Chen Yu, Huang Ya-Juan
Department of Obstetrics and gynecology, Sixth Affiliated Hospital of Shanghai Jiaotong University, Shanghai 200233, China.
Zhonghua Fu Chan Ke Za Zhi. 2010 Oct;45(10):750-3.
to investigate apoptosis of placental syncytiotrophoblast in patients with early-onset and late-onset severe preeclampsia.
from November 2008 to May 2009, 15 cases with early-onset severe preeclampsia and 15 cases with late-onset severe preeclampsia matched with 10 women with normal pregnancies as control at Sixth Affiliated Hospital of Shanghai Jiaotong University were enrolled in this study. Enzyme-linked immunosorbent assay was used to measure syncytiotrophoblast microparticles (STBM) levels in peripheral venous plasma. Caspase-3 were measured by western blotting.
(1) STBM: the level of STBM of (71 ± 21) microg/L in early-onset group were significantly higher than (42 ± 30) microg/L in late-onset group and (26 ± 11) microg/L in control group (P < 0.05). The level of STBM in late-onset group and control group did not reach statistical difference (P > 0.05). (2) Caspase-3: the level of caspase-3 protein were 0.85 ± 0.61 in early-onset group and 0.77 ± 0.46 in late-onset group, which were all significantly higher than 0.32 ± 0.15 in control group (P < 0.05). However, the level of caspase-3 protein in early-onset group did not show remarkable difference compared with that in late-onset group (P > 0.05).
STBM are shed into the maternal circulation in higher amounts in early-onset preeclampsia, which indicated that early-onset and late-onset severe preeclampsia may have different etiology and pathogenesis.
探讨早发型和晚发型重度子痫前期患者胎盘合体滋养层细胞凋亡情况。
选取2008年11月至2009年5月在上海交通大学附属第六人民医院就诊的15例早发型重度子痫前期患者、15例晚发型重度子痫前期患者,以10例正常妊娠妇女作为对照组。采用酶联免疫吸附测定法检测外周静脉血浆中合体滋养层细胞微粒(STBM)水平,采用蛋白质印迹法检测Caspase-3水平。
(1)STBM:早发型组STBM水平为(71±21)μg/L,显著高于晚发型组的(42±30)μg/L和对照组的(26±11)μg/L(P<0.05)。晚发型组与对照组STBM水平差异无统计学意义(P>0.05)。(2)Caspase-3:早发型组Caspase-3蛋白水平为0.85±0.61,晚发型组为0.77±0.46,均显著高于对照组的0.32±0.15(P<0.05)。然而,早发型组与晚发型组Caspase-3蛋白水平差异无显著意义(P>0.05)。
早发型子痫前期患者母血中STBM水平较高,提示早发型和晚发型重度子痫前期可能具有不同的病因和发病机制。