Department of Perinatology and Gynecology, Poznan University of Medical Sciences, 60-535 Poznan, Poland.
Department of Environmental Medicine, Poznan University of Medical Sciences, 61-848 Poznan, Poland.
Cells. 2022 Feb 18;11(4):724. doi: 10.3390/cells11040724.
Fetal growth restriction (FGR) is mainly caused by failure of the uteroplacental unit. The exact pathogenesis remains unclear. The cause is thought to be related to abnormal platelet activation, which may result in microthrombus formation in the small vessels of the placenta. Reactive oxygen species (ROS) may initiate the pathological process of platelet activation. This study aimed to evaluate selected platelet parameters in pregnancy complicated by FGR and relate them to the severity of hemodynamic abnormalities. A total of 135 women (pregnant with FGR, with an uncomplicated pregnancy, and non-pregnant) were enrolled to study different platelet parameters: count (PLT), mean volume (MPV), ROS levels, intracellular oxygen level, oxygen consumption, and aggregation indices. No abnormalities in PLT and MPV were found in the FGR group, although it revealed increased ROS levels in platelets, lower platelet oxygen consumption, and intraplatelet deprivation. Aggregation parameters were similar as in uncomplicated pregnancy. No significant relationships were observed between hemodynamic abnormalities and the studied parameters. Platelets in pregnancies complicated by FGR may reveal an impaired oxidative metabolism, which may, in turn, lead to oxidative stress and, consequently, to an impaired platelet function. This study adds to the understanding of the role of platelets in the etiology of FGR.
胎儿生长受限(FGR)主要是由于胎盘单位功能不全引起的。确切的发病机制尚不清楚。其病因可能与血小板异常激活有关,这可能导致胎盘小血管内微血栓形成。活性氧(ROS)可能引发血小板激活的病理过程。本研究旨在评估 FGR 妊娠中选定的血小板参数,并将其与血液动力学异常的严重程度相关联。共纳入了 135 名妇女(患有 FGR 的妊娠、无并发症的妊娠和非妊娠)来研究不同的血小板参数:计数(PLT)、平均体积(MPV)、ROS 水平、细胞内氧水平、耗氧量和聚集指数。尽管 FGR 组血小板中的 ROS 水平升高、血小板耗氧量降低和血小板内缺氧,但并未发现 PLT 和 MPV 异常。聚集参数与无并发症的妊娠相似。未观察到血液动力学异常与研究参数之间存在显著关系。FGR 妊娠中的血小板可能表现出氧化代谢受损,这反过来可能导致氧化应激,进而导致血小板功能受损。本研究增加了对血小板在 FGR 发病机制中作用的理解。