探讨急性心肌梗死合并阿尔茨海默病的发病机制及关键基因。

Exploring the pathogenesis and key genes associated of acute myocardial infarction complicated with Alzheimer's disease.

机构信息

Department of Cardiology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.

Department of Medical Image Science, Liaoning Cancer Hospital, Shenyang, Liaoning, China.

出版信息

Sci Rep. 2024 Jan 16;14(1):1449. doi: 10.1038/s41598-024-52094-4.

Abstract

Despite mounting evidence linking Acute Myocardial Infarction (AMI) to Alzheimer's disease (AD), the shared mechanism of these two conditions' occurrence remains unclear. This research aims to delve deeper into the molecular process of the occurrence of the two diseases. We retrieved the gene expression profiles of AD (GSE5281) and AMI (GSE66360) from the Gene Expression Omnibus database. Then, a total of 22 common differentially expressed genes (DEGs) including one downregulated gene and 21 upregulated genes were chosen for further analysis. Following the discovery of the common DEGs between AMI and AD, we performed protein-protein interaction analysis and hub gene identification analysis. Next, ten important hub genes were identified. Additionally, the key genes were identified by the least absolute shrinkage and selection operator and support vector machine-recursive feature elimination and multivariable logistic regression analysis. The BCL6 was identified to be the most connected with AMI and AD. Finally, the BCL6 gene was validated in the GSE40680 (AMI) and GSE122063 (AD) datasets. Our research indicates that AMI and AD share a comparable pathophysiology. The Hub genes, especially BCL6, were essential in developing AMI and AD. In addition, these hub genes and shared pathways can offer fresh perspectives for additional mechanism investigation.

摘要

尽管越来越多的证据将急性心肌梗死 (AMI) 与阿尔茨海默病 (AD) 联系起来,但这两种疾病发生的共同机制仍不清楚。本研究旨在更深入地研究这两种疾病发生的分子过程。我们从基因表达综合数据库中检索了 AD(GSE5281)和 AMI(GSE66360)的基因表达谱。然后,选择了总共 22 个常见的差异表达基因 (DEG),包括一个下调基因和 21 个上调基因进行进一步分析。在发现 AMI 和 AD 之间的共同 DEG 后,我们进行了蛋白质-蛋白质相互作用分析和枢纽基因识别分析。接下来,确定了 10 个重要的枢纽基因。此外,通过最小绝对收缩和选择算子和支持向量机递归特征消除以及多变量逻辑回归分析确定了关键基因。BCL6 被确定与 AMI 和 AD 最相关。最后,在 GSE40680(AMI)和 GSE122063(AD)数据集验证了 BCL6 基因。我们的研究表明,AMI 和 AD 具有相似的病理生理学。Hub 基因,特别是 BCL6,在 AMI 和 AD 的发生中起着重要作用。此外,这些枢纽基因和共享途径可以为进一步的机制研究提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fba/10791667/bce2af4541c2/41598_2024_52094_Fig1_HTML.jpg

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