Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Star-Medical Diagnostic Center, Rotterdam, the Netherlands.
J Thromb Haemost. 2017 Mar;15(3):500-506. doi: 10.1111/jth.13611. Epub 2017 Feb 15.
Essentials Differences in sensitivity to factor VII (FVII) have been suggested between thromboplastins. FVII-induced International Normalized Ratio (INR) changes differ between commercial reagents. Recombinant human thromboplastins are more sensitive to FVII than tissue-extract thromboplastins. Thromboplastin choice may affect FVII-mediated INR stability.
Background Differences regarding sensitivity to factor VII have been suggested for recombinant human and tissue-extract thromboplastins used for International Normalized Ratio (INR) measurement, but the evidence is scarce. Differences in FVII sensitivity are clinically relevant, as they can affect INR stability during treatment with vitamin K antagonists (VKAs). Objectives To determine whether commercial thromboplastins react differently to changes in FVII. Methods We studied the effect of addition of FVII on the INR in plasma by using three tissue-extract (Neoplastin C1+, Hepato Quick, and Thromborel S) and three recombinant human (Recombiplastin 2G, Innovin, and CoaguChek XS) thromboplastins. Three different concentrations of purified human FVII (0.006, 0.012 and 0.062 μg mL plasma), or buffer, were added to five certified pooled plasmas of patients using VKAs (INR of 1.5-3.5). Changes in FVII activity were measured with two bioassays (Neoplastin and Recombiplastin), and relative INR changes were compared between reagents. Results After addition of 0.062 μg mL FVII, FVII activity in the pooled plasmas increased by approximately 20% (Neoplastin) or 32% (Recombiplastin) relative to the activity in pooled normal plasma. All thromboplastins showed dose-dependent INR decreases. The relative INR change in the pooled plasmas significantly differed between the six thromboplastins. No differences were observed among recombinant or tissue-extract thromboplastins. Pooled results indicated that the FVII-induced INR change was greater for recombinant than for tissue-extract thromboplastins. Conclusions Differences regarding FVII sensitivity exist between various thromboplastins used for VKA monitoring. Recombinant human thromboplastins are more sensitive to FVII than tissue-extract thromboplastins. Therefore, thromboplastin choice may affect FVII-mediated INR stability.
比较不同商业试剂中凝血酶原时间(PT)试剂对维生素 K 拮抗剂(VKA)治疗患者凝血酶原时间(PT)国际标准化比值(INR)的影响。
我们研究了三种组织提取(Neoplastin C1+、Hepato Quick 和 Thromborel S)和三种重组人(Recombiplastin 2G、Innovin 和 CoaguChek XS)PT 试剂在添加不同浓度的人凝血因子 VII(0.006、0.012 和 0.062 μg/ml 血浆)或缓冲液时对五份使用 VKA 的患者认证混合血浆的 INR 的影响。使用两种生物测定法(Neoplastin 和 Recombiplastin)测量添加 FVII 后混合血浆中 FVII 活性的变化,并比较试剂之间的相对 INR 变化。
添加 0.062 μg/ml FVII 后,混合血浆中的 FVII 活性相对于混合正常血浆中的活性增加了约 20%(Neoplastin)或 32%(Recombiplastin)。所有的 PT 试剂均显示出剂量依赖性的 INR 降低。混合血浆中各试剂之间的相对 INR 变化差异显著。重组或组织提取的 PT 试剂之间无差异。汇总结果表明,与组织提取的 PT 试剂相比,重组人凝血酶原时间(PT)试剂对 FVII 的诱导 INR 变化更敏感。
不同的 PT 试剂在用于 VKA 监测时对 FVII 敏感性存在差异。重组人凝血酶原时间(PT)试剂比组织提取的 PT 试剂对 FVII 更敏感。因此,PT 试剂的选择可能会影响 FVII 介导的 INR 稳定性。