Department of Gynecology and Obstetrics, First Affiliated Hospital, Medical School, Xi'an Jiaotong University, China.
Arch Med Sci. 2013 Aug 30;9(4):690-6. doi: 10.5114/aoms.2013.34989. Epub 2013 Apr 30.
Pre-eclampsia (PE) is the most serious syndrome of human pregnancy and it is potentially life-threatening for both mother and fetus. The aim of the study was to identify the role of high temperature requirement A1 (HtrA1) in pre-eclampsia.
One hundred consecutive pregnancies complicated by PE and 100 normal controls were included in our study. The changes in serum HtrA1 and fetal growth restriction were recorded. The placentae after delivery was also obtained for laboratory analyses.
High temperature requirement A1 expressed positively in all placenta tissues, but showed higher expression from control, PE with AGA (pre-eclamptic pregnancies with appropriate-for-gestational-age newborns) to PE with fetal growth restriction (FGR) groups. Early-onset PE happened more frequently while in PE with AGA, late-onset PE was more common. Additionally, we found that only during ∼28-32 gestational weeks, sera HtrA1 level of PE with AGA and PE with FGR was increased significantly compared with the control group (p < 0.05). In contrast, there was no significant difference between groups in other gestational ages in the third trimester (p > 0.05).
HtrA1 could potentially affect trophoblast migration and invasion during placentation, resulting in the shallow invasion noted in pre-eclampsia. HtrA1 may play an important role in the etiology and severity of PE and FGR. But the actual mechanism still needs deep research.
子痫前期(PE)是人类妊娠中最严重的综合征,对母婴均有潜在的生命威胁。本研究旨在探讨高热需求 A1(HtrA1)在子痫前期中的作用。
本研究纳入了 100 例连续妊娠并发 PE 和 100 例正常对照。记录血清 HtrA1 和胎儿生长受限的变化。分娩后还获得胎盘进行实验室分析。
HtrA1 在所有胎盘组织中均呈阳性表达,但在对照组、PE 合并适合胎龄儿(PE 合并 AGA)和 PE 合并胎儿生长受限(FGR)组中表达更高。早发型 PE 更常见,而在 PE 合并 AGA 中,晚发型 PE 更常见。此外,我们发现仅在约 28-32 孕周时,PE 合并 AGA 和 PE 合并 FGR 的血清 HtrA1 水平与对照组相比显著升高(p < 0.05)。相比之下,在妊娠晚期的其他孕龄组中,各组间 HtrA1 水平无显著差异(p > 0.05)。
HtrA1 可能在胎盘形成过程中影响滋养细胞的迁移和浸润,导致子痫前期中观察到的浅浸润。HtrA1 可能在 PE 和 FGR 的病因和严重程度中起重要作用。但实际机制仍需深入研究。