首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Antiphospholipid antibodies and thrombosis: association with acquired activated protein C resistance in venous thrombosis and with hyperhomocysteinemia in arterial thrombosis.
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Antiphospholipid antibodies and thrombosis: association with acquired activated protein C resistance in venous thrombosis and with hyperhomocysteinemia in arterial thrombosis.

机译:抗磷脂抗体和血栓形成:在静脉血栓形成中与获得性活化蛋白C抵抗相关,在动脉血栓形成中与高同型半胱氨酸血症相关。

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摘要

Although antiphospholipid antibodies (aPL) are associated with thrombosis, it is not known who with aPL is at higher risk for thrombosis. It was the aim of this cross-sectional study to investigate how thrombophilic factors contribute to venous or arterial thrombosis in aPL-positive individuals. In outpatient test centres at two tertiary care hospitals, two hundred and eight (208) persons requiring aPL testing were matched by age, gender and centre to 208 persons requiring a complete blood count. Persons were classified as aPL-positive (having anticardiolipin, lupus anticoagulant and/or anti-beta(2)-glycoprotein I antibodies) or aPL-negative. Several thrombophilic factors were studied using logistic regression modelling. Results showed that the aPL-positive group had three-fold more events (37%) than the aPL-negative group (12%). In unadjusted analyses, clinically important associations were observed between factor V Leiden and venous thrombosis, hyperhomocysteinemia and arterial thrombosis, and activated protein C resistance (APCR) and venous thrombosis (OR, 95% CI = 4.00, 1.35-11.91; 4.79, 2.03-11.33; and 2.03, 1.03-3.97, respectively). After adjusting for recruitment group, persons with both APCR and aPL had a three-fold greater risk (OR, 95% CI = 3.31, 1.30-8.41) for venous thrombosis than those with neither APCR nor aPL. Similarly, after adjusting for hypertension, family history of cardiovascular disease, gender and recruitment group, persons with both hyperhomocysteinemia and aPL had a five-fold increased risk (OR, 95% CI = 4.90, 1.37-17.37) for arterial thrombosis compared to those with neither risk factor. In conclusion, APCR phenotype and hyperhomocysteinemia are associated with a higher risk of venous and arterial thrombosis, respectively, in the presence of aPL.
机译:尽管抗磷脂抗体(aPL)与血栓形成有关,但尚不清楚谁患有aPL的血栓形成风险更高。这项横断面研究的目的是调查血栓形成性因素如何导致aPL阳性个体的静脉或动脉血栓形成。在两家三级医院的门诊测试中心中,需要进行aPL测试的一百零八(208)人按年龄,性别和中心进行了匹配,有208人需要进行全血细胞计数。人被分类为aPL阳性(具有抗心磷脂,狼疮抗凝和/或抗β(2)-糖蛋白I抗体)或aPL阴性。使用logistic回归模型研究了几个血栓形成因素。结果显示,aPL阳性组的事件(37%)是aPL阴性组的事件(12%)多三倍。在未经调整的分析中,观察到V因子莱顿与静脉血栓形成,高同型半胱氨酸血症和动脉血栓形成,活化蛋白C抵抗性(APCR)和静脉血栓形成之间存在重要的临床关联(OR,95%CI = 4.00,1.35-11.91; 4.79,2.03- 11.33;和2.03,1.03-3.97)。在调整了招募组之后,同时使用APCR和aPL的患者发生静脉血栓形成的风险(既不使用APCR也没有aPL的患者)高三倍(OR,95%CI = 3.31,1.30-8.41)。同样,在对高血压,心血管疾病的家族病史,性别和招募组进行调整之后,高同型半胱氨酸血症和aPL的人的动脉血栓形成风险增加了五倍(OR,95%CI = 4.90,1.37-17.37)没有危险因素。总之,在存在aPL的情况下,APCR表型和高同型半胱氨酸血症分别与较高的静脉和动脉血栓形成风险相关。

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