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首页> 外文期刊>European heart journal. Acute cardiovascular care >The 9p21 Rs 1333040 polymorphism is associated with coronary microvascular obstruction in ST-segment elevation myocardial infarction treated by primary angioplasty
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The 9p21 Rs 1333040 polymorphism is associated with coronary microvascular obstruction in ST-segment elevation myocardial infarction treated by primary angioplasty

机译:9P21 RS 1333040多态性与初级血管成形术治疗的ST段抬高心肌梗死中的冠状动脉微血管阻塞有关

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摘要

Background: Microvascular obstruction (MVO) after primary percutaneous coronary intervention (pPCI) leads to higher incidence of both early and late complications. A number of single nucleotide polymorphisms in 9p21 chromosome have been shown to affect angiogenesis in response to ischaemia. In particular, Rs1333040 with its three genotypic vriants C/C, T/C and T/T might influence the occurrence of MVO after pPCI. Methods: We enrolled ST-elevation myocardial infarction (STEMI) patients undergoing pPCI. The Rs1333040 polymorphism was evaluated by polymerase chain reaction-restriction fragment length polymorphism using restriction endonucleases (Bsml). Two expert operators unaware of the patients' identity performed the angiographic analysis; collaterals were assessed applying Rentrop's classification. Angiographic MVO was defined as a post-pPCI Thrombolysis In Myocardial Infarction (TIMI)<3 or TIMI 3 with myocardial blush grade 0 or 1, whereas electrocardiographic MVO was defined as ST segment resolution Results: Among our 133 STEMI patients (mean age 63 +/- 11 years, men 72%), 35 (26%) and 53 (40%) respectively experienced angiographic or electrocardiographic MVO. Angiographic and electrocardiographic MVO were different among the three variants (p= 0.03 and p=0.02 respectively). In particular, T/T genotype was associated with a higher incidence of both angiographic and electrocardiographic MVO compared with C/C genotype (p=0.04 and p=0.03 respectively). Moreover, Rentrop score <2 detection rate differed among the three genotypes (p=0.03). In particular T/T genotype was associated with a higher incidence of a Rentrop score <2 as compared with C/C genotype (p= 0.02). Conclusion: Rs1333040 polymorphism genetic variants portend different MVO incidence. In particular, T/T genotype is related to angiographic and electrocardiographic MVO and to worse collaterals towards the culprit artery.
机译:背景:初次经皮冠状动脉干预后的微血管阻塞(MVO)导致早期和后期并发症的发病率较高。已经显示出9p21染色体中的许多单核苷酸多态性,以应对血液血症影响血管生成。特别地,RS1333040具有三种基因型vriants C / C,T / C和T / T可能会影响PPCI后MVO的发生。方法:我们注册了在接受PPCI的ST升高心肌梗死(Stemi)患者。使用限制性内切核酸酶(BSML)通过聚合酶链反应限制片段长度多态性评估RS1333040多态性。两个专家运营商不知道患者的身份进行了血管造影分析;抵押品被评估适用伦敦的分类。血管造影MVO被定义为心肌梗死(TIMI)<3或TIMI 3的PPCI后溶栓,而心电图MVO被定义为ST分析结果:在我们的133名患者中(平均63 + / - 11年,男性72%),35(26%)和53(40%)分别经历过血管造影或心电图MVO。血管造影和心电图MVO在三种变体中不同(P = 0.03和P = 0.02)。特别地,与C / C基因型(P = 0.04和P = 0.03)相比,T / T基因型与血管造影和心电图MVO的发病率更高。此外,伦谱分数<2检测率在三种基因型中不同(P = 0.03)。特别地,与C / C基因型相比,T / T基因型与租圈分数<2的发病率较高(p = 0.02)。结论:RS1333040多态性遗传变异性分析不同的MVO发病率。特别地,T / T基因型与血管造影和心电图MVO有关,并且朝向罪魁祸首更差。

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