Division of Epidemiology & Community Health, University of Minnesota, Minneapolis, MN 55454, USA.
J Thromb Haemost. 2009 Oct;7(10):1639-48. doi: 10.1111/j.1538-7836.2009.03561.x. Epub 2009 Jul 28.
Thrombin is an enzyme that is essential for the acceleration of the coagulation cascade and the conversion of fibrinogen to clottable fibrin.
We evaluated the relationship of basal peak thrombin generation with the risk of future venous thromboembolism (VTE), and determined whether associations were independent of other coagulation markers.
The Longitudinal Investigation of Thromboembolism Etiology (LITE) study investigated VTE in two prospective population-based cohorts: the Atherosclerosis Risk in Communities (ARIC) study and the Cardiovascular Health Study (CHS). Peak thrombin generation was measured on stored plasma in a nested case-control sample (434 cases and 1004 controls). Logistic regression was used to estimate the relationship of peak thrombin generation with VTE, adjusted for age, sex, race, center, and body mass index. Mediation was evaluated by additionally adjusting for factor VIII and D-dimer.
Relative to the first quartile of peak thrombin generation, the odds ratio (OR) of VTE for those above the median was 1.74 [95% confidence interval (CI) 1.28-2.37]. The association was modestly attenuated by adjustment for FVIII and D-dimer (OR 1.47, 95% CI 1.05-2.05). Associations appeared to be stronger for idiopathic than for secondary VTE. Elevated peak thrombin generation more than added to the VTE risk associated with FV Leiden or low activated partial thromboplastin time.
In this prospective study of two independent cohorts, elevated basal peak thrombin generation was associated with subsequent risk of VTE, independently of established VTE risk factors.
凝血酶是一种酶,对于加速凝血级联反应和纤维蛋白原转化为可凝固的纤维蛋白至关重要。
我们评估了基础峰值凝血酶生成与未来静脉血栓栓塞 (VTE) 风险的关系,并确定了这些关联是否独立于其他凝血标志物。
血栓形成病因的纵向研究 (LITE) 研究调查了两个前瞻性基于人群的队列中的 VTE:动脉粥样硬化风险社区 (ARIC) 研究和心血管健康研究 (CHS)。在嵌套病例对照样本中(434 例病例和 1004 例对照),使用储存的血浆测量了峰值凝血酶生成。使用逻辑回归估计了峰值凝血酶生成与 VTE 的关系,调整了年龄、性别、种族、中心和体重指数。通过进一步调整因子 VIII 和 D-二聚体来评估中介作用。
与峰值凝血酶生成的第一四分位数相比,处于中位数以上的 VTE 的比值比 (OR) 为 1.74 [95%置信区间 (CI) 1.28-2.37]。通过调整 FVIII 和 D-二聚体,相关性略有减弱(OR 1.47,95%CI 1.05-2.05)。与继发性 VTE 相比,特发性 VTE 的相关性似乎更强。与 FV Leiden 或低激活部分凝血活酶时间相关的 VTE 风险相比,升高的峰值凝血酶生成更多地增加了 VTE 风险。
在这项对两个独立队列的前瞻性研究中,基础峰值凝血酶生成升高与随后的 VTE 风险相关,独立于已确立的 VTE 风险因素。