孕妇子痫前期、妊娠期糖尿病和COVID-19中胎盘功能障碍的常见机制

S. Vari, O. Shevchuk, A. Boychuk, S. Kramar, Z. Nebesna, Y. Yakymchuk, L. Kobylinska, V. Chernyshenko, D. Korolova, A. Gaspar-Suranyi, T. Altorjay, R. Gáspár
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引用次数: 0

摘要

妊娠期COVID-19感染、先兆子痫和妊娠期糖尿病引起胎盘类似的变化,影响胎儿在妊娠期从受孕到出生的发育。适当的子宫和胎盘血管形成对胎儿的正常发育至关重要。胎盘交换是由胎盘内皮调节和维持的。在胎盘着床过程中,滋养细胞分化为两层,即内细胞滋养细胞层和外合胞滋养细胞层,它们是人类胎盘屏障的关键组成部分。促炎细胞因子加剧缺血事件,并在胎盘中产生一个向上螺旋的炎症反应。妊娠期COVID-19胎盘病理表现为滋养细胞脱屑、损伤和慢性组织细胞间绒毛炎。类似的病变也发生在妊娠期糖尿病和子痫前期。母亲的全身炎症反应,胎盘中炎症的增加和胎盘滋养细胞的细胞因子的产生应该在整个怀孕期间进行监测。胎盘血管生成可通过血清血管内皮生长因子、膜联蛋白A2、胎盘生长因子或硬化蛋白进行评估。组织损伤可通过测定血清乳酸脱氢酶和髓过氧化物酶水平来评估。三维多普勒可监测血流,苏木精和伊红染色石蜡包埋组织切片、电镜图像以及血管内皮生长因子、胎盘生长因子、硬化蛋白和膜联蛋白A2免疫组化检测可记录病理变化。母胎血管灌注损伤(绒毛炎和纤维蛋白沉积)是妊娠疾病的常见机制。胎盘病变释放抗内皮因子,导致抗血管生成状况,是妊娠疾病中母体胎盘血管灌注不良的常见机制。关键词:功能障碍,炎症,病理,胎盘,妊娠,血管形成
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Common mechanisms of placental dysfunction in preeclampsia, gestational diabetes, and COVID-19 in pregnant women
COVID-19 infection, preeclampsia and gestational diabetes mellitus in pregnancy cause similar changes in the placenta and influence development of the fetus between conception and birth in gestation. Proper uterine and placental vascularization is essential for normal fetal development. The transplacental exchange is regulated and maintained by the placental endothelium. During placental implantation, the trophoblast differentiates into two distinct layers, the inner cytotrophoblast and outer syncytiotrophoblast, which are key elements of the human placental barrier. Proinflammatory cytokines exacerbate ischemic events and create an upward spiral of an inflammatory reaction in the placenta. Placental pathology in gestational COVID-19 shows desquamation and damage of trophoblast and chronic histiocytic intervillositis. Similar lesions also occur in gestational diabetes mellitus and preeclampsia. The systemic inflammatory response of the mother, the increased inflammation in the placenta and cytokine production by placental trophoblasts should be monitored throughout pregnancy. Placental angiogenesis can be evaluated by serum vascular endothelial growth factor, Annexin A2, placental growth factor or sclerostin. Tissue damage can be assessed by measuring levels of serum lactate dehydrogenase and myeloperoxidase. Blood flow can be monitored with three-dimensional Doppler and pathological changes can be documented with paraffin-embedded tissue sections stained with hematoxylin and eosin, and electron microscope images as well as immunohistochemistry tests for vascular endothelial growth factor, placental growth factor, sclerostin and Annexin A2. The damage of maternal and fetal vascular perfusion (villitis and fibrin deposition) is a common mechanism of gestational diseases. The placenta lesions liberate anti-endothelial factors that lead to anti-angiogenic conditions and are the common mechanism of maternal placental vascular malperfusion in gestational diseases. Keywords: dysfunction, inflammation, pathology, placenta, pregnancy, vascularization
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