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PAI-1 4G/5G 和 ACE DD 基因型的存在增加了血液透析患者早期动静脉瘘血栓形成的风险。

The presence of PAI-1 4G/5G and ACE DD genotypes increases the risk of early-stage AVF thrombosis in hemodialysis patients.

机构信息

Department of Internal Medicine, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.

出版信息

Ren Fail. 2011;33(2):169-75. doi: 10.3109/0886022X.2011.552151.

Abstract

BACKGROUND

In this study, we investigated the relationship between early arteriovenous fistula (AVF) thrombosis with angiotensin-converting enzyme (ACE) gene and thrombophilic factor gene polymorphisms.

METHODS

Thirty-five patients who suffered from three or more fistula thrombosis episodes in the early period after AVF operation and 33 control patients with no history of thrombosis for at least 3 years were enrolled in this study.

RESULTS

Factor V G1691A Leiden, factor V H1299R (R2), prothrombin G20210A, factor XIIIV34L, β-fibrinogen-455 G-A, glycoprotein IIIa L33P human platelet antigens (HPA-1), methylenetetrahydrofolate reductase C677T, and methylenetetrahydrofolate reductase A1298C gene polymorphisms were similar in both groups (p > 0.05). Plasminogen activator inhibitor 1 (PAI-1) 4G/5G genotype in the study group and 4G/4G genotype in the control group were significantly higher (p = 0.014). No significant difference was detected in terms of the 5G/5G genotype. With regard to the ACE gene polymorphism, the control group showed more ID genotype (19/33, 57.6%), whereas the study group showed more DD genotype (17/35, 48.6%). II genotype was similar in both groups (x(2) = 7.40, p = 0.025). The rate of ACE inhibitor-angiotensin II receptor blockers use was 5/35 in the study group (14.3%) and 5/33 in the control group (15.2%). Individuals with PAI-1 4G/5G genotype showed 5.03 times more risk of thrombosis when compared with 4G/4G and 5G/5G genotypes [p = 0.008, OR = 5.03, 95% confidence interval (1.44:17.64)]. Individuals with ACE DD genotype showed 4.25 times more risk of thrombosis when compared with II and ID [p = 0.008, OR = 4.25, 95% confidence interval (1.404:12.83)].

CONCLUSION

PAI-1 4G/5G and ACE DD genotypes are associated with increased risk for early AVF thrombosis.

摘要

背景

在这项研究中,我们研究了早期动静脉瘘(AVF)血栓形成与血管紧张素转换酶(ACE)基因和血栓形成因子基因多态性之间的关系。

方法

35 名患者在 AVF 手术后早期发生了 3 次或更多次瘘血栓形成,33 名对照组患者在至少 3 年内无血栓形成史,将这些患者纳入本研究。

结果

在两组中,因子 V G1691A 利得汶、因子 V H1299R(R2)、凝血酶原 G20210A、因子 XIIIV34L、β-纤维蛋白原-455 G-A、糖蛋白 IIIa L33P 人类血小板抗原(HPA-1)、亚甲基四氢叶酸还原酶 C677T 和亚甲基四氢叶酸还原酶 A1298C 基因多态性相似(p>0.05)。研究组中的纤溶酶原激活物抑制剂 1(PAI-1)4G/5G 基因型和对照组中的 4G/4G 基因型显著更高(p=0.014)。5G/5G 基因型没有差异。关于 ACE 基因多态性,对照组显示更多的 ID 基因型(19/33,57.6%),而研究组显示更多的 DD 基因型(17/35,48.6%)。两组 II 基因型相似(x(2)=7.40,p=0.025)。研究组 ACE 抑制剂-血管紧张素 II 受体阻滞剂的使用率为 5/35(14.3%),对照组为 5/33(15.2%)。与 4G/4G 和 5G/5G 基因型相比,PAI-1 4G/5G 基因型个体的血栓形成风险增加 5.03 倍[p=0.008,OR=5.03,95%置信区间(1.44:17.64)]。ACE DD 基因型个体的血栓形成风险比 II 和 ID 基因型个体增加 4.25 倍[p=0.008,OR=4.25,95%置信区间(1.404:12.83)]。

结论

PAI-1 4G/5G 和 ACE DD 基因型与早期 AVF 血栓形成风险增加相关。

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