Li Yu, Chen Fang, Zhang Xiaoling, Gao Yuechun, Wu Changyan, Li Haiyan, Zhang Yuchen
Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University Chaoyang District 100029, Beijing, China.
Int J Clin Exp Pathol. 2015 Jun 1;8(6):7350-7. eCollection 2015.
Percutaneous coronary intervention (PCI) has been commonly used in the treatment of ischemic cardiovascular diseases, but the postprocedural in-stent restenosis (ISR) associated with altered endothelial functions has limited the clinical application of it; preventive medication with aspirin and statins has underlying adverse effects despite lowered risk of ISR. The purpose of this study was to investigate the role of angiotensin type 1 receptor (AT1R) A1166C gene polymorphisms in the development of endothelial dysfunction and ISR after PCI.
A total of 483 ST-segment elevation myocardial infarction (STEMI) patients undergoing PCI were prospectively genotyped using polymerase chain reaction (PCR) and restriction fragment length polymorphism assay. The demographic, clinical, laboratory and angiographic parameters were recorded peri-procedurally and the patients were followed within 3 years. The flow-mediated dilation (FMD) was used to reflect the short-term changes in endothelial functions among different genotypes. The significance of AT1R gene polymorphisms in the development of ISR was analyzed using univariable and multivariable models.
Amongst 483 patients, the distribution of the AT1R genotypes (AA, AC and CC) was associated with the levels of blood biomarkers of oxidative stress and deteriorated FMD after PCI (P<0.05). In univariable and multivariable logistic regression analysis, it was shown that AT1R CC genotype is strongly associated with the development of restenosis within 3 years after PCI (OR=3.736; P<0.001; calibrated OR=4.104; P<0.001).
The CC AT1R genotype was associated with deteriorated endothelial functions in the target vessels of PCI and intermediate to long-term ISR. Our findings contribute to the foundation of genome-based prevention for high risk groups of cardiovascular diseases and pretreatment for the patients undergoing PCI.
经皮冠状动脉介入治疗(PCI)已广泛应用于缺血性心血管疾病的治疗,但术后与内皮功能改变相关的支架内再狭窄(ISR)限制了其临床应用;阿司匹林和他汀类药物预防性用药虽降低了ISR风险,但存在潜在不良反应。本研究旨在探讨血管紧张素1型受体(AT1R)A1166C基因多态性在PCI术后内皮功能障碍和ISR发生中的作用。
对483例行PCI的ST段抬高型心肌梗死(STEMI)患者采用聚合酶链反应(PCR)和限制性片段长度多态性分析进行前瞻性基因分型。围手术期记录患者的人口统计学、临床、实验室和血管造影参数,并对患者进行3年随访。采用血流介导的血管舒张功能(FMD)反映不同基因型内皮功能的短期变化。使用单变量和多变量模型分析AT1R基因多态性在ISR发生中的意义。
在483例患者中,AT1R基因型(AA、AC和CC)的分布与PCI术后氧化应激血液生物标志物水平及FMD恶化相关(P<0.05)。单变量和多变量逻辑回归分析显示,AT1R CC基因型与PCI术后3年内再狭窄的发生密切相关(OR=3.736;P<0.001;校正OR=4.104;P<0.001)。
AT1R CC基因型与PCI靶血管内皮功能恶化及中远期ISR相关。我们的研究结果为心血管疾病高危人群的基因组预防和PCI患者的预处理奠定了基础。