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血管紧张素转换酶基因缺失多态性作为髋关节置换术后的血栓形成风险因素。

Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty.

作者信息

Philipp C S, Dilley A, Saidi P, Evatt B, Austin H, Zawadsky J, Harwood D, Ellingsen D, Barnhart E, Phillips D J, Hooper W C

机构信息

Division of Hematology, UMDNJ-Robert Wood Johnson Medical School, New Brunswick, New Jersey 08904, USA.

出版信息

Thromb Haemost. 1998 Dec;80(6):869-73.

PMID:9869151
Abstract

Despite thromboprophylaxis, deep vein thrombosis is a common complication of major orthopedic surgery. Predisposing genetic risk factors are unknown. In this case-control study, we investigated the association of the insertion (I)/deletion (D) angiotensin converting enzyme (ACE) gene polymorphism, Factor V Leiden (R506Q) mutation, and 5,10 methylenetetrahydrofolate reductase (MTHFR) gene polymorphism with post-operative venous thrombosis in 85 patients who underwent elective total hip arthroplasty. The odds of a thrombotic event following hip surgery among subjects with the DD genotype of the ACE gene was increased more than 10-fold compared to subjects with the II genotype (odds ratio 11.7 [95% confidence interval 2.3-84.5]); it was increased 5-fold in subjects with the ID genotype compared to the II genotype (odds ratio 5.0 [95% confidence interval 1.1-34.9]). Mean plasma ACE level in control subjects not on ACE inhibitors at the time of study (n=43) was lowest in persons homozygous for the I allele (18.9+/-7.95 U/l), intermediate in patients with the ID genotype (31.6+/-10.8 U/l) and highest in subjects homozygous for the D allele (44.0+/-7.14 U/l). Mean plasma ACE level among cases was higher (33.0 U/l, n=25) than among controls (29.4 U/l, n=43) but this difference was not statistically significant. Neither the Factor V Leiden mutation nor MTHFR gene polymorphism increased the risk of thrombosis following hip replacement. These results demonstrate that the I/D ACE gene polymorphism is a potent risk factor for thrombosis in subjects undergoing total hip arthroplasty.

摘要

尽管采取了血栓预防措施,但深静脉血栓形成仍是大型骨科手术常见的并发症。其诱发的遗传风险因素尚不清楚。在这项病例对照研究中,我们调查了血管紧张素转换酶(ACE)基因插入(I)/缺失(D)多态性、凝血因子V莱顿(R506Q)突变以及5,10-亚甲基四氢叶酸还原酶(MTHFR)基因多态性与85例行择期全髋关节置换术患者术后静脉血栓形成之间的关联。与II基因型受试者相比,ACE基因DD基因型受试者髋关节手术后发生血栓事件的几率增加了10倍以上(比值比11.7 [95%置信区间2.3 - 84.5]);与II基因型相比,ID基因型受试者的几率增加了5倍(比值比5.0 [95%置信区间1.1 - 34.9])。在研究时未服用ACE抑制剂的对照受试者(n = 43)中,I等位基因纯合子个体的平均血浆ACE水平最低(18.9±7.95 U/l),ID基因型患者的水平居中(31.6±10.8 U/l),D等位基因纯合子个体的水平最高(44.0±7.14 U/l)。病例组的平均血浆ACE水平(33.0 U/l,n = 25)高于对照组(29.4 U/l,n = 43),但这种差异无统计学意义。凝血因子V莱顿突变和MTHFR基因多态性均未增加髋关节置换术后血栓形成的风险。这些结果表明,I/D ACE基因多态性是全髋关节置换术患者发生血栓形成的一个重要风险因素。

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