Department of Respiratory and Critical Care Medicine, The First People's Hospital of Wenling, Taizhou, Zhejiang 317500, China.
Department of Integrated Traditional and Western Medicine, The First People's Hospital of Wenling, Taizhou, Zhejiang 317500, China.
Contrast Media Mol Imaging. 2021 Dec 14;2021:9731502. doi: 10.1155/2021/9731502. eCollection 2021.
The expression profile and image observation of miRNA in serum of patients with obstructive sleep apnea-hypopnea syndrome were investigated. Bioinformatics methods were used to explore the molecular mechanism of obstructive sleep apnea-hypopnea syndrome (OSAHS)-related hypertension and explore the differentially expressed core miRNAs and regulatory factors, providing a theoretical basis for seeking molecular targets for clinical diagnosis and treatment. The miRNA datasets of patients with OSAHS and those with hypertension were downloaded from the public database to obtain differentially expressed miRNAs and explore the biological processes and pathways involved in the target genes. The core miRNAs and competitive endogenous RNA (ceRNA) transcription factors (TFs) were obtained by database mining and Cytoscape network analysis. The results showed that 2,579 differentially expressed miRNAs were obtained from the GSE112093 dataset. Seven upregulated miRNAs (hsa-miR-7107-5p, hsa-miR-7110-5p, hsa-miR-595, hsa-miR-1268b, hsa-miR-3064-5p, hsa-miR-68565p, and hsa-miR-1180-3p) and one downregulated miRNA (hsa-miR-22-3p) were obtained from the GSE112093 dataset. It is proved that hsa-miR-22-3p, hsa-miR-595, hsa-miR-6856-5pKcnq1ot1, neat1, Tsix, ERG, kdm2b, and Runx1 may be involved in the pathogenesis of OSAHS-related hypertension, which provided a theoretical basis for the mechanism research and clinical treatment of OSAHS.
研究了阻塞性睡眠呼吸暂停低通气综合征(OSAHS)患者血清中 miRNA 的表达谱和图像观察。采用生物信息学方法探讨了阻塞性睡眠呼吸暂停低通气综合征(OSAHS)相关高血压的分子机制,探讨了差异表达的核心 miRNA 和调节因子,为寻找临床诊断和治疗的分子靶点提供了理论依据。从公共数据库中下载 OSAHS 患者和高血压患者的 miRNA 数据集,获得差异表达的 miRNA,并探讨其靶基因涉及的生物学过程和途径。通过数据库挖掘和 Cytoscape 网络分析获得核心 miRNA 和竞争内源性 RNA(ceRNA)转录因子(TFs)。结果从 GSE112093 数据集获得了 2579 个差异表达的 miRNA。从 GSE112093 数据集获得了 7 个上调的 miRNA(hsa-miR-7107-5p、hsa-miR-7110-5p、hsa-miR-595、hsa-miR-1268b、hsa-miR-3064-5p、hsa-miR-68565p 和 hsa-miR-1180-3p)和 1 个下调的 miRNA(hsa-miR-22-3p)。证明 hsa-miR-22-3p、hsa-miR-595、hsa-miR-6856-5p、Kcnq1ot1、neat1、Tsix、ERG、kdm2b 和 Runx1 可能参与了 OSAHS 相关高血压的发病机制,为 OSAHS 的机制研究和临床治疗提供了理论依据。