Kühne T, Ryan G, Blanchette V, Semple J W, Hornstein A, Mody M, Chang W, McWhirter L, Freedman J
Division of Hematology, St Michael's Hospital, Toronto, Ontario, Canada.
Pediatr Res. 1996 Dec;40(6):876-80. doi: 10.1203/00006450-199612000-00018.
Preeclampsia, a common complication of pregnancy, contributes significantly to maternal and fetal morbidity and mortality. It may lead to both quantitative and qualitative defects of maternal and neonatal platelets. In this prospective study, flow cytometry has been used to study expression of platelet-surface glycoproteins (GPs) on maternal and neonatal platelets of both healthy and preeclamptic subjects. We studied 15 preeclamptic women, 20-44 y of age, and their newborns (median gestational age, 32 wk; range, 26-38) and seven healthy women (aged 26-41 y) and their healthy newborns (median gestational age, 38 wk; range, 38-42). Compared with their healthy and preeclamptic mothers, resting platelets from neonates expressed significantly less CD41 and CD9. Thrombin activation resulted in significant increases in platelet-surface expression of CD62P, CD63, CD41, CD9, and CD36 in neonates and their healthy mothers. Compared with neonates of healthy mothers, platelets from neonates of preeclamptic mothers expressed lower levels of CD62P, CD63, CD9, and CD36 on activated platelets. These findings suggest that preeclampsia influences the expression of platelet-surface GPs on neonatal and maternal platelets, which may affect platelet function, leading to an additional risk for bleeding in thrombocytopenic neonates of mothers with preeclampsia.
子痫前期是一种常见的妊娠并发症,对母婴发病率和死亡率有重大影响。它可能导致母体和新生儿血小板出现数量和质量上的缺陷。在这项前瞻性研究中,流式细胞术被用于研究健康和子痫前期患者的母体及新生儿血小板表面糖蛋白(GPs)的表达。我们研究了15名年龄在20 - 44岁的子痫前期女性及其新生儿(中位胎龄32周;范围26 - 38周),以及7名健康女性(年龄26 - 41岁)及其健康新生儿(中位胎龄38周;范围38 - 42周)。与健康和子痫前期的母亲相比,新生儿的静息血小板表达的CD41和CD9明显较少。凝血酶激活导致新生儿及其健康母亲的血小板表面CD62P、CD63、CD41、CD9和CD36表达显著增加。与健康母亲的新生儿相比,子痫前期母亲的新生儿血小板在激活后CD62P、CD63、CD9和CD36的表达水平较低。这些发现表明,子痫前期会影响新生儿和母体血小板表面GPs的表达,这可能会影响血小板功能,导致子痫前期母亲的血小板减少新生儿出现额外的出血风险。