Lok Christine A R, Van Der Post Joris A M, Sargent Ian L, Hau Chi M, Sturk Augueste, Boer Kees, Nieuwland Rienk
Department of Obstetrics and Gynaecology, Academic Medical Center, Amsterdam, The Netherlands.
Hypertens Pregnancy. 2008;27(4):344-60. doi: 10.1080/10641950801955733.
Microparticles (MP) are pro-coagulant vesicles derived from various cells. Evidence is accumulating that MP are of pathophysiological relevance in autoimmune, cardiovascular, and thromboembolic diseases and inflammatory disorders. Therefore, their role in the development of preeclampsia was investigated and MP from preeclamptic patients influenced endothelial-dependent vasodilatation. Knowledge about changes in circulating MP numbers during pregnancy and preeclampsia is lacking. We determined this longitudinally and investigated whether these numbers related to the severity of preeclampsia.
Samples were obtained from pregnant women and preeclamptic patients during pregnancy and postpartum. MP were isolated and studied by flow cytometry.
During pregnancy, MP were decreased at 12 weeks gestation and then returned to postpartum values. In patients with preeclampsia, MP numbers were reduced at 28 and 36 weeks (both p = 0.04). Monocyte-derived MP were elevated in preeclampsia at 28 (p = 0.007), 32 (p = 0.02), and 36 weeks (p = 0.01), as were erythrocyte-derived MP at 28 weeks (p = 0.04). Placenta-derived MP increased in pregnancy and preeclampsia. During pregnancy, a correlation was present between placenta-derived MP and systolic blood pressure (r = 0.33, p = 0.015). No other correlations were found.
During pregnancy, numbers of MP initially decrease and subsequently normalize. Placenta-derived MP increase, possibly because of placental growth. In preeclampsia, reduced numbers of PMP are due to decreased platelet counts. Increased numbers of monocyte-derived MP reflect monocyte activation, which may be an expression of the systemic inflammation in preeclampsia. Lack of correlation between numbers of MP and severity of preeclampsia suggests that MP numbers alone do not explain the reported vascular effects of MP.
微粒(MP)是源自各种细胞的促凝血囊泡。越来越多的证据表明,MP在自身免疫性疾病、心血管疾病、血栓栓塞性疾病和炎症性疾病中具有病理生理学意义。因此,研究了它们在子痫前期发生发展中的作用,并且子痫前期患者的MP会影响内皮依赖性血管舒张。目前尚缺乏关于妊娠和子痫前期期间循环MP数量变化的知识。我们对此进行了纵向研究,并调查了这些数量是否与子痫前期的严重程度相关。
在孕期及产后从孕妇和子痫前期患者中采集样本。通过流式细胞术分离并研究MP。
在孕期,妊娠12周时MP数量减少,随后恢复至产后水平。子痫前期患者在妊娠28周和36周时MP数量减少(均p = 0.04)。子痫前期患者在妊娠28周(p = 0.007)、32周(p = 0.02)和36周(p = 0.01)时单核细胞衍生的MP升高,妊娠28周时红细胞衍生的MP也升高(p = 0.04)。胎盘衍生的MP在妊娠和子痫前期均增加。在孕期,胎盘衍生的MP与收缩压之间存在相关性(r = 0.33,p = 0.015)。未发现其他相关性。
在孕期,MP数量最初减少,随后恢复正常。胎盘衍生的MP增加,可能是由于胎盘生长。子痫前期中,胎盘微粒数量减少是由于血小板计数降低。单核细胞衍生的MP数量增加反映了单核细胞的激活,这可能是子痫前期全身炎症的一种表现。MP数量与子痫前期严重程度之间缺乏相关性表明,仅MP数量不能解释已报道的MP的血管效应。