Key result
Bioinformatic analysis of myocardial tissue before and after LVAD implantation identified 37 differentially expressed genes, revealing a marked increase in neutrophil degranulation signaling and chemokine-mediated leukocyte chemotaxis.
Why the study?
The study was conducted to clarify changes in myocardial gene expression profiles following left ventricular assist device (LVAD) implantation and their molecular biological significance.
What are the changes in myocardial gene expression profiles and related molecular pathways after LVAD implantation?
What are the changes in myocardial gene expression profiles and related molecular pathways after LVAD implantation?
p-value: p=<0.05
Bioinformatic analysis reveals that inflammatory signaling pathways, particularly chemokine-mediated leukocyte chemotaxis via GPCR-ligand binding, play a crucial role in myocardial tissue remodeling after LVAD implantation.
Objective: The aim of this study was to clarify the changes of myocardial gene expression profile after left ventricular assist device (LVAD) implantation and the related molecular biological significance. Methods: A thorough bioinformatic analysis to evaluate the changes in gene expression profile in patients pre-LVAD and post-LVAD was conducted. Four relevant gene expression datasets-GSE430, GSE974, GSE21610, and GSE52601 from Gene Expression Omnibus (GEO) database were downloaded. Analysis of GEO2R, Gene Ontology (GO), protein-protein interaction (PPI) were used to determine differentially expressed genes (DEGs) and their function, respectively. Results: A total of 37 DEGs were identified, including 26 down-regulated and 11 up-regulated genes. The molecular function of DEGs were enriched in "cytokine activity," "neurotransmitter binding," "receptor ligand activity." The gene set enrichment analysis (GSEA) revealed an overall marked increase of neutrophil degranulation signaling, closely correlated with the G protein coupled receptor (GPCR)-ligand binding process after LVAD assistance. 16 hubgenes in these DEGs were further selected and the biological process involved is mainly related to positive regulation of leukocyte chemotaxis mediated by chemokines. Conclusion: Inflammatory signaling pathway is crucial for the pathophysiology after LVAD implantation. Chemokines mediate cardiac inflammatory response and tissue remodeling after LVAD implantation through GPCR-ligand binding.
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Ajmal et al. (2022) studied Heart failure with reduced ejection fraction (HFrEF) (n=81). Left ventricular assist device (LVAD) vs. Pre-LVAD baseline and non-failing control hearts was evaluated on Differentially expressed genes (DEGs) in myocardial tissue pre- and post-LVAD (p=<0.05). Bioinformatic analysis of myocardial tissue before and after LVAD implantation identified 37 differentially expressed genes, revealing a marked increase in neutrophil degranulation signaling and chemokine-mediated leukocyte chemotaxis.
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