Kristien Winckers, Eugenia Biguzzi, Stella Thomassen, Alexandra Heinzmann, Frits R Rosendaal, Tilman M Hackeng, Astrid van Hylckama-Vlieg
{"title":"Risk of First Venous Thrombosis by Comparing Different Thrombin Generation Assay Conditions: Results from the MEGA Case-control Study.","authors":"Kristien Winckers, Eugenia Biguzzi, Stella Thomassen, Alexandra Heinzmann, Frits R Rosendaal, Tilman M Hackeng, Astrid van Hylckama-Vlieg","doi":"10.1055/a-2534-6123","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hypercoagulability is a risk factor for venous thromboembolism (VTE). Thrombin generation (TG) is a global coagulation assay that measures an individual's clotting tendency. We hypothesise that slow-onset TG (achieved by using a low procoagulant stimulus or an inhibitor of coagulation) is the optimal responsive TG method for detecting hypercoagulability.This study aimed to compare different TG assay conditions with respect to VTE risk and assess the risk of the first VTE.</p><p><strong>Materials and methods: </strong>Basal TG at low tissue factor (TF) concentration and high TF concentration in the presence and absence of activated protein C (APC) were measured in plasma samples from 2,081 patients with first VTE and 2,908 healthy controls from the Multiple Environmental and Genetic Assessment of risk factors for venous thrombosis (MEGA) study. TG parameters and normalised activated protein C sensitivity ratio (nAPCsr) were categorised into quartiles as measured in the controls. We calculated odds ratios (ORs) with 95% confidence intervals (CIs) of the first VTE for different TG categories.</p><p><strong>Results: </strong>Under all assay conditions the thrombin peak height was associated with VTE risk: peak height of >75th percentile, at low TF OR 6.8 (95% CI 5.5-8.3), at high TF, OR 3.0 (95% CI 2.5-3.6), and at high TF + APC, OR 3.8 (95% CI 3.2-4.5), all compared with a peak height of <25th percentile obtained in controls. An increased nAPCsr (higher resistance to APC) was also associated with VTE risk, OR 3.4 (95% CI 2.8-4.1).</p><p><strong>Conclusion: </strong>Increased TG is associated with the risk of first VTE, particularly when triggered with a low procoagulant stimulus.</p>","PeriodicalId":94220,"journal":{"name":"TH open : companion journal to thrombosis and haemostasis","volume":"9 ","pages":"a25346123"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11924298/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"TH open : companion journal to thrombosis and haemostasis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2534-6123","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Hypercoagulability is a risk factor for venous thromboembolism (VTE). Thrombin generation (TG) is a global coagulation assay that measures an individual's clotting tendency. We hypothesise that slow-onset TG (achieved by using a low procoagulant stimulus or an inhibitor of coagulation) is the optimal responsive TG method for detecting hypercoagulability.This study aimed to compare different TG assay conditions with respect to VTE risk and assess the risk of the first VTE.
Materials and methods: Basal TG at low tissue factor (TF) concentration and high TF concentration in the presence and absence of activated protein C (APC) were measured in plasma samples from 2,081 patients with first VTE and 2,908 healthy controls from the Multiple Environmental and Genetic Assessment of risk factors for venous thrombosis (MEGA) study. TG parameters and normalised activated protein C sensitivity ratio (nAPCsr) were categorised into quartiles as measured in the controls. We calculated odds ratios (ORs) with 95% confidence intervals (CIs) of the first VTE for different TG categories.
Results: Under all assay conditions the thrombin peak height was associated with VTE risk: peak height of >75th percentile, at low TF OR 6.8 (95% CI 5.5-8.3), at high TF, OR 3.0 (95% CI 2.5-3.6), and at high TF + APC, OR 3.8 (95% CI 3.2-4.5), all compared with a peak height of <25th percentile obtained in controls. An increased nAPCsr (higher resistance to APC) was also associated with VTE risk, OR 3.4 (95% CI 2.8-4.1).
Conclusion: Increased TG is associated with the risk of first VTE, particularly when triggered with a low procoagulant stimulus.
背景:高凝是静脉血栓栓塞(VTE)的危险因素。凝血酶生成(TG)是一个全球性的凝血测定,测量一个人的凝血倾向。我们假设慢效TG(通过使用低促凝刺激或凝血抑制剂实现)是检测高凝性的最佳反应性TG方法。本研究旨在比较不同TG检测条件下静脉血栓栓塞的风险,并评估第一次静脉血栓栓塞的风险。材料和方法:在静脉血栓形成危险因素的多重环境和遗传评估(MEGA)研究中,对2081例首次静脉血栓形成患者和2908名健康对照者的血浆样本进行了低组织因子(TF)浓度和高组织因子浓度(APC)存在和不存在时的基础TG测定。TG参数和正常化活化蛋白C敏感性比(nAPCsr)被分类为四分位数,在对照组中测量。我们计算了不同TG类别的首次VTE的优势比(ORs)和95%置信区间(CIs)。结果:在所有检测条件下,凝血酶峰高与静脉血栓栓塞风险相关:峰高为>,第75百分位,低TF时OR为6.8 (95% CI 5.5-8.3),高TF时OR为3.0 (95% CI 2.5-3.6),高TF + APC时OR为3.8 (95% CI 3.2-4.5),均与峰高相比。结论:TG升高与首次静脉血栓栓塞风险相关,特别是在低促凝剂刺激下触发时。