Lenton E A, Grudzinskas J G, Gordon Y B, Chard T, Cooke I D
Acta Obstet Gynecol Scand. 1981;60(5):489-92. doi: 10.3109/00016348109155465.
Venous blood samples were collected prospectively in ten menstrual cycles where conception occurred, and for several weeks thereafter, and the circulating concentrations of pregnancy specific beta 1 glycoprotein (SP1) and human chorionic gonadotrophin (HCG) determined using specific radioimmunoassays. The data were converted to logarithms and pooled and pooled using the day of the LH peak as zero time. The concentration profiles so obtained were remarkable similar and showed a rapid exponential increase in concentration during the very early stage of pregnancy. The doubling times were 2.4 days and 2.3 days for SP1 and HCG respectively and both proteins were initially secreted in approximately equivalent concentrations. However, some 30 days following the LH peak, the concentration profiles began to diverge, with SP1 levels continuing to rise whilst HCG concentrations showed the characteristic plateau at 8 and 10 weeks of gestation.
前瞻性地收集了10个受孕月经周期的静脉血样本,并在之后的几周内持续收集,使用特定放射免疫分析法测定循环中的妊娠特异性β1糖蛋白(SP1)和人绒毛膜促性腺激素(HCG)浓度。数据转换为对数形式,并以促黄体生成素(LH)峰值日为零时间进行汇总。由此获得的浓度曲线非常相似,显示在妊娠早期浓度呈快速指数增长。SP1和HCG的倍增时间分别为2.4天和2.3天,两种蛋白最初分泌的浓度大致相当。然而,在LH峰值后约30天,浓度曲线开始出现差异,SP1水平持续上升,而HCG浓度在妊娠8周和10周时呈现出特征性的平台期。