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活化蛋白C抵抗试验可检测除因子V莱顿突变以外的血栓形成危险因素。

Activated protein C resistance assay detects thrombotic risk factors other than factor V Leiden.

作者信息

Graf Laurie L, Welsh Carolyn H, Qamar Zainab, Marlar Richard A

机构信息

Pathology Research Laboratory, Research Service, Denver Veterans Affairs Medical Center, 1055 Clermont St, Denver, CO 80220, USA.

出版信息

Am J Clin Pathol. 2003 Jan;119(1):52-60. doi: 10.1309/QCUU-NRMV-JY8M-WPPL.

Abstract

Activated protein C (APC) resistance is a common risk factor for venous thromboembolism (VTE) attributed to various mechanisms, including factor V Leiden (FVL) polymorphism. FVL is considered responsible for up to 95% of APC resistance; however, other factor V polymorphisms and elevated factor VIII levels also have been implicated. We assessed whether additional mechanisms contribute to APC resistance in a blinded case-control study of 65 subjects by measuring APC resistance using 3 methods: 2 activated partial thromboplastin time-based methods with and without dilution in factor V-deficient plasma and 1 Russell viper venom-based assay (RVV). Without factor V-deficient plasma, 24 subjects were APC resistant; with factor V-deficient plasma, the assay identified fewer APC-resistant subjects, as did RVV. All assays detected the 7 heterozygous FVL subjects. Thirteen subjects had factor VIII levels above 150% (1.50). After excluding subjects with FVL or elevated factor VIII levels, 4 subjects still had APC resistance. VTE risk trended higher for subjects with APC resistance in the absence of FVL. Measurement of APC resistance without dilution in factor V-deficient plasma is needed to assess for potentially important thrombotic risk factors other than FVL.

摘要

活化蛋白C(APC)抵抗是静脉血栓栓塞症(VTE)的常见危险因素,其归因于多种机制,包括因子V莱顿(FVL)多态性。FVL被认为导致高达95%的APC抵抗;然而,其他因子V多态性和因子VIII水平升高也与之有关。我们在一项对65名受试者的盲法病例对照研究中,通过3种方法测量APC抵抗,以评估是否有其他机制导致APC抵抗:2种基于活化部分凝血活酶时间的方法,分别在缺乏因子V的血浆中进行和不进行稀释,以及1种基于罗素蝰蛇毒的检测方法(RVV)。在不使用缺乏因子V的血浆时,24名受试者存在APC抵抗;使用缺乏因子V的血浆时,该检测方法识别出的APC抵抗受试者较少,RVV检测结果也是如此。所有检测方法都检测出了7名FVL杂合子受试者。13名受试者的因子VIII水平高于150%(1.50)。在排除FVL或因子VIII水平升高的受试者后,仍有4名受试者存在APC抵抗。在没有FVL的情况下,APC抵抗受试者的VTE风险有升高趋势。需要在不使用缺乏因子V的血浆进行稀释的情况下测量APC抵抗,以评估除FVL之外潜在的重要血栓形成危险因素。

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