The effect of dapagliflozin on anemia in elderly patients with heart failure by bioinformatics analysis

Insights

Dapagliflozin may impact anemia in elderly heart failure patients by targeting key genes like AKT1. This bioinformatics study identified 134 target genes and potential pathways, offering new insights into treatment strategies.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacogenomics
  • Bioinformatics

Background:

  • Anemia is common in heart failure patients, worsening symptoms.
  • Dapagliflozin, an SGLT-2 inhibitor, shows cardiovascular benefits.
  • The effect of dapagliflozin on anemia in elderly heart failure patients remains unclear.

Purpose of the Study:

  • To investigate the effect of dapagliflozin on anemia in elderly patients with heart failure using bioinformatics.
  • To identify potential molecular targets and pathways involved in this interaction.

Main Methods:

  • Bioinformatics analysis to determine dapagliflozin target genes.
  • Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis.
  • Construction of protein-protein interaction (PPI) networks and molecular docking simulations.

Main Results:

  • Identified 134 target genes for dapagliflozin in heart failure-associated anemia.
  • Key pathways implicated include lipid metabolism, AGE-RAGE signaling, and insulin signaling.
  • Hub genes identified: AKT1, TP53, GAPDH, TNF, CASP3, EGFR, and MAPK3.
  • Molecular docking confirmed interaction between dapagliflozin and AKT1.

Conclusions:

  • Dapagliflozin's effect on anemia in elderly heart failure patients involves multiple molecular pathways.
  • Hub genes like AKT1 are critical targets for dapagliflozin's action.
  • Further research is warranted to validate these findings and explore therapeutic potential.
Abstract

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