Association Between FIASMAs and Reduced Risk of Intubation or Death in Individuals Hospitalized for Severe COVID-19: An Observational Multicenter Study.
Adolescent
Adult
Aged
Aged, 80 and over
COVID-19
/ enzymology
COVID-19 Testing
/ trends
Cohort Studies
Enzyme Inhibitors
/ pharmacology
Female
Hospitalization
/ trends
Humans
Intubation, Intratracheal
/ mortality
Male
Middle Aged
Mortality
/ trends
Retrospective Studies
Sphingomyelin Phosphodiesterase
/ antagonists & inhibitors
Young Adult
COVID-19 Drug Treatment
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
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
1498-1511Investigateurs
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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