Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12323/6102
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dc.contributor.authorFico, Giovanna-
dc.contributor.authorIsayeva, Ulker-
dc.contributor.authorPrisco, Michele De-
dc.contributor.authorOliva, Vincenzo-
dc.contributor.authorSole, Brisa-
dc.contributor.authorMontejo, Laura-
dc.contributor.authorGrande, Iria-
dc.contributor.authorArbelo, Nestor-
dc.contributor.authorGomez-Ramiro, Marta-
dc.contributor.authorPintor, Luis-
dc.contributor.authorCarpiniello, Bernardo-
dc.contributor.authorManchia, Mirko-
dc.contributor.authorVieta, Eduard-
dc.contributor.authorMurru, Andrea-
dc.date.accessioned2022-10-28T06:07:03Z-
dc.date.available2022-10-28T06:07:03Z-
dc.date.issued2022-10-09-
dc.identifier.citationEuropean Neuropsychopharmacologyen_US
dc.identifier.urihttp://hdl.handle.net/20.500.12323/6102-
dc.description.abstractSeveral psychotropic drugs, including antidepressants (AD), mood stabilizers, and antipsychotics (AP) have been suggested to have favorable effects in the treatment of COVID-19. The aim of this systematic review and meta-analysis was to collect evidence from studies concerning the scientific evidence for the repurposing of psychotropic drugs in COVID-19 treatment. Two independent authors searched PubMed-MEDLINE, Scopus, PsycINFO, and ClinicalTrials.gov databases, and reviewed the reference lists of articles for eligible articles published up to 13th December, 2021. All computational, preclinical and clinical (observational and/or RCTs) studies on the effect of any psychotropic drug on Sars-CoV-2 or patients with COVID-19 were considered for inclusion. We conducted random effect meta-analyses on clinical studies reporting the effect of AD or AP on COVID-19 outcomes. 29 studies were included in the synthesis: 15 clinical, 9 preclinical, and 5 computational studies. 9 clinical studies could be included in the quantitative analyses. AD did not increase the risk of severe COVID-19 (RR= 1.71; CI 0.65-4.51) or mortality (RR=0.94; CI 0.81-1.09). Fluvoxamine was associated with a reduced risk of mortality for COVID-19 (OR=0.15; CI 0.02-0.95). AP increased the risk of severe COVID-19 (RR=3.66; CI 2.76-4.85) and mortality (OR=1.53; CI 1.15-2.03). Fluvoxamine might be a possible candidate for psychotropic drug repurposing in COVID-19 due to its anti-inflammatory and antiviral potential, while evidence on other AD is still controversial. Although AP are associated with worse COVID-19 outcomes, their use should be evaluated case to case and ongoing treatment with antipsychotics should be not discontinued in psychiatric patients.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V. and ECNPen_US
dc.subjectCovid-19en_US
dc.subjectpsychotropic drugsen_US
dc.subjectantidepressantsen_US
dc.subjectantipsychoticsen_US
dc.subjectanti-inflammatoryen_US
dc.subjectantiviralen_US
dc.titlePsychotropic drug repurposing for COVID-19: a Systematic Review and Meta-Analysisen_US
dc.typeArticleen_US
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