Chaiworapongsa Tinnakorn, Espinoza Jimmy, Gotsch Francesca, Kim Yeon Mee, Kim Gi Jin, Goncalves Luis F, Edwin Samuel, Kusanovic Juan Pedro, Erez Offer, Than Nandor Gabor, Hassan Sonia S, Romero Roberto
Perinatology Research Branch, National Institute of Child Health and Human Development, NIH/DHHS, Bethesda, MD 20892, USA.
J Matern Fetal Neonatal Med. 2008 Jan;21(1):25-40. doi: 10.1080/14767050701832833.
The soluble form of vascular endothelial growth factor receptor-1 (sVEGFR-1), an antagonist to vascular endothelial growth factor and placental growth factor, has been implicated in the pathophysiology of preeclampsia. Preeclampsia and pregnancy complicated with small for gestational age (SGA) fetuses share some pathophysiologic derangements, such as failure of physiologic transformation of the spiral arteries, endothelial cell dysfunction, and leukocyte activation. The objectives of this study were to: (1) determine whether plasma concentrations of sVEGFR-1 in mothers with SGA fetuses without preeclampsia at the time of diagnosis are different from those in patients with preeclampsia or normal pregnant women, and (2) examine the relationship between plasma concentrations of sVEGFR-1 and Doppler velocimetry in uterine and umbilical arteries in patients with preeclampsia and those with SGA.
A cross-sectional study was conducted to determine the concentrations of the soluble form of VEGFR-1 in plasma obtained from normal pregnant women (n = 135), women with SGA fetuses (n = 53), and patients with preeclampsia (n = 112). Patients with SGA fetuses and those with preeclampsia were sub-classified according to the results of uterine and umbilical artery Doppler velocimetry examinations. Plasma concentrations of sVEGFR-1 were determined by an ELISA. Since these concentrations change with gestational age, differences among various subgroups were statistically estimated with the delta value, defined as the difference between the observed and expected plasma sVEGFR-1 concentration. The expected values were derived from regression analysis of plasma sVEGFR-1 concentrations in normal pregnancy. Regression analysis and univariate and multivariate analysis were employed.
(1) Mothers with SGA fetuses had a mean plasma concentration of sVEGFR-1 higher than normal pregnant women (p < 0.001), but lower than patients with preeclampsia (p < 0.001). (2) Among patients with SGA fetuses, only those with abnormal uterine artery Doppler velocimetry had a mean plasma sVEGFR-1 concentration significantly higher than normal pregnant women (p < 0.001). (3) Among mothers with SGA fetuses in whom Doppler velocimetry was performed (n = 41), those with abnormalities in both the uterine and umbilical artery velocimetry had the highest mean delta of sVEGFR-1 plasma concentration (mean +/- standard deviation (SD): 0.69 +/- 0.29). Conversely, patients who had normal Doppler velocimetry in both uterine and umbilical arteries had the lowest mean delta (mean +/- SD: 0.09 +/- 0.29) of sVEGFR-1 plasma concentrations (ANOVA; p < 0.001). (4) Among patients with preeclampsia in whom Doppler velocimetry was performed (n = 69), those with abnormalities in both the uterine and umbilical artery velocimetry had the highest mean delta sVEGFR-1 plasma concentration (mean +/- SD: 1.01 +/- 0.22) among all groups classified (ANOVA; p < 0.001). (5) Among patients with SGA and those with preeclampsia, there was a relationship (Chi-square for trend p < 0.001 for both) between the severity of Doppler velocimetry abnormalities and the proportion of patients who had high delta sVEGFR-1 plasma concentrations (defined as a concentration two standard deviations (2SD) above the mean delta of normal pregnant women). (6) Multiple regression analysis suggested that the diagnostic category (e.g., SGA or preeclampsia), Doppler abnormalities, and gestational age at blood sampling were associated with an increase in plasma sVEGFR-1 concentrations (p < 0.001).
These observations provide support for the participation of the soluble receptor of vascular endothelial growth factor in the pathophysiology of SGA with abnormal uterine artery Doppler velocimetry and preeclampsia. An excess of sVEGFR-1 is released into the maternal circulation of patients with preeclampsia and those with SGA fetuses, as abnormalities of impedance to blood flow involve uterine and umbilical circulation.
血管内皮生长因子受体-1(sVEGFR-1)的可溶性形式是血管内皮生长因子和胎盘生长因子的拮抗剂,与子痫前期的病理生理学有关。子痫前期和妊娠合并小于胎龄(SGA)胎儿有一些共同的病理生理紊乱,如螺旋动脉生理性转化失败、内皮细胞功能障碍和白细胞活化。本研究的目的是:(1)确定诊断时无子痫前期的SGA胎儿母亲血浆中sVEGFR-1浓度是否与子痫前期患者或正常孕妇不同;(2)研究子痫前期患者和SGA患者血浆中sVEGFR-1浓度与子宫和脐动脉多普勒测速之间的关系。
进行了一项横断面研究,以确定从正常孕妇(n = 135)、SGA胎儿孕妇(n = 53)和子痫前期患者(n = 112)获得的血浆中VEGFR-1可溶性形式的浓度。SGA胎儿孕妇和子痫前期患者根据子宫和脐动脉多普勒测速检查结果进行亚分类。通过酶联免疫吸附测定法(ELISA)测定血浆中sVEGFR-1的浓度。由于这些浓度随孕周变化,各亚组之间的差异用差值进行统计学估计,差值定义为观察到的和预期的血浆sVEGFR-1浓度之间的差异。预期值来自正常妊娠血浆sVEGFR-1浓度的回归分析。采用回归分析以及单因素和多因素分析。
(1)SGA胎儿母亲的血浆sVEGFR-1平均浓度高于正常孕妇(p < 0.001),但低于子痫前期患者(p < 0.001)。(2)在SGA胎儿孕妇中,只有子宫动脉多普勒测速异常的患者血浆sVEGFR-1平均浓度显著高于正常孕妇(p < 0.001)。(3)在进行了多普勒测速的SGA胎儿母亲中(n = 41),子宫和脐动脉测速均异常的母亲血浆sVEGFR-1浓度的平均差值最高(平均值±标准差(SD):0.69±0.29)。相反,子宫和脐动脉多普勒测速均正常的患者血浆sVEGFR-1浓度的平均差值最低(平均值±SD:0.09±0.29)(方差分析;p < 0.001)。(4)在进行了多普勒测速的子痫前期患者中(n = 69),子宫和脐动脉测速均异常的患者血浆sVEGFR-1浓度的平均差值在所有分类组中最高(平均值±SD:1.01±0.22)(方差分析;p < 0.001)。(5)在SGA胎儿孕妇和子痫前期患者中,多普勒测速异常的严重程度与血浆sVEGFR-1浓度差值高的患者比例之间存在相关性(两者趋势的卡方检验p < 0.001)(定义为高于正常孕妇平均差值两个标准差(2SD)的浓度)。(6)多因素回归分析表明,诊断类别(如SGA或子痫前期)、多普勒异常和采血时的孕周与血浆sVEGFR-1浓度升高有关(p < 0.001)。
这些观察结果支持血管内皮生长因子可溶性受体参与子宫动脉多普勒测速异常的SGA和子痫前期的病理生理学过程。子痫前期患者和SGA胎儿孕妇的母体循环中释放了过量的sVEGFR-1,因为血流阻抗异常涉及子宫和脐循环。