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转录因子中的基因变异与接受华法林治疗患者的出血并发症。

Genetic variations in the transcription factors and and bleeding complications in patients receiving warfarin therapy.

作者信息

Yee Jeong, Kim Woorim, Chang Byung Chul, Chung Jee Eun, Lee Kyung Eun, Gwak Hye Sun

机构信息

College of Pharmacy & Division of Life and Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Korea.

College of Pharmacy, Chungbuk National University, Cheongju-si 28160, Korea.

出版信息

Drug Des Devel Ther. 2019 May 17;13:1717-1727. doi: 10.2147/DDDT.S198018. eCollection 2019.

Abstract

GATA4 and GATA6 are known to have potential roles in vascular regulation by affecting vascular smooth muscle cell differentiation and atrial natriuretic peptide levels. The aim of this retrospective study was to investigate the associations between and polymorphisms and bleeding complication risk at a therapeutic international normalized ratio (INR) in patients with mechanical heart valves. Study patients were included from the Ewha-Severance Treatment (EAST) Group of Warfarin. It consisted of 229 patients who received warfarin therapy after undergoing mechanical heart valve replacement and maintained a stable INR (INR of 2.0-3.0 for at least three consecutive times). Twenty single-nucleotide polymorphisms including , and were analyzed. Multivariate logistic regression analysis was employed to investigate the independent risk factors for bleeding complications. To evaluate the potential clinical value of genotyping for preventing bleeding complications in patients with high-risk genotype, the number needed to genotype (NNG) was also calculated. One hundred forty-two patients were included in this study, 21 of whom had bleeding complications. After adjusting covariates, TT genotype carriers of rs13273672 in and CC genotype carriers of rs10454095 in showed 5.0- (95% CI, 1.6-15.7) and 3.1-fold (95% CI, 1.1-8.7) higher bleeding complications than carriers of C allele and T allele, respectively. NNG for preventing one patient from experiencing bleeding complications in patients with TT genotype of rs13273672 and CC genotype of rs10454095 was 22.2 and 17.5, respectively. Patients with both TT genotype in rs13273672 and CC genotype in rs10454095 showed 8.7-fold (95% CI, 1.7-46.1) higher bleeding complications than those with other genotypes. NNG in patients having both TT genotype in rs13273672 and CC genotype in rs10454095 was calculated to be 40.0. This study showed that and gene polymorphisms could affect bleeding complications during warfarin treatment in patients with mechanical heart valves.

摘要

已知GATA4和GATA6通过影响血管平滑肌细胞分化和心钠素水平在血管调节中发挥潜在作用。这项回顾性研究的目的是调查机械心脏瓣膜置换术后患者在治疗性国际标准化比值(INR)时,[具体基因]和[具体基因]多态性与出血并发症风险之间的关联。研究患者来自延世大学Severance医院华法林治疗(EAST)组。该组由229例在接受机械心脏瓣膜置换术后接受华法林治疗且维持稳定INR(连续至少三次INR为2.0 - 3.0)的患者组成。分析了包括[具体基因]、[具体基因]和[具体基因]在内的20个单核苷酸多态性。采用多因素逻辑回归分析来研究出血并发症的独立危险因素。为评估基因分型在预防高危基因型患者出血并发症方面的潜在临床价值,还计算了基因分型所需数量(NNG)。本研究纳入了142例患者,其中21例发生出血并发症。在调整协变量后,[具体基因]中rs13273672的TT基因型携带者和[具体基因]中rs10454095的CC基因型携带者发生出血并发症的风险分别比C等位基因和T等位基因携带者高5.0倍(95%CI,1.6 - 15.7)和3.1倍(95%CI,1.1 - 8.7)。rs13273672的TT基因型和rs10454095的CC基因型患者预防一例出血并发症的NNG分别为22.2和17.5。rs13273672的TT基因型和rs10454095的CC基因型同时存在的患者发生出血并发症的风险比其他基因型患者高8.7倍(95%CI,1.7 - 46.1)。rs13273672的TT基因型和rs10454095的CC基因型同时存在的患者的NNG经计算为40.0。本研究表明,[具体基因]和[具体基因]基因多态性可能影响机械心脏瓣膜置换术后患者华法林治疗期间的出血并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/6529806/fa5939235c1a/DDDT-13-1717-g0001.jpg

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