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炎症作为心房颤动中风的危险因素:来自微阵列数据分析的数据。

Inflammation as a risk factor for stroke in atrial fibrillation: data from a microarray data analysis.

机构信息

Department of Anesthesiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

J Int Med Res. 2020 May;48(5):300060520921671. doi: 10.1177/0300060520921671.

Abstract

OBJECTIVE

Stroke is a severe complication of atrial fibrillation (AF). We aimed to discover key genes and microRNAs related to stroke risk in patients with AF using bioinformatics analysis.

METHODS

GSE66724 microarray data, including peripheral blood samples from eight patients with AF and stroke and eight patients with AF without stroke, were downloaded from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) between AF patients with and without stroke were identified using the GEO2R online tool. Functional enrichment analysis was performed using the DAVID database. A protein-protein interaction (PPI) network was obtained using the STRING database. MicroRNAs (miRs) targeting these DEGs were obtained from the miRNet database. A miR-DEG network was constructed using Cytoscape software.

RESULTS

We identified 165 DEGs (141 upregulated and 24 downregulated). Enrichment analysis showed enrichment of certain inflammatory processes. The miR-DEG network revealed key genes, including , , , and , and microRNAs, including miR-1, miR-1-3p, miR-21, miR-21-5p, miR-192, miR-192-5p, miR-155, and miR-155-5p.

CONCLUSION

Dysregulation of certain genes and microRNAs involved in inflammation may be associated with a higher risk of stroke in patients with AF. Evaluating these biomarkers could improve prediction, prevention, and treatment of stroke in patients with AF.

摘要

目的

中风是心房颤动(AF)的严重并发症。我们旨在通过生物信息学分析发现 AF 患者中风风险相关的关键基因和 microRNAs。

方法

从基因表达综合数据库(GEO)下载 GSE66724 微阵列数据集,包括 8 例 AF 合并中风患者和 8 例 AF 无中风患者的外周血样本。使用 GEO2R 在线工具鉴定 AF 合并中风与无中风患者间的差异表达基因(DEGs)。使用 DAVID 数据库进行功能富集分析。使用 STRING 数据库获得蛋白质-蛋白质相互作用(PPI)网络。从 miRNet 数据库获得靶向这些 DEGs 的 microRNAs(miRs)。使用 Cytoscape 软件构建 miR-DEG 网络。

结果

我们鉴定出 165 个 DEGs(141 个上调和 24 个下调)。富集分析显示某些炎症过程的富集。miR-DEG 网络揭示了关键基因,包括、、、和、microRNAs,包括 miR-1、miR-1-3p、miR-21、miR-21-5p、miR-192、miR-192-5p、miR-155 和 miR-155-5p。

结论

某些参与炎症的基因和 microRNAs 的失调可能与 AF 患者中风风险增加相关。评估这些生物标志物可改善 AF 患者中风的预测、预防和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/7222654/41a0d2d716d3/10.1177_0300060520921671-fig1.jpg

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