Peking University Fourth School of Clinical Medicine, Beijing, China.
66526Beijing Jishuitan Hospital, Beijing, China.
Clin Appl Thromb Hemost. 2021 Jan-Dec;27:10760296211063877. doi: 10.1177/10760296211063877.
Deep venous thrombosis (DVT) is a common complication in patients with traumatic injury. Tissue factor pathway inhibitor (TFPI) is a natural anticoagulant protein in the extrinsic coagulation pathway. However, the relationship between DVT after trauma and the anticoagulant activity of TFPI remains unclear. In this prospective study, we investigated the role of TFPI in trauma patients with DVT to evaluate whether the anticoagulant activity of TFPI measured by a new functional assay can be used to help predict the risk of DVT. This prospective nested case-control study enrolled trauma patients and healthy volunteers. Forty-eight trauma patients diagnosed with DVT and forty-eight matched trauma patients without DVT were included in the study. 120 healthy volunteers were also included as controls. Blood samples and case information were collected at admission. Patients accepted angiography before surgery to diagnose DVT. The parameters examined included TFPI anticoagulant activity, free-TFPI antigen, blood cell counts, and routine clinical coagulation tests. For the parameters of TFPI anticoagulant activity, three were markedly increased in the DVT group compared to the non-DVT group (TFPI initial anticoagulant time ratio, P = .022; TFPI whole anticoagulant time ratio, P = .048; and TFPI anticoagulant rate, P = .034). The free-TFPI antigen concentration also showed a significant increasing trend in trauma patients with DVT compared with trauma patients without DVT (P = .035). Multivariate logistic regression analysis identified four independent factors for the development of DVT (TFPI initial anticoagulant time ratio, free-TFPI antigen, prothrombin time, and red blood cell count). We calculated the TFPI correlation coefficient and found that the area under the receiver operating characteristic curve was .821. A novel functional assay was developed to measure the anticoagulant activity of TFPI. The anticoagulant activity of TFPI can be used as a potential biomarker for diagnosing DVT in trauma patients.
深静脉血栓形成(DVT)是创伤患者的常见并发症。组织因子途径抑制剂(TFPI)是外源性凝血途径中的天然抗凝蛋白。然而,创伤后 DVT 与 TFPI 的抗凝活性之间的关系尚不清楚。在这项前瞻性研究中,我们研究了 TFPI 在创伤后 DVT 患者中的作用,以评估通过新的功能测定法测量的 TFPI 的抗凝活性是否可用于帮助预测 DVT 的风险。
这项前瞻性巢式病例对照研究纳入了创伤患者和健康志愿者。纳入了 48 例诊断为 DVT 的创伤患者和 48 例匹配的无 DVT 的创伤患者。还纳入了 120 名健康志愿者作为对照。入院时采集血样和病例资料。患者在手术前接受血管造影以诊断 DVT。检查的参数包括 TFPI 抗凝活性、游离 TFPI 抗原、血细胞计数和常规临床凝血试验。
对于 TFPI 抗凝活性的参数,与非 DVT 组相比,DVT 组有三个参数明显增加(TFPI 初始抗凝时间比,P=0.022;TFPI 全抗凝时间比,P=0.048;TFPI 抗凝率,P=0.034)。与无 DVT 的创伤患者相比,创伤后 DVT 患者的游离 TFPI 抗原浓度也呈显著升高趋势(P=0.035)。多变量逻辑回归分析确定了 DVT 发展的四个独立因素(TFPI 初始抗凝时间比、游离 TFPI 抗原、凝血酶原时间和红细胞计数)。我们计算了 TFPI 相关系数,发现接受者操作特征曲线下的面积为 0.821。开发了一种新的功能测定法来测量 TFPI 的抗凝活性。TFPI 的抗凝活性可作为诊断创伤患者 DVT 的潜在生物标志物。