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TGF-β1 多态性增加心脏瓣膜置换术后口服抗凝患者出血并发症的风险。

TGF-β1 polymorphism increases the risk of bleeding complications in patients on oral anticoagulant after cardiac valve replacement.

机构信息

College of Pharmacy, Chungbuk National University, 660-1, Yeonje-ri, Osong-eup, Heungdeok-gu, Cheongju-si, 28160, Korea.

College of Pharmacy & Division of Life and Pharmaceutical Sciences, Ewha Womans University, 52 Ewhayeodae-gil, Seodaemun-gu, Seoul, 03760, Korea.

出版信息

Heart Vessels. 2021 Dec;36(12):1885-1891. doi: 10.1007/s00380-021-01867-2. Epub 2021 May 13.

Abstract

Although an elevated INR is highly associated with an increased risk of warfarin-associated bleeding, it has been reported that some patients also experience bleeding complications at therapeutic INRs. TGF-β1 polymorphisms has been reported to cause vascular malformations, resulting in bleeding complications, but there are few published genetic studies regarding bleeding complications in patients on warfarin therapy. This study aimed to determine if there is an association between transforming growth factor beta-1 (TGF-β1) polymorphisms and bleeding complications in patients who maintain international normalized ratios (INRs) of 2.0-3.0 with warfarin therapy after cardiac valve replacement. Eleven single nucleotide polymorphis (SNPs) of TGF-β1 (rs1800469, rs2241718, rs4803455, rs2241717, rs2241716, rs2241715, rs2241714, rs11083616, rs2317130, rs747857, and rs1982073) were analyzed. Univariate and multivariable analyses were conducted to evaluate the associations between genetic polymorphisms and bleeding risk. Attributable risk and the number needed to genotype (NNG) were calculated to identify the potential clinical value of genotyping. A discrimination of model was assessed via an analysis of the area under the receiver operating curve (AUROC). To test the model's goodness of fit, a Hosmer-Lemeshow test was performed. Of 142 patients, 21 experienced bleeding complications. Among analyzed single nucleotide polymorphis (SNPs) of TGF-β1 (rs1800469, rs2241718, rs4803455, rs2241717, rs2241716, rs2241715, rs2241714, rs11083616, rs2317130, rs747857, and rs1982073), AA genotype carriers in rs2241718 had about 5.5 times more bleeding complications than those with the G allele after adjusting for other confounders. The attributable risk and NNG for rs2241718 were 81.9% and 57.8, respectively. The presence of atrial fibrillation and myocardial infarction increased bleeding complications 3.9- and 9.8-fold, compared with those without atrial fibrillation and myocardial infarction, respectively. Bleeding complications during warfarin therapy in patients with mechanical heart valves were associated with TGF-β1 polymorphisms as well as atrial fibrillation and myocardial infarction.

摘要

尽管 INR 升高与华法林相关出血的风险高度相关,但据报道,一些患者在治疗 INR 时也会出现出血并发症。TGF-β1 多态性已被报道可导致血管畸形,从而导致出血并发症,但关于华法林治疗患者出血并发症的遗传研究较少。本研究旨在确定转化生长因子β-1(TGF-β1)多态性与心脏瓣膜置换术后 INR 维持在 2.0-3.0 的华法林治疗患者出血并发症之间是否存在关联。分析了 TGF-β1 的 11 个单核苷酸多态性(SNP)(rs1800469、rs2241718、rs4803455、rs2241717、rs2241716、rs2241715、rs2241714、rs11083616、rs2317130、rs747857 和 rs1982073)。进行了单变量和多变量分析,以评估遗传多态性与出血风险之间的关系。计算归因风险和基因型数量(NNG),以确定基因分型的潜在临床价值。通过分析接收者操作特征曲线(AUROC)下的面积来评估模型的区分能力。为了检验模型的拟合优度,进行了 Hosmer-Lemeshow 检验。在 142 名患者中,有 21 名发生出血并发症。在分析的 TGF-β1(rs1800469、rs2241718、rs4803455、rs2241717、rs2241716、rs2241715、rs2241714、rs11083616、rs2317130、rs747857 和 rs1982073)单核苷酸多态性中,与 G 等位基因相比,rs2241718 的 AA 基因型携带者在调整其他混杂因素后发生出血并发症的风险约增加 5.5 倍。rs2241718 的归因风险和 NNG 分别为 81.9%和 57.8。与无房颤和心肌梗死的患者相比,房颤和心肌梗死患者的出血并发症分别增加 3.9 倍和 9.8 倍。机械心脏瓣膜患者华法林治疗期间的出血并发症与 TGF-β1 多态性以及房颤和心肌梗死有关。

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