首页> 外文期刊>Journal of clinical laboratory analysis. >LncRNA ANRIL/miR‐125a axis exhibits potential as a biomarker for disease exacerbation, severity, and inflammation in bronchial asthma
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LncRNA ANRIL/miR‐125a axis exhibits potential as a biomarker for disease exacerbation, severity, and inflammation in bronchial asthma

机译:LNCRNA ANRIL / MIR-125A轴表现为疾病加剧,严重程度和支气管哮喘炎症的潜力

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Background This study aimed to explore the correlation of lncRNA ANRIL/miR‐125a axis with disease risk, severity, and inflammatory cytokines of bronchial asthma. Methods Plasma samples from 90 patients with bronchial asthma at exacerbation (BA‐E), 90 with bronchial asthma at remission (BA‐R), and 90 controls (healthy subjects) were collected. The qPCR was used for lncRNA ANRIL and miR‐125a detection, and ELISA was adopted for pro‐inflammatory cytokines detection. Participants’ characteristics, laboratory tests, and the pulmonary ventilation function examinations were recorded. Results LncRNA ANRIL was negatively correlated with miR‐125a in BA‐E patients, BA‐R patients, and controls. LncRNA ANRIL/miR‐125a axis was upregulated in BA‐E patients compared with BA‐R patients and controls. ROC curve analyses illuminated that lncRNA ANRIL/miR‐125a axis was of good value in distinguishing BA‐E patients from BA‐R patients and controls. As to pulmonary ventilation functions, lncRNA ANRIL/miR‐125a axis was negatively associated with FEV 1 /FVC and FEV 1 %predicted in bronchial asthma patients, especially in BA‐E patients. Regarding inflammation, lncRNA ANRIL/miR‐125a axis was positively correlated with pro‐inflammatory cytokines in bronchial asthma patients, especially in BA‐E patients. In addition, lncRNA ANRIL/miR‐125a axis was positively correlated with exacerbation severity in BA‐E patients. Conclusion LncRNA ANRIL/miR‐125a is potentially indicative of disease exacerbation, exacerbation severity, and inflammation for bronchial asthma, while these findings are preliminary and need further confirmation.
机译:背景技术本研究旨在探讨LNCRNA anriL / miR-125a轴与支气管哮喘的疾病风险,严重程度和炎症细胞因子的相关性。方法收集来自缓解(Ba-E)的90例支气管哮喘患者的血浆样品,缓解(Ba-R)和90种对照(健康受试者)的支气管哮喘。 QPCR用于LNCRNA anril和miR-125a检测,并采用ELISA进行促炎细胞因子检测。参与者的特征,实验室测试和肺通气功能检查被记录出来。结果LNCRNA anril与BA-E患者的miR-125a呈负相关,Ba-R患者和对照。与BA-R患者和对照相比,在BA-E患者中,在BA-E患者中上调LNCRNA anril / miR-125a轴。 ROC曲线分析照亮了LNCRNA ANRIL / MIR-125A轴在区分BA-R患者和对照的患者中具有良好的价值。对于肺通气功能,LNCRNA anril / miR-125a轴与支气管哮喘患者的支气管哮喘患者预测的FEV 1 / FVC和FEV 1%负相关,特别是在BA-E患者中。关于炎症,LNCRNA anriL / miR-125a轴与支气管哮喘患者的促炎细胞因子呈正相关,特别是在BA-E患者中。此外,LNCRNA anriL / miR-125a轴与Ba-E患者的恶化严重程度正相关。结论LNCRNA anril / miR-125a可能指示支气管哮喘的疾病恶化,恶化严重程度和炎症,而这些发现是初步的并且需要进一步确认。

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