEIN-1 ARE RELATED TO CORTISOL IN HUMAN CORD-BLOOD

Citation
S. Cianfarani et al., IGF-I AND IGF-BINDING PROTEIN-1 ARE RELATED TO CORTISOL IN HUMAN CORD-BLOOD, European journal of endocrinology, 138(5), 1998, pp. 524-529
Citations number
31
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
08044643
Volume
138
Issue
5
Year of publication
1998
Pages
524 - 529
Database
ISI
SICI code
0804-4643(1998)138:5<524:IAIPAR>2.0.ZU;2-#
Abstract
Objective: To assess cortisol concentrations in cord blood and investi gate their relationships with the IGF system. Study design: Fifteen ne wborns with birth weight appropriate for gestational age (AGA) and 30 children with intrauterine growth retardation (IUGR) were studied. Ser um samples were collected from umbilical cord blood and cortisol, IGF- T and IGF-binding proteins (IGFBPs)-1 and -3 were measured. IUGR infan ts were followed up for 3 months with repeated measurements of weight, supine length and knee-heel length (by knemometry). Results: IUGR new borns showed significantly greater concentrations of IGFBP-1 (P < 0.00 01) and lower concentrations of IGF-I (P < 0.0001) and IGFBP-3 (P < 0. 0001) than did controls, In AGA children, cortisol correlated inversel y with IGF-I(r = -0.75, P < 0.002) and directly with IGFBP-1 (r = 0.52 , P < 0.05), whereas no correlation between cortisol and IGF system-re lated variables was observed in IUGR. Finally, in IUGR children an inv erse correlation was found between length gain in the first trimester of life and cortisol concentrations at birth (r = -0.54, P < 0.005). C onclusions: Cortisol might be a physiological regulator of fetal growt h, at least in the last: part of pregnancy, by modulating IGF-I and IG FBP-1 release under conditions of fetal stress. In IUGR children, a re arrangement of this growth control mechanism seems to occur. The close inverse relationship of cortisol with linear growth, if confirmed by large-scale studies, suggests cord blood cortisol to be potentially pr edictive of early postnatal catch-up growth in IUGR infants.