首页> 外文期刊>Journal of research in medical sciences : >PLASMA CONCENTRATION, GENETIC VARIATION, AND GENE EXPRESSION LEVELS OF MATRIX METALLOPROTEINASE 9 IN IRANIAN PATIENTS WITH CORONARY ARTERY DISEASE
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PLASMA CONCENTRATION, GENETIC VARIATION, AND GENE EXPRESSION LEVELS OF MATRIX METALLOPROTEINASE 9 IN IRANIAN PATIENTS WITH CORONARY ARTERY DISEASE

机译:伊朗冠心病患者血浆中金属蛋白酶9的血浆浓度,遗传变异和基因表达水平

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Background: Matrix metalloproteinase 9 (MMP9) ?1562C>T (rs3918242) polymorphism has been proposed as a risk factor forcoronary artery disease (CAD) with conflicting results. The aim of the present study was to investigate the association of ?1562C>Tgenetic polymorphism, gene expression and circulating levels of MMP9 with CAD risk in an Iranian subpopulation in in Zanjan City.Materials and Methods: This was a retrospective case–control study we investigated retrospectively 100 patients with angiographicallyverified CAD and 100 matched controls. Genotyping of ?1562C>T polymorphism was done by polymerase chain reaction?restrictionfragment length polymorphism (PCR?RFLP). Gene expression levels and circulating levels of MMP9 was determined by real?timereverse transcription?PCR and enzyme immunoassay method, respectively. Statistical analysis was done using Student’s t?test orChi?square test by SPSS 16 software.Results: The mean circulating levels of MMP9 were significantly higher in CAD Group thancontrol group (P=0.002). Mean plasma levels of MMP9 were also significantly higher in triple vessel stenosis patients than doublevessel or single vessel stenosis patients (P T polymorphism (P=0.002, P=0.01, respectively). However, genotypeand allele frequencies of MMP9 ?1562C>T polymorphism were similar between CAD patients and controls (P>0.05). Additionally, the ?1562C>T polymorphism of MMP9 gene didn’t increase the risk of CAD in dominant (P=0.537) or recessive (P=0.249) geneticmodels.Conclusion: Our study demonstrated that circulating levels of MMP9 but not ?1562C>T polymorphism of MMP9 genemay be a risk factor for development and severity of CAD in an Iranian subpopulation in Zanjan.
机译:背景:基质金属蛋白酶9(MMP9)?1562C> T(rs3918242)多态性已被认为是冠状动脉疾病(CAD)的危险因素,其结果相互矛盾。本研究的目的是探讨赞亚市伊朗亚人群中?1562C> T基因多态性,基因表达和MMP9的循环水平与CAD风险的关系。材料与方法:这是一项回顾性病例对照研究。回顾性研究了100例经血管造影验证的CAD患者和100例匹配的对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对1562C> T多态性进行基因分型。 MMP9的基因表达水平和循环水平分别通过实时逆转录PCR和酶联免疫法测定。使用SPSS 16软件通过学生t检验或卡方检验进行统计分析。结果:CAD组MMP9的平均循环水平显着高于对照组(P = 0.002)。三支血管狭窄患者的平均血浆MMP9水平也明显高于双支血管或单支血管狭窄患者(PT多态性(分别为P = 0.002,P = 0.01),但MMP9〜1562C> T多态性的基因型和等位基因频率相似。在CAD患者和对照组之间(P> 0.05),此外,MMP9基因的?1562C> T多态性不会增加显性(P = 0.537)或隐性(P = 0.249)基因模型的CAD风险。证明了循环水平的MMP9而非MMP9基因的?1562C> T多态性可能是Zanjan伊朗亚人群CAD发生和严重程度的危险因素。

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