Department of Obstetrics and Gynaecology, The University of Melbourne, Sunshine Hospital, St Albans, 3021, Australia.
Department of Obstetrics and Gynaecology, The University of Melbourne, Sunshine Hospital, St Albans, 3021, Australia.
Placenta. 2019 Jan 15;76:6-9. doi: 10.1016/j.placenta.2018.12.007. Epub 2018 Dec 21.
Placental mediated fetal growth restriction (FGR) is a leading cause of perinatal morbidity and mortality. Heparan sulphate proteoglycans (HSPG) are highly expressed in placentae and regulate haemostasis. We hypothesise that altered expression of HSPGs, glypicans (GPC) may contribute to the development of FGR and small-for-gestational-age (SGA). GPC expression was determined in first-trimester chorionic villous samples collected from women with later SGA pregnancies and in placentae from third-trimester FGR and gestation-matched uncomplicated pregnancies. The expression of both GPC1 and GPC3 were significantly reduced in first-trimester SGA as well as in the third-trimester FGR placentae compared to controls. This is the first study to report a relationship between altered placental GPC expression and subsequent development of SGA/FGR.
胎盘介导的胎儿生长受限 (FGR) 是围产期发病率和死亡率的主要原因。硫酸乙酰肝素蛋白聚糖 (HSPG) 在胎盘组织中高度表达,并调节止血功能。我们假设 HSPG、聚糖 (GPC) 的表达改变可能导致 FGR 和小于胎龄儿 (SGA) 的发生。本研究通过检测妊娠晚期发生 SGA 孕妇的早孕期绒毛组织和 FGR 孕妇及同期正常妊娠孕妇的胎盘组织中 GPC 的表达情况,探讨 GPC 表达改变与 FGR 和 SGA 的关系。与对照组相比,早孕期 SGA 及孕晚期 FGR 胎盘组织中 GPC1 和 GPC3 的表达均显著降低。这是首次报道胎盘 GPC 表达改变与 SGA/FGR 发生相关的研究。