van Veen Joost J, Gatt Alex, Bowyer Annette E, Cooper Peter C, Kitchen Steve, Makris Mike
Sheffield Haemophilia and Thrombosis Centre, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, United Kingdom.
Thromb Res. 2009 Apr;123(6):895-901. doi: 10.1016/j.thromres.2008.09.011. Epub 2008 Nov 13.
Global coagulation tests may have a better relation with phenotype in haemophilia than traditional coagulation tests. These include the Calibrated Automated Thrombin generation assay (CAT) and modified thromboelastometry using low tissue factor triggering. Both have shown marked variability in thrombin generation and clot formation profiles respectively despite similar FVIII:C levels and have been suggested as means to monitor treatment. Data with modified thromboelastometry are largely limited to severe and moderate haemophiliacs. CAT measurements in haemophilia are generally performed at low TF concentrations (1 pM) because of a higher sensitivity for the intrinsic pathway at this concentration but is also sensitive for FVIII at higher concentrations (5 pM) and this has the advantage that inhibition of contact factor activation can be avoided. No formal comparison of both TF concentrations has been reported and the data on modified thromboelastometry in mild haemophilia are limited.
In this study we compared thrombin generation at 1 and 5 pM in 57 haemophilia patients without exposure to treatment and 41 patients after treatment. We also assessed the sensitivity of thromboelastometry for haemophilia A in 29 patients.
We found that CAT discriminates well between normal individuals and haemophilia patients; also FVIII:C correlates well with the ETP/peak. We found no clear advantages of measurements at 1 compared to 5 pM but found increased variation over time at 1 pM. The sensitivity of modified thromboelastometry for haemophilia A was less than CAT with abnormal measurements largely limited to severe and moderate patients. Larger studies correlating both methods with clinical outcome are required.
与传统凝血检测相比,全球凝血检测可能与血友病的表型有更好的相关性。这些检测包括校准自动凝血酶生成测定法(CAT)和使用低组织因子触发的改良血栓弹力图法。尽管FVIII:C水平相似,但两者分别在凝血酶生成和血凝块形成曲线方面均显示出显著差异,并被建议作为监测治疗的手段。改良血栓弹力图法的数据主要限于重度和中度血友病患者。由于在此浓度下对内源性途径具有更高的敏感性,血友病患者的CAT测量通常在低组织因子浓度(1 pM)下进行,但在较高浓度(5 pM)下对FVIII也敏感,这具有可以避免接触因子激活抑制的优点。尚未报道两种组织因子浓度的正式比较,且轻度血友病中改良血栓弹力图法的数据有限。
在本研究中,我们比较了57例未接受治疗的血友病患者和41例接受治疗后的患者在1 pM和5 pM时的凝血酶生成情况。我们还评估了29例患者中血栓弹力图法对甲型血友病的敏感性。
我们发现CAT能很好地区分正常个体和血友病患者;此外,FVIII:C与内源性凝血酶潜能/峰值相关性良好。我们发现与5 pM相比,1 pM测量没有明显优势,但发现1 pM时随时间的变化增加。改良血栓弹力图法对甲型血友病的敏感性低于CAT,异常测量主要限于重度和中度患者。需要进行更大规模的研究,将这两种方法与临床结果相关联。