Department of Anatomy, Vardhman Mahavir Medical College and Safdarjang Hospital, New Delhi, India.
J Hum Hypertens. 2013 Feb;27(2):107-14. doi: 10.1038/jhh.2012.2. Epub 2012 Feb 23.
An imbalance between angiogenic and anti-angiogenic factors has been hypothesized to have a major role in hypertensive disorders during pregnancy, which account for significant morbidity and mortality for the mother and neonate in India. There is a paucity of information on soluble vascular endothelial growth factor receptor-1 (sVEGFR-1, anti-angiogenic factor) concentrations in different subgroups of pregnancy-induced hypertensive (PIH) disorders particularly in gestational hypertension (GH) and eclampsia during pregnancy. This cross-sectional study was conducted in order to test the above hypothesis and to get more insight into the role of sVEGFR-1 in these disorders. The concentrations of sVEGFR-1 in serum were measured from women with 22-39 weeks of gestation in the control (n=180) and gestationally matched hypertensive (n=360) pregnant mothers by ELISA. These sVEGFR-1 concentrations were found to be significantly elevated in the study groups as the severity of disease increases from GH to eclampsia (24 076 pg ml(-1); 42000 pg ml(-1), P=0.0001) as compared with controls (3360 pg ml(-1)). According to Receiver operating characteristic curve analysis, at ≤ 34 weeks, the concentration cutoff, sensitivity, specificity for sVEGFR-1 in differentiating GH, pre-eclampsia and eclampsia were ≥ 7619.2 pg ml(-1), 75%, 75%; ≥ 16726.6 pg ml(-1), 89.1%, 89.1%; ≥ 26222.8 pg ml(-1), 91.6%, 91.6%, respectively. The gradual upregulation of sVEGFR-1 concentrations in these groups may be due to its intimate involvement in the etiopathogenesis of severity of various hypertensive disorders by antagonizing effects of VEGF during the placental development. These observations indicate the clinical utility of sVEGFR-1 in differentiating PIH disorders and also will be helpful for the evaluation of increased monitoring system for successful pregnancy.
血管生成和抗血管生成因子之间的失衡被认为在怀孕期间的高血压疾病中起着重要作用,这在印度导致母亲和新生儿发病率和死亡率显著增加。在不同的妊娠相关性高血压疾病亚组中,包括妊娠期高血压疾病和子痫前期,可溶性血管内皮生长因子受体-1(抗血管生成因子)浓度的信息很少。这项横断面研究旨在检验上述假说,并更深入地了解 sVEGFR-1 在这些疾病中的作用。通过 ELISA 法测量了 22-39 周妊娠的对照组(n=180)和妊娠相关性高血压组(n=360)孕妇血清中 sVEGFR-1 的浓度。研究发现,随着疾病严重程度从妊娠期高血压疾病增加到子痫前期,sVEGFR-1 的浓度显著升高(24076 pg/ml;42000 pg/ml,P=0.0001),与对照组(3360 pg/ml)相比。根据接收者操作特征曲线分析,在≤34 周时,用于区分妊娠期高血压疾病、先兆子痫和子痫的 sVEGFR-1 浓度截断值、敏感性和特异性分别为≥7619.2 pg/ml、75%、75%;≥16726.6 pg/ml、89.1%、89.1%;≥26222.8 pg/ml、91.6%、91.6%。这些组中 sVEGFR-1 浓度的逐渐上调可能是由于其通过拮抗 VEGF 在胎盘发育过程中的作用,密切参与各种高血压疾病严重程度的发病机制。这些观察结果表明,sVEGFR-1 在区分妊娠相关性高血压疾病方面具有临床应用价值,也有助于评估增加的监测系统以实现成功妊娠。