Yao Yuqian, Zhao Hemeng, Zhu Xiaoyu, Fang Yafei, Feng Yue
The First People's Hospital of Lianyungang & Xuzhou Medical University Affiliated Hospital of Lianyungang & The First Affiliated Hospital of Kangda College of Nanjing Medical University, Department of Pediatric Internal Medicine, Lianyungangk, People's Republic of China.
J Med Biochem. 2025 Aug 21;44(5):1118-1126. doi: 10.5937/jomb0-52498.
To guide clinical doctors, current work has been designed to explore the abnormal expressions of miRNAs in plasma samples of patients with immune thrombocytopenic purpura (ITP).
Bioinformatic analysis was performed using the GSE80401 chip. The study subjects were recruited from the First People's Hospital of Lianyungang between May 2021 and December 2023. 48 ITP patients admitted to the intensive care unit were enrolled. miRNA levels were examined using real-time polymerase chain reaction. All data were analysed using SPSS 22.0 software. The potential diagnosis value of the significantly up-regulated and down-regulated miRNAs was evaluated using a receiver operator characteristic (ROC) curve.
We performed bioinformatical analysis on the GSE80401 chip and identified the differently expressed miRNAs in ITP patients compared to the controls, and the results of the heat map showed the results. GO and pathway analysis revealed the process that involved the differently expressed miRNAs. Next, the results of RT-qPCR analysis showed the levels of miR-877-3p, miR-425-3p, miR-122-5p, miR-1281, and miR-1825 were significantly increased. In contrast, the miR-3945, miR-4430, miR-3158-5p, miR-3131, and miR-4655-3p levels were markedly decreased in plasma samples of ITP patients compared with the controls. Finally, results showed that the area under the ROC curve of miRNAs was as follows: miR-877-3p, 0.9349, miR-425-3p, 0.8607, miR-1281, 0.7131, miR-1825, 0.8928, miR-3945, 0.8459, miR-4430, 0.8112, miR-3158-5p, 0.6059, miR-3131, 0.8989, suggesting that the above miRNAs may serve as biomarkers for distinguishing the ITP patients from healthy controls.
miRNAs may have predictive value for the diagnosis of ITP. The results of current work may provide new clues for the pathogenesis of ITP, which in turn offers a new theoretical basis and therapeutic tools for the clinical diagnosis and treatment of ITP.
为指导临床医生,目前已开展相关工作,旨在探究免疫性血小板减少性紫癜(ITP)患者血浆样本中微小RNA(miRNA)的异常表达情况。
使用GSE80401芯片进行生物信息学分析。研究对象于2021年5月至2023年12月期间从连云港市第一人民医院招募。纳入48例入住重症监护病房的ITP患者。采用实时聚合酶链反应检测miRNA水平。所有数据均使用SPSS 22.0软件进行分析。使用受试者工作特征(ROC)曲线评估显著上调和下调的miRNA的潜在诊断价值。
我们对GSE80401芯片进行了生物信息学分析,确定了ITP患者与对照组相比差异表达的miRNA,热图结果显示了相关情况。基因本体(GO)和通路分析揭示了涉及差异表达miRNA的过程。接下来,逆转录-定量聚合酶链反应(RT-qPCR)分析结果显示,miR-877-3p、miR-425-3p、miR-122-5p、miR-1281和miR-1825的水平显著升高。相比之下,与对照组相比,ITP患者血浆样本中miR-3945、miR-4430、miR-3158-5p、miR-3131和miR-4655-3p的水平明显降低。最后,结果显示miRNA的ROC曲线下面积如下:miR-877-3p为0.9349,miR-425-3p为0.8607,miR-1281为0.7131,miR-1825为0.8928,miR-3945为0.8459,miR-4430为0.8112,miR-3158-5p为0.6059,miR-3131为0.8989,这表明上述miRNA可能作为区分ITP患者与健康对照的生物标志物。
miRNA可能对ITP的诊断具有预测价值。当前研究结果可能为ITP的发病机制提供新线索,进而为ITP的临床诊断和治疗提供新的理论基础和治疗工具。