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首页> 外文期刊>Journal of cardiovascular translational research >Serum miR-92a-3p as a New Potential Biomarker for Diagnosis of Kawasaki Disease with Coronary Artery Lesions
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Serum miR-92a-3p as a New Potential Biomarker for Diagnosis of Kawasaki Disease with Coronary Artery Lesions

机译:血清miR-92a-3p作为诊断川崎病伴冠状动脉病变的新潜在生物标志物

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Recent studies have suggested that serum microRNAs (miRNAs) are novel biomarkers for many cardiovascular diseases, but their role in Kawasaki disease (KD) is still unclear. We demonstrated that serum miR-92a-3p levels were significantly higher in children with KD compared with children with fever and controls (both P < 0.05). When the disease recovered, miR-92a-3p levels returned to those of controls. Clinical and pathological data showed that high levels of miR-92a-3p were significantly associated with coronary artery lesions (CALs). Analysis of the receiver operating characteristic (ROC) curve showed that serum miR-92a-3p had a sensitivity of 81.8 and a specificity of 66.7 for distinguishing KD with CALs from KD without CALs. The area under the curve was 0.816 (P < 0.05, 95 CI 0.669-0.962). Therefore, the miRNA miR-92a-3p may be used as a potential biomarker for diagnosis of KD and KD with coronary artery lesions.
机译:最近的研究表明,血清microRNA(miRNA)是许多心血管疾病的新型生物标志物,但它们在川崎病(KD)中的作用尚不清楚。我们发现,与发热儿童和对照组相比,川崎病患儿的血清miR-92a-3p水平显著升高(P<均为0.05)。当疾病恢复时,miR-92a-3p水平恢复到对照组的水平。临床和病理数据显示,高水平的miR-92a-3p与冠状动脉病变(CAL)显著相关。受试者工作特征(ROC)曲线分析显示,血清miR-92a-3p鉴别川崎病伴CAL和无冠心川崎病的敏感性为81.8%,特异性为66.7%。曲线下面积为0.816(P < 0.05,95%CI 0.669-0.962)。因此,miRNA miR-92a-3p 可作为诊断川崎病和川崎病伴冠状动脉病变的潜在生物标志物。

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