{"title":"Hemostatic parameters as hypercoagulability indicators in pregnancy","authors":"T. Vodnik, S. Ignjatović, N. Majkić-Singh","doi":"10.2298/JMH0302119V","DOIUrl":null,"url":null,"abstract":"The concentrations of plasma proteins involved in the process of coagulation are changed during the normal pregnancy, interfering with balance between procoagulant and anticoagulant systems. These changes include the increased activity of coagulation factors, the increased fibrin production and suppression of fibrinolysis. In this way, the risk of blood loss is reduced by physiological mechanisms, but the risk of thrombosis becomes higher. Thrombosis of placental blood vessels gives rise to placental insufficiency causing the repeated miscarriages, retardation of fetal growth, eclampsia intrauterine death of fetus and pre-term delivery. The causes of these incidents are the changes occurring within protein C coagulation system. The central anticoagulant enzyme is APC, which inactivates the activated factors V and VIII by proteolysis and, in that manner, inhibits the production of thrombin. The resistance to APC is the impairment of blood coagulation characterized by lower sensitivity to anticoagulant activity of APC. This disorder is in 95% of cases, caused by specific factor V gene point mutation and designated as F V Leiden. It is point mutation on locus 1691 where guanin is replaced by adenine what will lead to synthesis of modified F V molecule in which arginine is replaced by glutamine on locus 506. Arginine 506 is the locus of factor Xa binding, and it inhibits the inactivation of factor Va by the action of APC. The testing performed in pregnant women with regular and complicated pregnancy, in different periods, has shown that fibrinogen, fibrin monomer, TAT complex and PAI were good markers of hipercoagulability in pregnancy. The values of protein C activity were within normal limits. Protein S values were below lower limits. Global activity of protein C-anticoagulant pathway and its relation with procoagulant system were presented by quantitative measurement using Pro C Global test, while determination of activated protein C by means of APC sensitivity test was used for identification of persons with APC resistance e.g. with higher risk of thrombosis. Significantly lower PC-NR and APC-NR values were found in pregnant women with repeated miscarriages and in pregnant women with hypertension in relation to pregnant women with regular pregnancy. The results revealed significantly lower APC-anticoagulant activity in pregnancy, particularly in pregnancy associated with complications. Diagnostic accuracy of these parameters as markers of thrombotic changes in pregnancy was tested by ROC analysis. PC-NR and APC-NR showed satisfactory diagnostic accuracy as markers of thrombotic changes in pregnant women, more precisely, they were found to be good indicators of resistance to activated protein C in pregnancy.","PeriodicalId":287983,"journal":{"name":"Jugoslovenska Medicinska Biohemija-yugoslav Medical Biochemistry","volume":"12 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jugoslovenska Medicinska Biohemija-yugoslav Medical Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2298/JMH0302119V","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The concentrations of plasma proteins involved in the process of coagulation are changed during the normal pregnancy, interfering with balance between procoagulant and anticoagulant systems. These changes include the increased activity of coagulation factors, the increased fibrin production and suppression of fibrinolysis. In this way, the risk of blood loss is reduced by physiological mechanisms, but the risk of thrombosis becomes higher. Thrombosis of placental blood vessels gives rise to placental insufficiency causing the repeated miscarriages, retardation of fetal growth, eclampsia intrauterine death of fetus and pre-term delivery. The causes of these incidents are the changes occurring within protein C coagulation system. The central anticoagulant enzyme is APC, which inactivates the activated factors V and VIII by proteolysis and, in that manner, inhibits the production of thrombin. The resistance to APC is the impairment of blood coagulation characterized by lower sensitivity to anticoagulant activity of APC. This disorder is in 95% of cases, caused by specific factor V gene point mutation and designated as F V Leiden. It is point mutation on locus 1691 where guanin is replaced by adenine what will lead to synthesis of modified F V molecule in which arginine is replaced by glutamine on locus 506. Arginine 506 is the locus of factor Xa binding, and it inhibits the inactivation of factor Va by the action of APC. The testing performed in pregnant women with regular and complicated pregnancy, in different periods, has shown that fibrinogen, fibrin monomer, TAT complex and PAI were good markers of hipercoagulability in pregnancy. The values of protein C activity were within normal limits. Protein S values were below lower limits. Global activity of protein C-anticoagulant pathway and its relation with procoagulant system were presented by quantitative measurement using Pro C Global test, while determination of activated protein C by means of APC sensitivity test was used for identification of persons with APC resistance e.g. with higher risk of thrombosis. Significantly lower PC-NR and APC-NR values were found in pregnant women with repeated miscarriages and in pregnant women with hypertension in relation to pregnant women with regular pregnancy. The results revealed significantly lower APC-anticoagulant activity in pregnancy, particularly in pregnancy associated with complications. Diagnostic accuracy of these parameters as markers of thrombotic changes in pregnancy was tested by ROC analysis. PC-NR and APC-NR showed satisfactory diagnostic accuracy as markers of thrombotic changes in pregnant women, more precisely, they were found to be good indicators of resistance to activated protein C in pregnancy.
在正常妊娠期间,参与凝血过程的血浆蛋白浓度发生了变化,干扰了促凝剂和抗凝剂系统之间的平衡。这些变化包括凝血因子活性增加,纤维蛋白产生增加和纤维蛋白溶解抑制。这样,失血的风险通过生理机制降低,但血栓形成的风险却更高。胎盘血管血栓形成可引起胎盘功能不全,引起反复流产、胎儿发育迟缓、子痫、胎儿宫内死亡和早产。这些事件的原因是蛋白C凝血系统发生的变化。中心抗凝血酶是APC,它通过蛋白水解使活化因子V和VIII失活,从而抑制凝血酶的产生。对APC的耐药性是以对APC抗凝活性敏感性降低为特征的凝血功能损害。这种疾病占95%,由特定因子V基因点突变引起,命名为F V Leiden。基因座1691上鸟嘌呤被腺嘌呤取代的点突变导致基因座506上精氨酸被谷氨酰胺取代的修饰fv分子合成。精氨酸506是Xa因子结合位点,它通过APC的作用抑制Va因子的失活。对正常妊娠和复杂妊娠妇女在不同时期进行的检测表明,纤维蛋白原、纤维蛋白单体、TAT复合物和PAI是妊娠高凝性的良好标志物。蛋白C活性值在正常范围内。蛋白S值低于下限。采用Pro C Global试验定量测定蛋白C抗凝途径的整体活性及其与促凝系统的关系,而采用APC敏感性试验测定活化蛋白C用于鉴定APC耐药人群,如血栓形成风险高的人群。反复流产孕妇和高血压孕妇的PC-NR和APC-NR值明显低于正常妊娠孕妇。结果显示妊娠期apc抗凝活性明显降低,尤其是伴有并发症的妊娠期。这些参数作为妊娠期血栓变化标志物的诊断准确性通过ROC分析进行检验。PC-NR和APC-NR作为孕妇血栓形成变化的标志物具有满意的诊断准确性,更准确地说,它们被发现是妊娠对活化蛋白C抵抗的良好指标。