Department of Vascular Surgery, Faculty of Medicine, School of Health Sciences, University of Thessalia, Larissa, Greece.
Thromb Res. 2013 Jul;132(1):47-50. doi: 10.1016/j.thromres.2013.05.017. Epub 2013 Jun 12.
Superficial vein thrombosis (SVT) is a common and controversial clinical entity. Recent studies have demonstrated that SVT should be seen as a venous thromboembolism (VTE). The objective of this study was to investigate the prevalence of thrombophilia defects and to estimate the role of age, sex and body mass index (BMI) in patients with varicose veins (VVs) and SVT.
A total of 230 patients with VVs, 128 with, and 102 without SVT underwent thrombophilia testing included factor V Leiden, prothrombin G20210A, methylenetetrahydrofolate reductase and plasminogen activator inhibitor- 1 mutations, protein C, protein S (PS), anti-thrombin III and plasminogen deficiencies and levels of A2 antiplasmin, activate protein C resistance and lupus anticoagulant. According to Clinical-Etiology-Anatomy-Pathophysiology (CEAP) classification patients were categorized in two subgroups: moderate disease (C2,3) and severe disease (C4,5,6). Age and body mass index were also assessed.
The prevalence of thrombophilia defects was significantly higher in patients with moderate disease and SVT (p=0.002). In the C2,3 group, SVT was associated with PS deficiency (p=0.018), obesity (p<0.001), male gender (p=0.047) and age (p<0.001). There were no significant differences in patients with severe disease.
Age, male sex, obesity and PS deficiency are factors associated with SVT development among patients with VVs having moderate disease (C2,3).
浅静脉血栓形成(SVT)是一种常见且有争议的临床病症。最近的研究表明,SVT 应被视为静脉血栓栓塞症(VTE)。本研究的目的是调查血栓形成倾向缺陷的发生率,并评估年龄、性别和体重指数(BMI)在静脉曲张(VVs)和 SVT 患者中的作用。
共有 230 例 VVs 患者,其中 128 例伴 SVT,102 例无 SVT,进行了血栓形成倾向检测,包括因子 V 莱顿、凝血酶原 G20210A、亚甲基四氢叶酸还原酶和纤溶酶原激活物抑制剂-1 突变、蛋白 C、蛋白 S(PS)、抗凝血酶 III 和纤溶酶原缺乏症以及 A2 抗纤溶酶、激活蛋白 C 抵抗和狼疮抗凝剂水平。根据临床-病因-解剖-病理生理学(CEAP)分类,患者分为两组:中度疾病(C2、3)和重度疾病(C4、5、6)。还评估了年龄和体重指数。
中度疾病和 SVT 患者的血栓形成倾向缺陷发生率明显更高(p=0.002)。在 C2、3 组中,SVT 与 PS 缺乏症(p=0.018)、肥胖(p<0.001)、男性性别(p=0.047)和年龄(p<0.001)相关。在重度疾病患者中没有显著差异。
年龄、男性、肥胖和 PS 缺乏症是与 VVs 中度疾病(C2、3)患者 SVT 发展相关的因素。