Association Between FIASMAs and Reduced Risk of Intubation or Death in Individuals Hospitalized for Severe COVID-19: An Observational Multicenter Study.


Journal

Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741

Informations de publication

Date de publication:
12 2021
Historique:
received: 02 03 2021
accepted: 20 05 2021
pubmed: 30 5 2021
medline: 24 11 2021
entrez: 29 5 2021
Statut: ppublish

Résumé

Several medications commonly used for a number of medical conditions share a property of functional inhibition of acid sphingomyelinase (ASM), or FIASMA. Preclinical and clinical evidence suggest that the ASM/ceramide system may be central to severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) infection. We examined the potential usefulness of FIASMA use among patients hospitalized for severe coronavirus disease 2019 (COVID-19) in an observational multicenter study conducted at Greater Paris University hospitals. Of 2,846 adult patients hospitalized for severe COVID-19, 277 (9.7%) were taking an FIASMA medication at the time of their hospital admission. The primary end point was a composite of intubation and/or death. We compared this end point between patients taking vs. not taking an FIASMA medication in time-to-event analyses adjusted for sociodemographic characteristics and medical comorbidities. The primary analysis was a Cox regression model with inverse probability weighting (IPW). Over a mean follow-up of 9.2 days (SD = 12.5), the primary end point occurred in 104 patients (37.5%) receiving an FIASMA medication, and 1,060 patients (41.4%) who did not. Despite being significantly and substantially associated with older age and greater medical severity, FIASMA medication use was significantly associated with reduced likelihood of intubation or death in both crude (hazard ratio (HR) = 0.71, 95% confidence interval (CI) = 0.58-0.87, P < 0.001) and primary IPW (HR = 0.58, 95%CI = 0.46-0.72, P < 0.001) analyses. This association remained significant in multiple sensitivity analyses and was not specific to one particular FIASMA class or medication. These results show the potential importance of the ASM/ceramide system in COVID-19 and support the continuation of FIASMA medications in these patients. Double-blind controlled randomized clinical trials of these medications for COVID-19 are needed.

Identifiants

pubmed: 34050932
doi: 10.1002/cpt.2317
pmc: PMC8239599
doi:

Substances chimiques

Enzyme Inhibitors 0
SMPD1 protein, human EC 3.1.4.12
Sphingomyelin Phosphodiesterase EC 3.1.4.12

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1498-1511

Investigateurs

Pierre-Yves Ancel (PY)
Alain Bauchet (A)
Nathanaël Beeker (N)
Vincent Benoit (V)
Mélodie Bernaux (M)
Ali Bellamine (A)
Romain Bey (R)
Aurélie Bourmaud (A)
Stéphane Breant (S)
Anita Burgun (A)
Fabrice Carrat (F)
Charlotte Caucheteux (C)
Julien Champ (J)
Sylvie Cormont (S)
Christel Daniel (C)
Julien Dubiel (J)
Catherine Ducloas (C)
Loic Esteve (L)
Marie Frank (M)
Nicolas Garcelon (N)
Alexandre Gramfort (A)
Nicolas Griffon (N)
Olivier Grisel (O)
Martin Guilbaud (M)
Claire Hassen-Khodja (C)
François Hemery (F)
Martin Hilka (M)
Anne Sophie Jannot (A)
Jerome Lambert (J)
Richard Layese (R)
Judith Leblanc (J)
Léo Lebouter (L)
Guillaume Lemaitre (G)
Damien Leprovost (D)
Ivan Lerner (I)
Kankoe Levi Sallah (K)
Aurélien Maire (A)
Marie-France Mamzer (MF)
Patricia Martel (P)
Arthur Mensch (A)
Thomas Moreau (T)
Antoine Neuraz (A)
Nina Orlova (N)
Nicolas Paris (N)
Bastien Rance (B)
Hélène Ravera (H)
Antoine Rozes (A)
Elisa Salamanca (E)
Arnaud Sandrin (A)
Patricia Serre (P)
Xavier Tannier (X)
Jean-Marc Treluyer (JM)
Damien van Gysel (D)
Gaël Varoquaux (G)
Jill Jen Vie (JJ)
Maxime Wack (M)
Perceval Wajsburt (P)
Demian Wassermann (D)
Eric Zapletal (E)

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Nicolas Hoertel (N)

Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.

Marina Sánchez-Rico (M)

Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.
Department of Psychobiology and Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Pozuelo de Alarcón, Madrid, Spain.

Erich Gulbins (E)

Institute for Molecular Biology, University Medicine Essen, University of Duisburg-Essen, Essen, Germany.

Johannes Kornhuber (J)

Department of Psychiatry and Psychotherapy, University Hospital, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.

Alexander Carpinteiro (A)

Institute for Molecular Biology, University Medicine Essen, University of Duisburg-Essen, Essen, Germany.
Department of Hematology and Stem Cell Transplantation, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Eric J Lenze (EJ)

Department of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.

Angela M Reiersen (AM)

Department of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.

Miriam Abellán (M)

Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.

Pedro de la Muela (P)

Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.
Department of Psychobiology and Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Pozuelo de Alarcón, Madrid, Spain.

Raphaël Vernet (R)

Medical Informatics, Biostatistics and Public Health Department, Assistance Publique-Hopitaux de Paris, Centre-Université de Paris, Hôpital Européen Georges Pompidou, Paris, France.

Carlos Blanco (C)

Division of Epidemiology, Services, and Prevention Research, National Institute on Drug Abuse, North Bethesda, Maryland, USA.

Céline Cougoule (C)

Institut de Pharmacologie et de Biologie Structurale, IPBS, Université de Toulouse, Toulouse, France.

Nathanaël Beeker (N)

Unité de Recherche clinique, Hopital Cochin, Assistance Publique-Hopitaux de Paris, Paris, France.

Antoine Neuraz (A)

INSERM, UMR_S 1138, Cordeliers Research Center, Université de Paris, Paris, France.
Department of Medical Informatics, Necker-Enfants Malades Hospital, Assistance Publique-Hopitaux de Paris, Centre-Université de Paris, Paris, France.

Philip Gorwood (P)

INSERM, U1266 (Institute of Psychiatry and Neuroscience of Paris), Université de Paris, Paris, France.

Jesús M Alvarado (JM)

Department of Psychobiology and Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Pozuelo de Alarcón, Madrid, Spain.

Pierre Meneton (P)

INSERM U1142 LIMICS, UMRS 1142, Sorbonne Universities, UPMC University of Paris 06, University of Paris 13, Paris, France.

Frédéric Limosin (F)

Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.

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