机构地区:[1]川北医学院附属医院高尿酸血症与痛风研究中心,南充637000 [2]川北医学院附属医院风湿免疫科,南充637000 [3]川北医学院附属医院老年科,南充637000 [4]遂宁市第三人民医院急诊科,遂宁629000
出 处:《中华风湿病学杂志》2024年第5期303-311,共9页Chinese Journal of Rheumatology
基 金:国家自然科学基金面上项目(81974250);四川省南充市科技项目(20SXQT0308,20SX-CXTD0002);川北医学院附属医院科研项目(2022ZD003)。
摘 要:目的探索长链非编码RNA(lncRNA)结直肠肿瘤差异表达基因(CRNDE)、微RNA-181a-5p(miR-181a-5p)、自噬相关蛋白5(ATG5)在原发性痛风性关节炎(GA)患者外周血中的表达及临床意义。方法收集80例GA患者[急性期痛风(AG)、间歇期痛风(IG)各40例]和50名健康体检者(HC)临床资料、实验室检查指标及外周血标本。采用实时荧光定量PCR(RT-qPCR)检测lncRNA CRNDE、miR-181a-5p、ATG5 mRNA表达水平;蛋白质印迹法检测ATG5蛋白表达水平。比较3组间lncRNA CRNDE、miR-181a-5p、ATG5 mRNA表达量并与临床指标做相关性分析,构建受试者工作特征曲线(ROC)评估lncRNA CRNDE、miR-181a-5p、ATG5 mRNA在痛风诊断中的价值。符合正态分布的计量资料使用t检验或方差分析,非正态分布用Mann-Whitney U检验或Kruskal-Wallis H检验,变量间的相关分析采用Spearman分析,各指标的诊断价值采用ROC曲线。结果①LncRNA CRNDE、miR-181a-5p、ATG5 mRNA在3组间表达差异均有统计学意义(H=32.12、57.73、68.32,P均<0.001)。其中,lncRNA CRNDE表达水平在AG组明显高于IG组和健康对照组[61.95(11.39,108.30)×10^(-3),25.71(15.40,38.40)×10^(-3),13.80(3.97,23.99)×10^(-3);Z=-3.24,P=0.001;Z=-5.03,P<0.001],且在IG组的表达水平高于健康对照组(Z=-3.56,P<0.001);miR-181a-5p、ATG5 mRNA表达水平在AG组明显低于IG组及健康对照组[miR-181a-5p:39.81(31.22,69.38)×10^(-3),60.74(44.19,90.35)×10^(-3),121.30(101.50,316.90)×10^(-3);Z=-3.01,P=0.030;Z=-6.93,P<0.001。ATG5 mRNA:4.52(2.31,26.63)×10^(-3),43.63(13.72,102.70)×10^(-3),153.90(66.62,365.80)×10^(-3);Z=-5.47、-7.36,P均<0.001],在IG组的表达水平低于健康对照组(Z=-5.25、-4.47,P均<0.001)。ATG5蛋白表达水平在3组间表达的差异有统计学意义(F=6.24,P=0.030),AG组高于健康对照组,差异有统计学意义[(0.96±0.13)与(0.61±0.04),t=4.25,P=0.013],但IG组(0.78±0.15)与AG组(t=1.51,P=0.206)、HC组(t=1.85,P=0.138)差异无统计学意义。②Spearman相关性分析显示,在GA�Objective To explore the expression and clinical significance of long non-coding RNA colorectal neoplasia differentially expressed(lncRNA CRNDE),microRNA-181a-5p(miR-181a-5p)and autophagy related 5(ATG5)in the peripheral blood of patients with gouty arthritis(GA)patients.Methods The clinical data,laboratory parameters and peripheral blood samples were collected from 40 patients with acute gout(AG),40 patients with intermittent gout(IG)and 50 healthy subjects(HC).The expression levels of lncRNA CRNDE,miR-181a-5p and ATG5 mRNA were detected by real-time fluorescence quantification(RT-qPCR)and the expression level of ATG5 protein was detected by Western-blot.The expression levels of lncRNA CRNDE,miR-181a-5p,ATG5 mRNA were compared among the three groups and correlated with clinical indices,and a subject operating characteristic curve(ROC)was constructed to assess the value of lncRNA CRNDE,miR-181a-5p,ATG5 mRNA in the diagnosis of gout.Measurements conforming to normal distribution were analyzed using t test or ANOVA,data with non-normal distribution was analyzed using Mann-Whitney U test or Kruskal-Wallis H test,correlation analysis between variables was analyzed using Spearman's analysis,and the diagnostic value of each indicator was analyzed using ROC curve.Results①The differences in the expression of lncRNA CRNDE,miR-181a-5p,and ATG5 mRNA between the three groups were statistically significant(H=32.12,57.73,68.32,all P<0.001).Among them,lncRNA CRNDE expression level in the AG group was significantly higher than that in the IG group and healthy control group[61.95(11.39,108.30)×10^(-3),25.71(15.40,38.40)×10^(-3),13.80(3.97,23.99)×10^(-3);Z=-3.24,P=0.001;Z=-5.03,P<0.001],and the expression level of IG group was higher than that of healthy control group(Z=-3.56,P<0.001);miR-181a-5p and ATG5 mRNA expression levels in AG group were significantly lower than those in IG group and healthy control group[miR-181a-5p:39.81(31.22,69.38)×10^(-3),60.74(44.19,90.35)×10^(-3),121.30(101.50,316.90)×10^(-3);Z=-3.01,P=0.030;
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