Metabolic changes in plasma from the umbilical cord of small for gestational age babies and from a rat model of placental insufficiency. (16th November 2010)

• Record Type: Journal Article
• Authors: Horgan, RP; Broadhurst, DI; Dunn, WB; Walsh, SK; Brown, M; Kell, DB; Baker, PN; Kenny, LC
• Is Part Of: Archives of disease in childhood. Volume 95(2010)Supplement 1
• Page Start: Fa14
• Page End: Fa15
• Publication Date: 2010-11-16
• Subjects: Infants -- Diseases -- Periodicals; Newborn infants -- Diseases -- Periodicals; Fetus -- Diseases -- Periodicals; 618.920105
• DOI: 10.1136/adc.2010.189746.10
• Languages: English
• ISSNs: 1359-2998

Abstract

Abstract : Small for gestational age (SGA) can have lifelong consequences. Placental dysfunction is implicated in its pathophysiology. A reduced uterine perfusion pressure (RUPP) rat model can create an in vivo model of placental insufficiency. Metabolomics is the holistic study of the basic biochemistry within a biological system. The authors aimed to examine the metabolomic differences in (1) venous cord blood (VCB) plasma between SGA babies and normal controls and (2) plasma from the RUPP rat. Cord blood was collected from normally grown babies, and babies with confirmed SGA (n=7–8). Blood was also collected from RUPP, sham operated and control rats (n=7–9). All samples sets were analysed using Ultra Performance Liquid Chromatography/LTQ-Orbitrap Mass Spectrometry. In VCB, over 1700 metabolite features were detected, of which 900 (52%) showed significant difference between SGA and normally grown babies (p<0.05). Multivariate data analysis (Canonical Variates Analysis – CVA) showed that the metabolic profiles of normal and SGA samples were clearly different. Chemical identity of the metabolites will be elucidated fully but there was a preponderance of phospholipids and vitamin D derivatives. In rat plasma, there were 3825 metabolite features detected. 712 of these features had a p value <0.05. Multivariate data analysis showed that metabolite differences between normal and RUPP samples were highly correlated. Carnitine and phosphocholine metabolism were of notable interest. This study has shown metabolomic differences in VCB plasma between SGA babies and normal controls as well as in an animal model of placental insufficiency. Both studies may lead to a closer understanding of the aetiology of SGA.