Marcq G, Beaugrand Dubart L, Tournoys A, Subtil D, Deruelle P
Faculté de médecine Henri-Warembourg, université de Lille 2, PRES Nord de France, 59045 Lille, France.
Centre de biologie pathologique, CHRU de Lille, 59037 Lille, France.
Gynecol Obstet Fertil. 2014 Jun;42(6):393-8. doi: 10.1016/j.gyobfe.2012.09.019. Epub 2012 Oct 23.
Alterations in blood coagulation and fibrinolysis play a major role in the pathogenesis of preeclampsia. HELLP syndrome is associated with hypercoagulability and leads to maternal and perinatal complications. Our purpose was to evaluate D-dimer as a marker for severity in pregnancies with preeclampsia.
Plasma D-dimer levels were measured using an enzyme-linked immunosorbent assay (ELISA) technique. We studied the association between D-dimer levels and clinical and biological characteristics of pregnancies complicated by preeclampsia.
D-dimer values increased with increasing gestational age. Patients with HELLP syndrome had mean D-dimer values significantly greater than patients with preeclampsia alone (3848±2551 versus 1578±1077, P<0.001). However, the level of D-dimer at the time of admission was poorly predictive of occurrence of HELLP syndrome. Area under of the ROC curve was 0.69 (CI 95%: 0,59-0,79). The best threshold was 2170 ng/mL with a sensitivity of 0.91 and a specificity of 0.40. Other severity criteria of preeclampsia were not associated with higher levels of D-dimer.
In preeclamptic patients, D-dimer levels were related with gestational age and HELLP syndrome. However, accuracy of this test to predict occurrence of HELLP syndrome or severe preeclampsia was too low to recommend its use routinely.
凝血和纤溶的改变在子痫前期的发病机制中起主要作用。HELLP综合征与高凝状态相关,并导致孕产妇和围产期并发症。我们的目的是评估D-二聚体作为子痫前期妊娠严重程度的标志物。
采用酶联免疫吸附测定(ELISA)技术测量血浆D-二聚体水平。我们研究了D-二聚体水平与子痫前期合并妊娠的临床和生物学特征之间的关联。
D-二聚体值随孕周增加而升高。HELLP综合征患者的平均D-二聚体值显著高于单纯子痫前期患者(3848±2551对1578±1077,P<0.001)。然而,入院时D-二聚体水平对HELLP综合征发生的预测性较差。ROC曲线下面积为0.69(95%CI:0.59-0.79)。最佳阈值为2170 ng/mL,敏感性为0.91,特异性为0.40。子痫前期的其他严重程度标准与较高的D-二聚体水平无关。
在子痫前期患者中,D-二聚体水平与孕周和HELLP综合征有关。然而,该试验预测HELLP综合征或重度子痫前期发生的准确性过低,不建议常规使用。