Translational Obstetrics Group, Department of Obstetrics and Gynecology, Mercy Hospital for Women, Heidelberg, VIC, Australia.
Am J Obstet Gynecol. 2013 Aug;209(2):133.e1-9. doi: 10.1016/j.ajog.2013.04.011. Epub 2013 Apr 10.
To examine whether mRNA circulating in maternal blood coding genes regulating fetal growth are differentially expressed in (1) severe preterm fetal growth restriction (FGR) and (2) at 28 weeks' gestation in pregnancies destined to develop FGR at term.
mRNA coding growth genes were measured in 2 independent cohorts. The first was women diagnosed with severe preterm FGR (<34 weeks' gestation; n = 20) and gestation matched controls (n = 15), where the mRNA was measured in both maternal blood and placenta. The second cohort was a prospective longitudinal study (n = 52) of women whom had serial ultrasound assessments of fetal growth. mRNA coding growth genes in maternal blood were measured at 28 and 36 weeks in pregnancies with declining growth trajectories (ending up with term FGR; n = 10 among the 52 recruited) and controls who maintained normal growth trajectory (n = 15).
In women with severe preterm FGR, there was increased expression of placental growth hormone (6.3-fold), insulin-like growth factors (IGF1, 3.4-fold; IGF2, 5.0-fold), IGF receptors (2.1-fold) and IGF binding proteins (3.0-fold), and reduced expression of ADAM12 (0.5-fold) in maternal blood (and similar trends in placenta) compared with controls (P < .05). Notably, at 28 weeks' gestation there was increased IGF2 (3.9-fold), placental growth hormone (2.7-fold), and IGF BP2 (2.1-fold) expression in maternal blood in women destined to develop FGR at term (P < .05).
Measuring mRNA coding growth genes in maternal blood may detect unsuspected severe preterm FGR already present in utero, and predict term FGR when measured at 28 weeks' gestation.
检测母体外周血循环中编码胎儿生长调节基因的 mRNA 是否在(1)严重早产胎儿生长受限(FGR)和(2)妊娠 28 周时存在差异表达,这些孕妇最终会在足月时发生 FGR。
在 2 个独立队列中测量了 mRNA 编码生长基因。第一个队列包括被诊断为严重早产 FGR(<34 孕周;n=20)的女性和与之相匹配的对照组(n=15),其中母血和胎盘均测量了 mRNA。第二个队列是一项前瞻性纵向研究(n=52),对胎儿生长进行了连续超声评估。在有下降生长轨迹的孕妇(最终发展为足月 FGR;52 名招募孕妇中有 10 名属于此类;n=10)和维持正常生长轨迹的对照组(n=15)中,在 28 周和 36 周时测量了母血中编码生长基因的 mRNA。
与对照组相比,严重早产 FGR 孕妇的母血中胎盘生长激素(6.3 倍)、胰岛素样生长因子 1(IGF1,3.4 倍)、IGF2(5.0 倍)、IGF 受体(2.1 倍)和 IGF 结合蛋白(3.0 倍)表达增加,ADAM12(0.5 倍)表达减少(胎盘也有类似趋势;P<.05)。值得注意的是,在妊娠 28 周时,即将在足月时发生 FGR 的孕妇的母血中 IGF2(3.9 倍)、胎盘生长激素(2.7 倍)和 IGF BP2(2.1 倍)表达增加(P<.05)。
测量母血中编码生长基因的 mRNA 可能可以检测到子宫内已存在的未被察觉的严重早产 FGR,并在妊娠 28 周时测量时预测足月 FGR。