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The association between MCP-1 VEGF polymorphisms and their serum levels in patients with diabetic foot ulcer

机译:糖尿病足溃疡患者MCP-1VEGF基因多态性与血清水平的关系

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摘要

The purpose of the present study was to investigate distribution of monocyte chemoattractant protein-1 (MCP-1) –2518A/G and vascular endothelial growth factor (VEGF) –634G/C polymorphisms in type 2 diabetes melitus patients (T2DM) presenting diabetic foot ulcer (DFU). Additionally, we evaluated the effects of these 2 polymorphisms on serum levels of MCP-1 and VEGF in the study population.Patients diagnosed with T2DM without or with DFU were recruited in the study. The distribution of MCP-1 –2518A/G and VEGF –634G/C polymorphisms was investigated by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Enzyme-linked immunosorbent assay (ELISA) was applied to detect the protein levels of MCP-1 and VEGF. The comparisons of protein levels in DFU patients were performed by student t test according to their genotypes.The frequencies of GG genotype and G allele of MCP-1 –2518A/G was increased in DFU patients, compared with T2DM patients (odds ratio [OR] = 2.60, 95% confidence interval [CI] = 1.23–5.50, P = .011 and OR = 1.72, 95% CI = 1.18–2.50, P = .005, respectively). Moreover, the increased frequency of GG was significantly associated with up-regulated MCP-1 level in DFU patients (P < .001). Analysis for VEGF –634G/C polymorphisms indicated that the prevalence of CC genotype and C allele of the polymorphisms was decreased in DFU patients, compared with T2DM patients (OR = 0.36, 95% CI = 0.17–0.77, P = .008 and OR = 0.63, 95% CI = 0.43–0.91, P = .015, respectively). DFU patients carrying CC genotype had a higher level of VEGF than those with other genotypes (P = .007).MCP-1 –2518A/G and VEGF –634G/C polymorphisms may involve in occurrence and progress of DFU through regulating transcription activity of the genes.
机译:本研究的目的是调查存在糖尿病足的2型糖尿病患者(T2DM)中单核细胞趋化蛋白1(MCP-1)–2518A / G和血管内皮生长因子(VEGF)–634G / C多态性的分布溃疡(DFU)。此外,我们评估了这2个多态性对研究人群血清MCP-1和VEGF的影响。该研究招募了患有T2DM而无DFU的患者。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)研究了MCP-1 –2518A / G和VEGF –634G / C的分布。酶联免疫吸附法(ELISA)用于检测MCP-1和VEGF的蛋白水平。根据学生的基因型,通过学生t检验比较了DFU患者的蛋白质水平。与T2DM患者相比,DFU患者中MCP-1 –2518A / G的GG基因型和G等位基因频率增加(几率[OR ] = 2.60,95%置信区间[CI] = 1.23-5.50,P = .011和OR = 1.72,95%CI = 1.18-2.50,P = .005)。此外,DFU患者中GG频率增加与MCP-1水平上调显着相关(P <.001)。对VEGF –634G / C多态性的分析表明,与T2DM患者相比,DFU患者的CC基因型和C等位基因的患病率降低(OR = 0.36、95%CI = 0.17-0.77,P = .008和OR = 0.63,95%CI = 0.43-0.91,P = .015)。携带CC基因型的DFU患者的VEGF水平高于其他基因型的患者(P = .007)。MCP-1–2518A / G和VEGF –634G / C多态性可能通过调节DFU的转录活性而参与DFU的发生和发展。基因。

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