Matsumoto T, Shima M, Takeyama M, Yoshida K, Tanaka I, Sakurai Y, Giles A R, Yoshioka A
Department of Pediatrics, Nara Medical University, Nara, Japan.
J Thromb Haemost. 2006 Feb;4(2):377-84. doi: 10.1111/j.1538-7836.2006.01730.x.
Precise assessment of clotting function is essential for monitoring of hemostatic treatment for hemophilias A and B.
Clot waveform analysis and thrombin generation assays were performed on factor (F) VIII- and FIX-deficient plasmas, which had been reconstituted with known amounts of recombinant FVIII (rFVIII) and affinity-purified FIX respectively. Clot waveforms were assessed qualitatively and quantitatively by measuring the parameters clotting time, maximum coagulation velocity (Min1), and maximum coagulation acceleration (Min2). The thrombin generation assay was also assessed qualitatively and measurements made of time to peak and peak height.
Overall results obtained with both assays showed good correlation for both clotting factors confirming that the changes in clotting waveform reflected changes in thrombin generation. Both assays demonstrated a predictable dose response to the addition of FVIII or IX. However, clot waveform analysis was more sensitive than the thrombin generation assay, particularly in detecting very low levels (0-0.1 IU dL(-1)) of both factors.
These data suggest that the application of clot waveform analysis to the routine management of the hemophiliacs could increase our understanding of the clinical significance of low levels of FVIII and FIX that cannot be measured by assays in current use. This may be particularly useful in the management of hemophiliacs with inhibitors or undergoing gene therapy.
精确评估凝血功能对于监测甲型和乙型血友病的止血治疗至关重要。
对分别用已知量的重组FVIII(rFVIII)和亲和纯化FIX重构的VIII因子和IX因子缺乏血浆进行凝血波形分析和凝血酶生成测定。通过测量凝血时间、最大凝血速度(Min1)和最大凝血加速度(Min2)等参数对凝血波形进行定性和定量评估。还对凝血酶生成测定进行了定性评估,并测量了达到峰值的时间和峰值高度。
两种测定方法获得的总体结果显示,两种凝血因子的结果具有良好的相关性,证实凝血波形的变化反映了凝血酶生成的变化。两种测定方法均显示出对添加FVIII或IX的可预测剂量反应。然而,凝血波形分析比凝血酶生成测定更敏感,尤其是在检测两种因子的极低水平(0 - 0.1 IU dL(-1))时。
这些数据表明,将凝血波形分析应用于血友病患者的常规管理可能会增进我们对目前所用测定方法无法测量的低水平FVIII和FIX临床意义的理解。这在有抑制剂或正在接受基因治疗的血友病患者管理中可能特别有用。