Key result
Bioinformatics analysis identified 74 differentially expressed genes common to type 1 diabetes and acute myocardial infarction, with STAT3, ITGAM, MMP9, ERBB2, and MAPK3 among the top hub genes.
Why the study?
The pathogenesis common to type 1 diabetes mellitus and acute myocardial infarction remains unclear.
The identification of 10 central genes common to T1D and AMI provides potential novel biomarkers for precision diagnosis and future therapeutic targets.
These genes may inform future biomarkers in T1D-AMI; hypothesis-generating and requires prospective validation before clinical use.
Although the pathogenesis of type 1 diabetes mellitus (T1D) and acute myocardial infarction (AMI) remains unclear. We investigated the key genes and signaling pathways common to T1D and AMI. First, we screened differentially expressed genes (DEGs) co-expressed by T1D and AMI through gene expression synthesis (GEO) database and text mining. David database was used for enrichment and functional analysis of selected genes. The interaction between proteins (PPI) was created using STRING and Cytoscape software. MCODE is used for module analysis of PPI network. A total of 74 human genes that met the criteria were found in T1D and AMI. The first 10 central genes include STAT3, ITGAM, MMP9, ERBB2, MAPK3, FOS, MYD88, MAPK1, TFRC and TNFRSF1A.The establishment of the aforementioned key genes might serve as novel biomarkers for precision diagnosis and providing medical treatment for the occurrence of AMI in T1D patients in the future.
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Ou et al. (2021) studied Type 1 Diabetes Mellitus and Acute Myocardial Infarction (n=28). Type 1 diabetes and acute myocardial infarction vs. Normal controls was evaluated on Identification of differentially expressed genes (DEGs) common to T1D and AMI. Bioinformatics analysis identified 74 differentially expressed genes common to type 1 diabetes and acute myocardial infarction, with STAT3, ITGAM, MMP9, ERBB2, and MAPK3 among the top hub genes.
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