Garcés María F, Vallejo Sergio A, Sanchez Elizabeth, Palomino-Palomino Miguel A, Leal Luis G, Ángel-Muller Edith, Díaz-Cruz Luz A, Ruíz-Parra Ariel Iván, González-Clavijo Angélica M, Castaño Justo P, Abba Martin, Lacunza Ezequiel, Diéguez Carlos, Nogueiras Rubén, Caminos Jorge E
Department of Physiology, School of Medicine, Universidad Nacional de Colombia, Bogotá, Colombia.
Department of Obstetrics and Gynecology, School of Medicine, Universidad Nacional de Colombia, Bogotá, Colombia.
Clin Endocrinol (Oxf). 2015 Aug;83(2):229-35. doi: 10.1111/cen.12715. Epub 2015 Feb 12.
Follistatin (FST) is a regulator of the biological activity of activin A (Act A), binding and blocking it, which could contribute to the modulation of its pro-inflammatory activity during pregnancy. We sought to investigate, in this nested case-control study, FST serum levels during normal pregnancy and correlate it with the FST profile in preeclamptic pregnant women, normal pregnant women followed 3 months postpartum and eumenorrheic nonpregnant women throughout the menstrual cycle.
Follistatin serum levels determined by ELISA, biochemical and anthropometric variables were measured in normal pregnant (n = 28) and preeclamptic (n = 20) women during three periods of gestation. In addition, FST serum levels were measured in a subset of normal pregnant women (n = 13) followed 3 months postpartum and in eumenorrheic nonpregnant women (n = 20) during the follicular and luteal phases of the menstrual cycle.
Follistatin serum levels in the eumenorrheic nonpregnant and postpartum group were significantly lower when compared to levels throughout gestation (P < 0·01). Serum FST levels increased in each period of pregnancy analysed, being significantly higher towards the end of gestation (P < 0·01). FST levels were lower in late pregnancy in preeclamptic women compared to normal pregnant women (P < 0·05). Finally, FST levels were higher in the luteal phase when compared with the follicular phase of the menstrual cycle (P < 0·05).
These analyses would permit the consideration that changes in FST levels during pregnancy contribute to the control of the Act A system.
卵泡抑素(FST)是激活素A(Act A)生物活性的调节剂,它能结合并阻断激活素A,这可能有助于调节其在孕期的促炎活性。在这项巢式病例对照研究中,我们试图调查正常孕期的FST血清水平,并将其与子痫前期孕妇、产后3个月随访的正常孕妇以及整个月经周期的正常月经非孕妇的FST情况进行关联。
通过酶联免疫吸附测定法(ELISA)测定卵泡抑素血清水平,在正常妊娠(n = 28)和子痫前期(n = 20)妇女的三个孕期测量生化和人体测量变量。此外,在产后3个月随访的一部分正常孕妇(n = 13)以及月经周期卵泡期和黄体期的正常月经非孕妇(n = 20)中测量FST血清水平。
与整个孕期相比,正常月经非孕妇和产后组的卵泡抑素血清水平显著降低(P < 0·01)。在分析的每个孕期,血清FST水平均升高,在妊娠末期显著更高(P < 0·01)。与正常孕妇相比,子痫前期妇女妊娠晚期的FST水平较低(P < 0·05)。最后,与月经周期的卵泡期相比,黄体期的FST水平更高(P < 0·05)。
这些分析结果使我们可以认为孕期FST水平的变化有助于控制激活素A系统。