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Differential kinetics of serum and cervical insulin-like growth factor-binding protein-1 during mifepristone-misoprostol-induced medical termination of early pregnancy

机译:米非司酮-米索前列醇引起的早孕药物终止期间血清和宫颈胰岛素样生长因子结合蛋白-1的差异动力学

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The kinetics of cervical and circulating phosphoisoforms of insulin-like growth factor-binding protein-1 (IGFBP-1) in normal and pathological early pregnancy are not well known. We investigated the profiles of IGFBP-1 in serum and in cervical secretion during medical termination of early pregnancy. Sixteen women requesting termination of pregnancy, with <63 days of amenor-rhoea, received 200 mg of mifepristone on day 0, followed by either oral or vaginal administration of 0.8 mg of misoprostol on day 2. Serum and cervical swab samples, collected up to 6 weeks following the beginning of the treatment, were analysed for IGFBP-1 using two immunoenzymometric assays recognizing different patterns of IGFBP-1 phosphoisoforms. Serum mifepristone was also assayed. In the cervical samples, IGFBP-1 concentration, measured with both assays, increased substantially 2 days following administration of mifepristone. At 3 h after administration of misoprostol, IGFBP-1 had further increased several-fold in the cervix, but the increase was more pronounced as measured by the assay with preference for the amniotic fluid isoforms of IGFBP-1. A strong negative correlation was found between the time to abortion and the increase in cervical IGFBP-1 after administration of misoprostol, as measured by the assay preferring the phosphorylated isoforms of IGFBP-1. At 6 weeks, IGFBP-1 in the cervix had decreased to lower than pre-treatment levels, as measured by both assays. In serum, both assays showed a significant increase in IGFBP-1 concentrations after administration of mifepristone, and the highest values were measured on day 2, already before misoprostol administration. Thus, the kinetics of circulating and cervical IGFBP-1 differed from each other, indicating different sources and regulation of serum and cervical IGFBP-1.
机译:在正常和病理性早期妊娠中,胰岛素样生长因子结合蛋白-1(IGFBP-1)的子宫颈和循环磷酸同工酶的动力学尚不清楚。我们调查了早期妊娠医学终止过程中血清和宫颈分泌物中IGFBP-1的概况。 16名要求终止妊娠的妇女,其闭经少于63天,在第0天接受米非司酮200 mg,然后在第2天口服或经阴道给予0.8 mg米索前列醇,直至收集到开始治疗后6周,使用两种免疫酶法测定法分析IGFBP-1,以识别IGFBP-1磷酸同工型的不同模式。还测定了米非司酮的血清。在宫颈样品中,米非司酮给药后2天,两种测定法测得的IGFBP-1浓度均显着增加。米索前列醇给药后3小时,子宫颈中的IGFBP-1进一步增加了几倍,但这种增加更为明显,如偏爱IGFBP-1羊水同种型的测定所测。发现流产时间与服用米索前列醇后宫颈IGFBP-1的增加之间存在很强的负相关性,这是通过偏爱IGFBP-1磷酸化亚型的测定方法测得的。两种检测均显示,在第6周时,子宫颈中的IGFBP-1降低至低于治疗前水平。在血清中,两种测定均显示米非司酮给药后IGFBP-1浓度显着增加,并且在米索前列醇给药前第2天测得最高值。因此,循环和宫颈IGFBP-1的动力学互不相同,表明血清和宫颈IGFBP-1的来源和调节方式不同。

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