Altered proteome profiles in maternal plasma in pregnancies with fetal growth restriction |
| |
Authors: | Madhulika B. Gupta Maxim D. Seferovic Suya Liu Robert J. Gratton Amanda Doherty-Kirby Gilles A. Lajoie Victor K. M. Han |
| |
Affiliation: | (1) Department of Pediatrics, University of Western Ontario, 800 Commissioners Road E., N6C2V5 London, ON, Canada;(2) Department of Biochemistry, University of Western Ontario, London, Canada;(3) Department of Obstetrics and Gynecology, University of Western Ontario, London, Canada;(4) Children’s Health Research Institute, University of Western Ontario, London, Canada |
| |
Abstract: | Fetal growth restriction (FGR) affects 3–5% of pregnancies and is associated with increased perinatal morbidity and mortality. Currently, there is no reliable biochemical test to differentiate a pathological FGR from a nonpathological one. The objective of this study was to screen whole maternal plasma to identify differentially expressed relatively abundant proteins associated with FGR. We analyzed maternal plasma from FGR (n=28) and healthy (n=22) pregnancies using two-dimensional gel electrophoresis (2D-GE) followed by software image analysis. Three spots with molecular weight (Mr) 18 kDa corresponding to haptoglobin (hp) α2, as identified by LC-MS/MS and immunoblotting, showed differential expression patterns in FGR. The distribution of hp α2 variants in maternal plasma samples showed the hp α2 variant 1 was low in 72% of FGR, medium in 16%, whereas high in 12%. In comparison, hp α2 variant 1 was high in (41%) of controls, medium in 41%, and low in 18% of cases. Based on the software image analysis, the mean spot volume for hp α2 variant 1 was 0.12 (SD=0.18) for FGR compared to 0.26 (SD=0.19) for control (p=0.006). Given that hp turnover is indicative of its maturation process and is traceable in plasma by its dominant/suppressed variants, we propose that hp α2 is an important potential target for evaluation of its clinical and pathophysiological role and as a diagnostic biomarker in FGR. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|