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Analysis of the correlation between adiponectin gene polymorphism and metabolic syndrome incidence and its relationship with the degree of atherosclerosis in patients

机译:脂联素基因多态性与代谢综合征发生率的相关性及其与动脉粥样硬化程度的关系分析

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摘要

The aim of the present study was to determine the correlation between adiponectin (APN) gene polymorphism, metabolic syndrome incidence, and degree of atherosclerosis in patients with this disease. The study was conducted on 369 unrelated patients, diagnosed with metabolic abnormalities. The patients were divided into the metabolic syndrome group (MS group, n=182), the metabolic abnormality group (n=187) and the control group with metabolic normality (n=134), as per the degree of metabolic abnormality. The gene polymorphism of rs121917815 site of APN gene was detected by TaqMAN probe technique, and the OR values of different genotypes and alleles were calculated. The APN protein, C-reactive protein (CRP), IL-1 and high-density lipoprotein (HDL) 2a and 2b expression level changes were detected by immunoblotting. The atherosclerosis index (AI) of each allele in patients with MS was calculated. Compared with the control group, the expression levels of APN protein in the metabolic abnormality and MS groups were significantly decreased. However, there was no distinct difference in the comparison of gene polymorphism between the control and metabolic abnormality groups. The CC genotype frequency and C allele frequency of rs121917815 polymorphic site in the MS group were significantly increased, compared with the control group. The TT genotype frequency and T allele frequency were significantly decreased and the OR values of the CC genotype and C allele were increased. The results of immunoblotting showed that there was no obvious change of CRP, IL-1, HDL-2a and HDL-2b in the three groups, and there was no statistically significant difference in the comparison of AI between the MS and control groups as well as the metabolic abnormality group. The APN gene polymorphic site rs121917815 is associated with MS. The occurrence of CC genotype and C allele increased the incidence of MS, but it did not increase the degree of atherosclerosis in MS patients.
机译:本研究的目的是确定脂联素(APN)基因多态性,代谢综合征发生率和该病患者的动脉粥样硬化程度之间的相关性。这项研究是针对369名无关联的,被诊断患有代谢异常的患者进行的。根据代谢异常程度将患者分为代谢综合征组(MS组,n = 182),代谢异常组(n = 187)和具有代谢正常的对照组(n = 134)。用TaqMAN探针技术检测APN基因rs121917815位点的基因多态性,并计算出不同基因型和等位基因的OR值。通过免疫印迹检测了APN蛋白,C反应蛋白(CRP),IL-1和高密度脂蛋白(HDL)2a和2b表达水平的变化。计算MS患者每个等位基因的动脉粥样硬化指数(AI)。与对照组相比,代谢异常组和MS组APN蛋白的表达水平明显降低。但是,对照组和代谢异常组之间的基因多态性比较没有明显差异。与对照组相比,MS组rs121917815多态性位点的CC基因型频率和C等位基因频率显着增加。 TT基因型频率和T等位基因频率显着降低,CC基因型和C等位基因的OR值升高。免疫印迹结果显示,三组的CRP,IL-1,HDL-2a和HDL-2b均无明显变化,MS与对照组之间AI的比较也无统计学意义。作为代谢异常组。 APN基因多态性位点rs121917815与MS相关。 CC基因型和C等位基因的出现增加了MS的发生率,但并未增加MS患者的动脉粥样硬化程度。

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