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Correlation of interleukin-6 572C/G gene polymorphism with airway inflammation and remodeling in patients with COPD

机译:白细胞介素-6 572C / G基因多态性与COPD患者气道炎症和重塑的相关性

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Objective: To study the correlation of interleukin-6 (IL-6) 572C/G gene polymorphism with airway inflammation and remodeling in patients with COPD. Methods: Patients with stable COPD who were treated in Hanzhong Central Hospital between March 2015 and December 2017 were selected and enrolled in the COPD group of the study, and healthy volunteers who received physical examination in Hanzhong Central Hospital during the same period and had general information matched with that of patients with COPD were selected as the control group. The peripheral blood was collected to detect the IL-6 gene 572 C/G locus polymorphism, and the serum was collected to detect the levels of inflammatory response mediators and airway remodeling indexes. Results: The proportion of GG genotype in COPD group was higher than that in control group, and the proportion of GC+CC genotype was lower than that in control group; serum IL-6, IL-21, IFN-γ, CXCL13, CTRP4, CTRP5, TGF-β1, VEGF, MMP2 and NE levels of COPD group were significantly higher than those of control group whereas α1-AT and TIMP1 levels were significantly lower than those of control group, and serum IL-6, IL-21, IFN-γ, CXCL13, CTRP4, CTRP5, TGF-β1, VEGF, MMP2 and NE levels of COPD patients with GG genotype were higher than those of COPD patients with GC+CC genotype whereas α1-AT and TIMP1 levels were lower than those of COPD patients with GC+CC genotype. Conclusion: The mutation from IL-6 gene 572C/G locus allele C to G can aggravate the inflammatory response and airway remodeling in the course of COPD.
机译:目的:探讨白细胞介素6(IL-6)572C / G基因多态性与COPD患者气道炎症和重塑的相关性。方法:选择2015年3月至2017年12月在汉中市中心医院接受治疗的稳定COPD患者,并纳入该研究的COPD组,同时在汉中市中心医院接受身体检查并具有一般信息的健康志愿者选择与COPD患者相匹配的作为对照组。收集外周血以检测IL-6基因572 C / G基因座多态性,并收集血清以检测炎症反应介质的水平和气道重塑指数。结果:COPD组GG基因型比例高于对照组,GC + CC基因型比例低于对照组。 COPD组的血清IL-6,IL-21,IFN-γ,CXCL13,CTRP4,CTRP5,TGF-β1,VEGF,MMP2和NE水平显着高于对照组,而α1-AT和TIMP1水平则显着降低GG基因型的COPD患者的血清IL-6,IL-21,IFN-γ,CXCL13,CTRP4,CTRP5,TGF-β1,VEGF,MMP2和NE的水平均高于对照组。 GC + CC基因型,而α1-AT和TIMP1水平低于GC + CC基因型的COPD患者。结论:IL-6基因572C / G基因座等位基因C向G的突变可加重COPD过程中的炎症反应和气道重塑。

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