Fernández F J, Rodríguez Pinto C, Páramo J, Cuesta B, Collado M, Rocha E
University Clinic of Navarra, Faculty of Medicine, University of Navarra, Pamplona, Spain.
Blood Coagul Fibrinolysis. 1990 Oct;1(4-5):571-5. doi: 10.1097/00001721-199010000-00043.
An abnormal fibrinogen was discovered in the plasma of a clinically asymptomatic woman. Laboratory evaluation of five members of the affected family showed low fibrinogen values in kinetic assays whereas the fibrinogen levels, tested by immunological procedures were normal. The patient's plasma had an inhibitory effect on the thrombin time of normal plasma. The calcium ions totally corrected the thrombin and reptilase times. Either low or high ionic strength prolonged the thrombin time of the proposita's purified fibrinogen. Kinetic analysis of clotting by monitoring transmission at 350 nm showed abnormally slow clotting with thrombin and reptilase. Assays were preformed in whole plasma as well as in purified fibrinogen. A delay in the rate of polymerization was evident when purified patient monomers were compared with those of normals. Immunoelectrophoretic, chromatofocusing, and isoelectrofusing experiments detected neither structural nor immunological abnormalities of fibrinogen. The rate of release of fibrinopeptide A by thrombin, measured by a specific immunoenzymatic method was also normal. HPLC analysis showed normal liberation of fibrinopeptides after prolonged thrombin action. Cross-linking of fibrin by factor XIII and lysis of fibrinogen by plasmin were normal. In view of these results, the defect of this dysfibrinogenemia, designated as Fibrinogen Oviedo I, probably could be due to conformational modifications in the D section of the molecule.
在一名临床无症状女性的血浆中发现了一种异常纤维蛋白原。对受影响家族的五名成员进行实验室评估,结果显示在动力学检测中纤维蛋白原值较低,而通过免疫程序检测的纤维蛋白原水平正常。患者血浆对正常血浆的凝血酶时间有抑制作用。钙离子完全纠正了凝血酶和蛇毒凝血酶时间。低离子强度或高离子强度都会延长先证者纯化纤维蛋白原的凝血酶时间。通过监测350nm处的吸光度对凝血进行动力学分析,结果显示凝血酶和蛇毒凝血酶导致的凝血异常缓慢。检测在全血浆以及纯化纤维蛋白原中进行。将纯化的患者单体与正常单体进行比较时,明显发现聚合速率延迟。免疫电泳、层析聚焦和等电聚焦实验均未检测到纤维蛋白原的结构或免疫异常。通过特定免疫酶法测定,凝血酶释放纤维蛋白肽A的速率也正常。HPLC分析显示,凝血酶长时间作用后纤维蛋白肽的释放正常。因子XIII介导的纤维蛋白交联和纤溶酶介导的纤维蛋白原裂解均正常。鉴于这些结果,这种被命名为纤维蛋白原奥维耶多I型的异常纤维蛋白原血症缺陷,可能是由于分子D区的构象修饰所致。