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Clin Endocrinol (Oxf) ; 72(2): 241-7, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19548955

RESUMEN

OBJECTIVE: Besides foetal or maternal disorders, placental dysfunction is a major cause of intrauterine growth restriction (IUGR). Although numerous macro- and histopathological changes have been described, little is known about the precise aetiology and the contribution of foetal/placental genes in this disorder. DESIGN: Placental tissues of 20 IUGR and control neonates were analysed by microarray technique. Four of the regulated genes with possible relevance in the pathogenesis of IUGR and its consequences were further studied in placentas of 27 IUGR and 35 control newborns. RESULTS: Elevated gene expression of leptin, corticotrophin-releasing hormone (CRH), and IGF-binding protein-1 (IGFBP-1) in IUGR placentas could be confirmed in the larger group by real-time PCR, whereas prolactin showed no significant difference. Accordingly, protein expression of leptin and IGFBP-1 depicted by Western blot was elevated in IUGR, prolactin was not different. Birthweight standard deviation score (SDS) correlated negatively to leptin, IGFBP-1, and CRH, whereas placental weight correlated only to IGFBP-1. Leptin correlated negatively to gestational age of IUGR patients and positively to placental score, a marker of severity of impaired foeto-placental circulation. CONCLUSIONS: As confirmed in a large group of IUGR and control samples, the up-regulated factors leptin, IGFBP-1, and CRH may serve as candidate genes for the prediction of subsequent metabolic consequences in IUGR newborns. These three factors may not only influence growth of the foetus, but might also interact with programming of its metabolic functions, which has to be determined in an ongoing study.


Asunto(s)
Retardo del Crecimiento Fetal/metabolismo , Análisis de Secuencia por Matrices de Oligonucleótidos , Placenta/metabolismo , Adulto , Western Blotting , Femenino , Retardo del Crecimiento Fetal/genética , Humanos , Recién Nacido , Leptina/metabolismo , Masculino , Embarazo , Radioinmunoensayo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Adulto Joven
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