Hills F A, Gunn L K, Hardiman P, Thamaratnam S, Chard T
Department of Obstetrics, St. Bartholomew's Hospital Medical College, London,
Early Hum Dev. 1996 Jan 5;44(1):71-6. doi: 10.1016/0378-3782(95)01694-5.
Samples of maternal blood, amniotic fluid, placenta, fetal membranes and umbilical venous blood were collected from 59 women at vaginal delivery (32-41 weeks gestation) and 15 women at delivery by Caesarean section (37-41 weeks gestation). Umbilical vein levels of IGFBP-1 were significantly lower in deliveries prior to the onset of labour (elective Caesarean section) than those during normal vaginal delivery. These levels were, in turn, significantly lower than those delivered by emergency Caesarean section. This difference was not seen in any of the other tissues examined. Concentrations of IGFBP-1 were lower in placenta and membrane extracts from preterm deliveries than in term deliveries. This difference was not observed in maternal or fetal serum or in amniotic fluid. This study confirms that the fetal membranes are a major source of IGFBP-1 and that fetal circulating levels are raised where there is evidence of fetal hypoxia. The absence of a comparable rise in levels in placenta, membranes or amniotic fluid suggests that the origin of this increase is from fetal tissue.
从59名阴道分娩(妊娠32 - 41周)的女性和15名剖宫产分娩(妊娠37 - 41周)的女性中采集了母血、羊水、胎盘、胎膜和脐静脉血样本。分娩前(择期剖宫产)脐静脉中IGFBP - 1水平显著低于正常阴道分娩时的水平。而这些水平又显著低于急诊剖宫产分娩时的水平。在其他任何检测组织中均未观察到这种差异。早产时胎盘和胎膜提取物中IGFBP - 1的浓度低于足月产时。在母血或胎儿血清以及羊水中未观察到这种差异。本研究证实胎膜是IGFBP - 1的主要来源,并且在有胎儿缺氧证据的情况下胎儿循环水平会升高。胎盘、胎膜或羊水中水平没有出现类似升高,这表明这种升高的来源是胎儿组织。