1. Academic Validation
  2. Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis

Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis

  • Front Pharmacol. 2021 Mar 2;12:646701. doi: 10.3389/fphar.2021.646701.
Benedicto Crespo-Facorro 1 2 Miguel Ruiz-Veguilla 1 2 Javier Vázquez-Bourgon 2 3 4 Ana C Sánchez-Hidalgo 2 5 Nathalia Garrido-Torres 1 Jose M Cisneros 6 7 Carlos Prieto 8 Jesus Sainz 9
Affiliations

Affiliations

  • 1 Department of Psychiatry, School of Medicine, University Hospital Virgen del Rocio-IBIS, Sevilla, Spain.
  • 2 Spanish Network for Research in Mental Health (CIBERSAM), Sevilla, Spain.
  • 3 Department of Psychiatry, University Hospital Marques de Valdecilla - Instituto de Investigacion Marques de Valdecilla (IDIVAL), Santander, Spain.
  • 4 Department of Medicine and Psychiatry, School of Medicine, University of Cantabria, Santander, Spain.
  • 5 Seville Biomedical Research Centre (IBiS), Sevilla, Spain.
  • 6 Department of Infectious Diseases, Microbiology and Preventive Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio, University of Seville, Salamanca, Spain.
  • 7 Spanish Network for Research in Infectious Diseases (REIPI), Madrid, Spain.
  • 8 Bioinformatics Service, Nucleus, University of Salamanca, Salamanca, Spain.
  • 9 Spanish National Research Council (CSIC), Institute of Biomedicine and Biotechnology of Cantabria, Santander, Spain.
Abstract

Background: Antipsychotics modulate expression of inflammatory cytokines and inducible inflammatory Enzymes. Elopiprazole (a phenylpiperazine antipsychotic drug in phase 1) has been characterized as a therapeutic drug to treat SARS-CoV-2 Infection in a repurposing study. We aim to investigate the potential effects of aripiprazole (an FDA approved phenylpiperazine) on COVID-19-related immunological parameters. Methods: Differential gene expression profiles of non-COVID-19 vs. COVID-19 RNA-Seq samples (CRA002390 project in GSA database) and drug-naïve patients with non-affective psychosis at baseline and after three months of aripiprazole treatment were identified. An integrative transcriptomic analyses of aripiprazole effects on differentially expressed genes in COVID-19 patients was performed. Findings: 82 out the 377 genes (21.7%) with expression significantly altered by aripiprazole have also their expression altered in COVID-19 patients and in 93.9% of these genes their expression is reverted by aripiprazole. The number of common genes with expression altered in both analyses is significantly higher than expected (Fisher's Exact Test, two tail; p value = 3.2e-11). 11 KEGG pathways were significantly enriched with genes with altered expression both in COVID-19 patients and aripiprazole medicated non-affective psychosis patients (p adj<0.05). The most significant pathways were associated to immune responses and mechanisms of hyperinflammation-driven pathology (i.e.,"inflammatory bowel disease (IBD)" (the most significant pathway with a p adj of 0.00021), "Th1 and Th2 cell differentiation" and "B cell receptor signaling pathway") that have been also associated with COVID19 clinical outcome. Interpretation: This exploratory investigation may provide further support to the notion that a protective effect is exerted by aripiprazole (phenylpiperazine) by modulating the expression of genes that have shown to be altered in COVID-19 patients. Along with many ongoing studies and clinical trials, repurposing available medications could be of use in countering SARS-CoV-2 Infection, but require further studies and trials.

Keywords

SARS-CoV-2; coronavirus; elopiprazole; immunology; inflammation; psychosis; repurposing drugs.

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