Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis.
dc.contributor.author | Crespo-Facorro, Benedicto | |
dc.contributor.author | Ruiz-Veguilla, Miguel | |
dc.contributor.author | Vazquez-Bourgon, Javier | |
dc.contributor.author | Sanchez-Hidalgo, Ana C | |
dc.contributor.author | Garrido-Torres, Nathalia | |
dc.contributor.author | Cisneros, Jose M | |
dc.contributor.author | Prieto, Carlos | |
dc.contributor.author | Sainz, Jesus | |
dc.contributor.funder | MINECO | |
dc.contributor.funder | FEDER | |
dc.date.accessioned | 2025-01-07T15:46:25Z | |
dc.date.available | 2025-01-07T15:46:25Z | |
dc.date.issued | 2021-03-02 | |
dc.description.abstract | 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 nonaffective 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 | |
dc.description.version | Si | |
dc.identifier.citation | Crespo-Facorro B, Ruiz-Veguilla M, Vázquez-Bourgon J, Sánchez-Hidalgo AC, Garrido-Torres N, Cisneros JM, et al. Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis. Front Pharmacol. 2021 Mar 2;12:646701. | |
dc.identifier.doi | 10.3389/fphar.2021.646701 | |
dc.identifier.issn | 1663-9812 | |
dc.identifier.pmc | PMC7982825 | |
dc.identifier.pmid | 33762960 | |
dc.identifier.pubmedURL | https://pmc.ncbi.nlm.nih.gov/articles/PMC7982825/pdf | |
dc.identifier.unpaywallURL | https://www.frontiersin.org/articles/10.3389/fphar.2021.646701/pdf | |
dc.identifier.uri | https://hdl.handle.net/10668/27392 | |
dc.journal.title | Frontiers in pharmacology | |
dc.journal.titleabbreviation | Front Pharmacol | |
dc.language.iso | en | |
dc.organization | SAS - Hospital Universitario Virgen del Rocío | |
dc.organization | Instituto de Investigación Biomédica de Sevilla (IBIS) | |
dc.page.number | 8 | |
dc.provenance | Realizada la curación de contenido 13/03/2025 | |
dc.publisher | Frontiers Research Foundation | |
dc.pubmedtype | Journal Article | |
dc.relation.projectID | SAF2016-76046-R | |
dc.relation.projectID | SAF2013-46292-R | |
dc.relation.publisherversion | https://doi.org/10.3389/fphar.2021.646701 | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | SARS-CoV-2 | |
dc.subject | coronavirus | |
dc.subject | elopiprazole | |
dc.subject | immunology | |
dc.subject | inflammation | |
dc.subject | psychosis | |
dc.subject | repurposing drugs | |
dc.subject.decs | Pacientes | |
dc.subject.decs | Terapéutica | |
dc.subject.decs | Trastornos psicóticos | |
dc.subject.decs | Estándares de referencia | |
dc.subject.decs | Patología | |
dc.subject.decs | Inmunidad | |
dc.subject.decs | Enzimas | |
dc.subject.decs | Enfermedades inflamatorias del intestino | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Antipsychotic Agents | |
dc.subject.mesh | phenylpiperazine | |
dc.subject.mesh | Transcriptome | |
dc.subject.mesh | Drug Repositioning | |
dc.subject.mesh | Gene Expression Profiling | |
dc.subject.mesh | Immunity | |
dc.subject.mesh | Psychotic Disorders | |
dc.subject.mesh | Signal Transduction | |
dc.subject.mesh | Receptors, Antigen, B-Cell | |
dc.title | Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 12 |