腺苷脱氨酶基因(ADA) G22A变异与接受药物洗脱支架的冠状动脉支架内再狭窄的关系:简短的交流

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引用次数: 0

摘要

经皮冠状动脉介入治疗(PCI)中冠脉粥样硬化性狭窄的主要问题是支架内再狭窄(ISR)。在这项研究中,我们研究了腺苷脱氨酶基因(ADA)的G22A变体在ISR发展中的可能作用。本研究将91例行PCI的患者分为两组:支架植入术6个月后进行ISR的患者(n=40)和未进行ISR的对照组(n=51)。病例组和对照组在年龄和性别匹配方面进行匹配。采用分子PCR-RFLP法和电泳法检测样品中G22A变异的基因型,并采用t检验对结果进行统计学分析。本研究结果表明,变异G22A等位基因A在(+ ISR)组的频率高于(- ISR)组。然而,该变异的等位基因分布和基因型频率与ISR发病率无显著关系(p < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of G22A variant of Adenosine Deaminase gene (ADA) with coronary-in-stent restenosis in coronary artery patients receiving drug-eluting stent: Short Communication
The main problem with using stents in the treatment of coronary artery atherosclerotic stenosis in percutaneous coronary intervention (PCI) is In-stent restenosis (ISR). In this study, we investigated the possible role of the G22A variant of the Adenosine Deaminase gene (ADA) in the development of ISR. In this study, 91 patients who underwent PCI were divided into two groups: the case with ISR (n=40) and control without ISR after 6 months from stenting (n=51). The case and control groups were matched in terms of age and sex matching. The genotypes of the G22A variant in the samples were examined by the molecular method of PCR-RFLP and electrophoresis and the results were statistically analyzed by using t-test. The results of this study show that the frequency of allele A of variant G22A in (+ ISR) group is higher than (- ISR). However, there is no significant relationship between the distribution of allele and genotype frequency of this variant with the incidence of ISR (p>0.05).
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