Evidence map›Paper›PMID 36233753›Full record

ArticleJournal of clinical medicine2022

Antidepressant Use and Its Association with 28-Day Mortality in Inpatients with SARS-CoV-2: Support for the FIASMA Model against COVID-19.

Nicolas Hoertel, Marina Sánchez-Rico, Johannes Kornhuber, Erich Gulbins, Angela M Reiersen, Eric J Lenze, Bradley A Fritz, Farid Jalali, Edward J Mills, Céline Cougoule and 10 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Efficacy and safety of selective serotonin reuptake inhibitors in COVID-19 management: a systematic review and meta-analysis.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
    Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Nicolas HoertelInstitut de Psychiatrie et Neuroscience de Paris, Université Paris Cité, INSERM U1266, F-75014 Paris, France.ORCID 0000-0002-7890-1349
Marina Sánchez-RicoAP-HP, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Issy-les-Moulineaux, F-92130 Paris, France.ORCID 0000-0002-1121-8641
Johannes KornhuberDepartment of Psychiatry and Psychotherapy, University Hospital, Friedrich-Alexander-University of Erlangen-Nuremberg (FAU), 91054 Erlangen, Germany.ORCID 0000-0002-8096-3987
Erich GulbinsInstitute for Molecular Biology, University Hospital Essen, University of Duisburg-Essen, 47057 Essen, Germany.
Angela M ReiersenDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Eric J LenzeDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Bradley A FritzDepartment of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA.ORCID 0000-0002-7239-8877
Farid JalaliDepartment of Gastroenterology, Saddleback Medical Group, Laguna Hills, CA 92653, USA.
Edward J MillsHealth Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON L8S 4K1, Canada.
Céline CougouleInstitut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, F-31400 Toulouse, France.ORCID 0000-0002-6795-5448
Alexander CarpinteiroInstitute for Molecular Biology, University Hospital Essen, University of Duisburg-Essen, 47057 Essen, Germany.
Christiane MühleDepartment of Psychiatry and Psychotherapy, University Hospital, Friedrich-Alexander-University of Erlangen-Nuremberg (FAU), 91054 Erlangen, Germany.ORCID 0000-0001-7517-9154
Katrin Anne BeckerInstitute for Molecular Biology, University Hospital Essen, University of Duisburg-Essen, 47057 Essen, Germany.ORCID 0000-0002-6317-7298
David R BoulwareDepartment of Medicine, Division of Infectious Diseases and International Medicine, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-4715-0060
Carlos BlancoNational Institute on Drug Abuse (NIDA), National Institutes of Health, Bethesda, MD 20852, USA.
Jesús M AlvaradoDepartment of Psychobiology and Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Pozuelo de Alarcón, 28223 Pozuelo de Alarcón (Madrid), Spain.ORCID 0000-0003-4780-0147
Nathalie Strub-WourgaftCOVID-19 Response & Pandemic Preparedness, Drugs for Neglected Diseases Initiative (DNDi), 1202 Geneva, Switzerland.
Cédric LemogneInstitut de Psychiatrie et Neuroscience de Paris, Université Paris Cité, INSERM U1266, F-75014 Paris, France.
Frédéric LimosinInstitut de Psychiatrie et Neuroscience de Paris, Université Paris Cité, INSERM U1266, F-75014 Paris, France.
On Behalf Of Ap-Hp/Université Paris Cité/Inserm Covid-Research Collaboration Ap-Hp Covid Cdr Initiative And Entrepôt de Données de Santé Ap-Hp Consortium

Funding

PHARMacist and Community Health Support to Optimize Medications After Trauma Surgery (PHARM-C)P50MH122351 · NIMH · WASHINGTON UNIVERSITY · PI Eric J Lenze · 2021 to 2026
$10.8M
NIMH NIH HHS P50 MH122351
6 · The paper itself

Abstract

To reduce Coronavirus Disease 2019 (COVID-19)-related mortality and morbidity, widely available oral COVID-19 treatments are urgently needed. Certain antidepressants, such as fluvoxamine or fluoxetine, may be beneficial against COVID-19. We included 388,945 adult inpatients who tested positive for SARS-CoV-2 at 36 AP−HP (Assistance Publique−Hôpitaux de Paris) hospitals from 2 May 2020 to 2 November 2021. We compared the prevalence of antidepressant use at admission in a 1:1 ratio matched analytic sample with and without COVID-19 (N = 82,586), and assessed its association with 28-day all-cause mortality in a 1:1 ratio matched analytic sample of COVID-19 inpatients with and without antidepressant use at admission (N = 1482). Antidepressant use was significantly less prevalent in inpatients with COVID-19 than in a matched control group of inpatients without COVID-19 (1.9% versus 4.8%; Odds Ratio (OR) = 0.38; 95%CI = 0.35−0.41, p < 0.001). Antidepressant use was significantly associated with reduced 28-day mortality among COVID-19 inpatients (12.8% versus 21.2%; OR = 0.55; 95%CI = 0.41−0.72, p < 0.001), particularly at daily doses of at least 40 mg fluoxetine equivalents. Antidepressants with high FIASMA (Functional Inhibitors of Acid Sphingomyelinase) activity seem to drive both associations. These treatments may reduce SARS-CoV-2 infections and COVID-19-related mortality in inpatients, and may be appropriate for prophylaxis and/or COVID-19 therapy for outpatients or inpatients.

Indexed as

antidepressantceramideCOVID-19FIASMAfluoxetinefluvoxaminemortalitySARS-CoV-2sigma-1 receptorsphingomyelinase

Identifiers

PMID36233753
PMCPMC9572995

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.