Suarez C R, Gonzalez J, Menendez C, Fareed J, Fresco R, Walenga J
Loyola University Stritch School of Medicine, Department of Pediatric Hematology/Oncology, Maywood, Illinois.
Am J Hematol. 1988 Sep;29(1):18-21. doi: 10.1002/ajh.2830290105.
Determination of the plasma concentrations of beta-thromboglobulin (BTG), thromboxane B2 (TxB2) and platelet factor 4 (PF4) were made at the time of birth in 18 newborns and their respective mothers. Both groups show significant elevation of all these molecular markers, suggesting marked platelet activation. The elevated TxB2 levels in the newborn group, 25 +/- 8 pg/ml, are compatible with a normally functioning and activated platelet prostaglandin pathway. Mode of delivery, vaginal or caesarean section, does not significantly influence the degree of activation in either group. Ultrastructural platelet examination did not reveal any morphologic differences between maternal and newborn platelets. There appears to be marked activation of the newborn and maternal platelet systems at the time of birth, and we postulate that this may explain in part the transient platelet dysfunction observed in newborns.
对18名新生儿及其各自母亲在出生时测定了血浆β-血小板球蛋白(BTG)、血栓素B2(TxB2)和血小板因子4(PF4)的浓度。两组所有这些分子标志物均显著升高,提示血小板明显活化。新生儿组TxB2水平升高至25±8 pg/ml,与正常功能且活化的血小板前列腺素途径相符。分娩方式,即阴道分娩或剖宫产,对两组的活化程度均无显著影响。血小板超微结构检查未发现母体和新生儿血小板之间存在任何形态学差异。出生时新生儿和母体血小板系统似乎均有明显活化,我们推测这可能部分解释了新生儿中观察到的短暂血小板功能障碍。