Your browser doesn't support javascript.
loading
S100A9 and SOCS3 as diagnostic biomarkers of acute myocardial infarction and their association with immune infiltration.
Lin, Ze-Liang; Liu, Yan-Cun; Gao, Yu-Lei; Chen, Xin-Sen; Wang, Chao-Lan; Shou, Song-Tao; Chai, Yan-Fen.
Afiliação
  • Lin ZL; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Liu YC; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Gao YL; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Chen XS; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Wang CL; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Shou ST; Department of Emergency Medicine, Tianjin Medical University General Hospital.
  • Chai YF; Department of Emergency Medicine, Tianjin Medical University General Hospital.
Genes Genet Syst ; 97(2): 67-79, 2022 Jul 16.
Article em En | MEDLINE | ID: mdl-35675985
ABSTRACT
Acute myocardial infarction (AMI) is one of the leading causes of death globally, with a mortality rate of over 20%. However, the diagnostic biomarkers frequently used in current clinical practice have limitations in both sensitivity and specificity, likely resulting in delayed diagnosis. This study aimed to identify potential diagnostic biomarkers for AMI and explored the possible mechanisms involved. Datasets were retrieved from the Gene Expression Omnibus. First, we identified differentially expressed genes (DEGs) and preserved modules, from which we identified candidate genes by LASSO (least absolute shrinkage and selection operator) regression and the SVM-RFE (support vector machine-recursive feature elimination) algorithm. Subsequently, we used ROC (receiver operating characteristic) analysis to evaluate the diagnostic accuracy of the candidate genes. Thereafter, functional enrichment analysis and an analysis of immune infiltration were implemented. Finally, we assessed the association between biomarkers and biological processes, infiltrated cells, clinical traits, tissues and time points. We identified nine preserved modules containing 1,016 DEGs and managed to construct a diagnostic model with high accuracy (GSE48060 AUC = 0.923; GSE66360 AUC = 0.973) incorporating two genes named S100A9 and SOCS3. Functional analysis revealed the pivotal role of inflammation; immune infiltration analysis indicated that eight cell types (monocytes, epithelial cells, neutrophils, CD8+ T cells, Th2 cells, NK cells, NKT cells and platelets) were likely involved in AMI. Furthermore, we observed that S100A9 and SOCS3 were correlated with inflammation, variably infiltrated cells, clinical traits of patients, sampling tissues and sampling time points. In conclusion, we suggested S100A9 and SOCS3 as diagnostic biomarkers of AMI and discovered their association with inflammation, infiltrated immune cells and other factors.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Calgranulina B / Proteína 3 Supressora da Sinalização de Citocinas / Infarto do Miocárdio Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Genes Genet Syst Assunto da revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Calgranulina B / Proteína 3 Supressora da Sinalização de Citocinas / Infarto do Miocárdio Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Genes Genet Syst Assunto da revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Ano de publicação: 2022 Tipo de documento: Article