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本文引用的文献

1
High rate of in-stent restenosis after coronary intervention in carriers of the mutant mannose-binding lectin allele.突变型甘露糖结合凝集素等位基因携带者冠状动脉介入治疗后支架内再狭窄发生率高。
BMC Cardiovasc Disord. 2017 Jan 5;17(1):4. doi: 10.1186/s12872-016-0440-y.
2
THE ROLE OF POLYMORPHISM - 634 G/C (RS 2010963) OF VEGF-A GENE IN THE DEVELOPMENT OF HYPERTENSION AND OBESITY IN PREMENOPAUSAL WOMEN.血管内皮生长因子A基因多态性-634G/C(RS 2010963)在绝经前女性高血压和肥胖症发生中的作用
Georgian Med News. 2016 Jul(256-257):33-7.
3
Drug-Eluting or Bare-Metal Stents for Coronary Artery Disease.用于冠状动脉疾病的药物洗脱支架或裸金属支架
N Engl J Med. 2016 Sep 29;375(13):1242-52. doi: 10.1056/NEJMoa1607991. Epub 2016 Aug 29.
4
The Relationships between Polymorphisms in Genes Encoding the Growth Factors TGF-β1, PDGFB, EGF, bFGF and VEGF-A and the Restenosis Process in Patients with Stable Coronary Artery Disease Treated with Bare Metal Stent.编码生长因子转化生长因子-β1(TGF-β1)、血小板衍生生长因子B(PDGFB)、表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)和血管内皮生长因子-A(VEGF-A)的基因多态性与接受裸金属支架治疗的稳定型冠状动脉疾病患者再狭窄过程之间的关系。
PLoS One. 2016 Mar 1;11(3):e0150500. doi: 10.1371/journal.pone.0150500. eCollection 2016.
5
Vascular Endothelial Growth Factor Gene Polymorphism (rs2010963) and Its Receptor, Kinase Insert Domain-Containing Receptor Gene Polymorphism (rs2071559), and Markers of Carotid Atherosclerosis in Patients with Type 2 Diabetes Mellitus.2型糖尿病患者血管内皮生长因子基因多态性(rs2010963)及其受体含激酶插入结构域受体基因多态性(rs2071559)与颈动脉粥样硬化标志物
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Genetics of coronary artery disease and myocardial infarction.冠状动脉疾病和心肌梗死的遗传学
World J Cardiol. 2016 Jan 26;8(1):1-23. doi: 10.4330/wjc.v8.i1.1.
7
Association of Genetic Polymorphisms on Vascular Endothelial Growth Factor and its Receptor Genes with Susceptibility to Coronary Heart Disease.血管内皮生长因子及其受体基因的遗传多态性与冠心病易感性的关联
Med Sci Monit. 2016 Jan 4;22:31-40. doi: 10.12659/msm.895163.
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Vascular endothelial growth factor -2578C/A polymorphism and colorectal cancer risk: A meta-analysis.血管内皮生长因子-2578C/A多态性与结直肠癌风险:一项荟萃分析。
J Res Med Sci. 2015 Aug;20(8):811-7. doi: 10.4103/1735-1995.168406.
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Right Ventricular Adaptation Is Associated with the Glu298Asp Variant of the NOS3 Gene in Elite Athletes.精英运动员右心室适应性与NOS3基因的Glu298Asp变异有关。
PLoS One. 2015 Oct 30;10(10):e0141680. doi: 10.1371/journal.pone.0141680. eCollection 2015.
10
Association between the polymorphisms of the vascular endothelial growth factor gene and metabolic syndrome.血管内皮生长因子基因多态性与代谢综合征之间的关联
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裸金属支架冠状动脉介入治疗后VEGF基因多态性与支架内再狭窄的关联

Association between VEGF Gene Polymorphisms and In-Stent Restenosis after Coronary Intervention Treated with Bare Metal Stent.

作者信息

Bagyura Zsolt, Kiss Loretta, Hirschberg Kristóf, Berta Balázs, Széplaki Gábor, Lux Árpád, Szelid Zsolt, Soós Pál, Merkely Béla

机构信息

Heart and Vascular Center, Semmelweis University, Városmajor Utca 68, Budapest 1122, Hungary.

Department of Cardiology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.

出版信息

Dis Markers. 2017;2017:9548612. doi: 10.1155/2017/9548612. Epub 2017 Mar 7.

DOI:10.1155/2017/9548612
PMID:28484288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5412144/
Abstract

. In-stent restenosis (ISR) is the gradual narrowing of the vessel lumen after coronary stent implantation due to the increase in vascular smooth muscle cell proliferation. Vascular endothelial growth factor (VEGF) protein plays an important role in this process. Our aim was to analyze the association of single nucleotide polymorphisms of the VEGF gene (rs2010963 and rs6999447) with the occurrence of ISR after coronary artery bare metal stent (BMS) implantation. . 205 patients with a history of BMS implantation and a repeated coronarography were prospectively enrolled. Patients were assigned to diffuse restenosis group ( = 105) and control group ( = 100) and VEGF genotypes were determined. . Diffuse ISR was significantly more frequently observed in patients with homozygous normal genotype of rs2010963 polymorphism, and this polymorphism was independently associated with diffuse ISR. . RS2010963 is associated with higher incidence of development of diffuse coronary ISR in patients treated with BMS implantation.

摘要

支架内再狭窄(ISR)是冠状动脉支架植入后,由于血管平滑肌细胞增殖增加导致血管腔逐渐狭窄的过程。血管内皮生长因子(VEGF)蛋白在这一过程中起重要作用。我们的目的是分析VEGF基因单核苷酸多态性(rs2010963和rs6999447)与冠状动脉裸金属支架(BMS)植入后ISR发生的相关性。前瞻性纳入205例有BMS植入史且接受重复冠状动脉造影的患者。将患者分为弥漫性再狭窄组(n = 105)和对照组(n = 100),并确定VEGF基因型。rs2010963多态性纯合正常基因型患者中弥漫性ISR的发生率显著更高,且该多态性与弥漫性ISR独立相关。rs2010963与接受BMS植入治疗的患者发生弥漫性冠状动脉ISR的较高发生率相关。