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活化蛋白C抵抗的假性纯合性是静脉血栓形成的一个危险因素。

Pseudohomozygosity for activated protein C resistance is a risk factor for venous thrombosis.

作者信息

Castaman G, Tosetto A, Ruggeri M, Rodeghiero F

机构信息

Department of Haematology and the Haemophilia and Thrombosis Centre, San Bortolo Hospital, Vicenza, Italy.

出版信息

Br J Haematol. 1999 Jul;106(1):232-6. doi: 10.1046/j.1365-2141.1999.01502.x.

Abstract

Pseudohomozygosity for activated protein C resistance (APC-r) is a rare condition due to the association of heterozygous FV Leiden mutation and partial type I FV deficiency. To assess the risk of venous thromboembolism in these subjects, seven families including 11 pseudohomozygotes and 45 relatives were examined. Among the relatives, 16 were heterozygous FV Leiden carriers, nine showed partial FV deficiency and 20 no abnormalities. Deep vein thrombosis occurred in 4/11 (36.3%) pseudohomozygous patients versus 6/16 (37. 4%) FV Leiden carriers and 1/20 (5%) normal relatives. Pseudohomozygotes and FV Leiden carriers had a significantly increased risk of venous thrombosis in comparison to normal relatives (RR 8.8 and 5.7, respectively). There was no difference between the thrombotic risk of pseudohomozygous subjects and of FV Leiden carriers (RR 1.6, 95% CI 0.43-5.7). Furthermore, there was no difference in thrombosis-free survival between pseudohomozygotes and 45 consecutive FV Leiden heterozygous outpatients, suggesting that a referral bias may explain the apparent younger age of thrombosis in the pseudohomozygotes in comparison to relatives with FV Leiden heterozygosity (27 years v 54 years; P = 0.01). Pseudohomozygosity for APC resistance carries a significantly higher risk for venous thromboembolism in comparison to normal subjects, but probably not in comparison to heterozygous FV Leiden carriers.

摘要

活化蛋白C抵抗(APC-r)的假纯合子状态是一种罕见情况,它是由杂合子FV莱顿突变与部分I型FV缺乏症相关联所致。为评估这些受试者发生静脉血栓栓塞的风险,对7个家庭进行了检查,其中包括11名假纯合子和45名亲属。在亲属中,16名是FV莱顿杂合子携带者,9名表现为部分FV缺乏,20名无异常。11名假纯合子患者中有4名(36.3%)发生了深静脉血栓形成,而FV莱顿携带者中有6名(37.4%),正常亲属中有1名(5%)。与正常亲属相比,假纯合子和FV莱顿携带者发生静脉血栓形成的风险显著增加(相对风险分别为8.8和5.7)。假纯合子受试者与FV莱顿携带者的血栓形成风险之间没有差异(相对风险为1.6,95%可信区间为0.43 - 5.7)。此外,假纯合子与45名连续的FV莱顿杂合子门诊患者的无血栓生存期没有差异,这表明转诊偏倚可能解释了与FV莱顿杂合子亲属相比,假纯合子血栓形成的明显年轻年龄(27岁对54岁;P = 0.01)。与正常受试者相比,APC抵抗的假纯合子发生静脉血栓栓塞的风险显著更高,但与FV莱顿杂合子携带者相比可能并非如此。

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