The "sex gap" in COVID-19 trials: a scoping review.

COVID-19 Clinical trials Diversity Sex Therapy

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 05 08 2020
revised: 22 10 2020
accepted: 30 10 2020
pubmed: 8 12 2020
medline: 8 12 2020
entrez: 7 12 2020
Statut: ppublish

Résumé

Many studies investigate the role of pharmacological treatments on disease course in Corona Virus Disease 2019 (COVID-19). Sex disparities in genetics, immunological responses, and hormonal mechanisms may underlie the substantially higher fatality rates reported in male COVID-19 patients. To optimise care for COVID-19 patients, prophylactic and therapeutic studies should include sex-specific design and analyses. Therefore, in this scoping review, we investigated whether studies on pharmacological treatment in COVID-19 were performed based on a priori sex-specific design or post-hoc sex-specific analyses. We systematically searched PubMed, EMBASE, UpToDate, clinical trial.org, and MedRxiv for studies on pharmacological treatment for COVID-19 until June 6th, 2020. We included case series, randomized controlled trials, and observational studies in humans (≥18 years) investigating antiviral, antimalarial, and immune system modulating drugs. Data were collected on 1) the proportion of included females, 2) whether sex stratification was performed (a priori by design or post-hoc), and 3) whether effect modification by sex was investigated. 30 studies were eligible for inclusion, investigating remdesivir ( Analyses assessing potential interference of sex with (side-)effects of pharmacological therapy for COVID-19 are rarely reported. Considering sex differences in case-fatality rates and genetic, immunological, and hormonal mechanisms, studies should include sex-specific analyses in their design to optimise COVID-19 care. None.

Sections du résumé

BACKGROUND BACKGROUND
Many studies investigate the role of pharmacological treatments on disease course in Corona Virus Disease 2019 (COVID-19). Sex disparities in genetics, immunological responses, and hormonal mechanisms may underlie the substantially higher fatality rates reported in male COVID-19 patients. To optimise care for COVID-19 patients, prophylactic and therapeutic studies should include sex-specific design and analyses. Therefore, in this scoping review, we investigated whether studies on pharmacological treatment in COVID-19 were performed based on a priori sex-specific design or post-hoc sex-specific analyses.
METHODS METHODS
We systematically searched PubMed, EMBASE, UpToDate, clinical trial.org, and MedRxiv for studies on pharmacological treatment for COVID-19 until June 6th, 2020. We included case series, randomized controlled trials, and observational studies in humans (≥18 years) investigating antiviral, antimalarial, and immune system modulating drugs. Data were collected on 1) the proportion of included females, 2) whether sex stratification was performed (a priori by design or post-hoc), and 3) whether effect modification by sex was investigated.
FINDINGS RESULTS
30 studies were eligible for inclusion, investigating remdesivir (
INTERPRETATION CONCLUSIONS
Analyses assessing potential interference of sex with (side-)effects of pharmacological therapy for COVID-19 are rarely reported. Considering sex differences in case-fatality rates and genetic, immunological, and hormonal mechanisms, studies should include sex-specific analyses in their design to optimise COVID-19 care.
FUNDING BACKGROUND
None.

Identifiants

pubmed: 33283178
doi: 10.1016/j.eclinm.2020.100652
pii: S2589-5370(20)30396-5
pmc: PMC7701906
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100652

Informations de copyright

© 2020 The Authors.

Déclaration de conflit d'intérêts

Dr. Marx reports grants and personal fees from Bbraun Melsungen AG, grants and personal fees from Sphingotec AG, grants and personal fees from 4TEEN4 Pharmaceuticals GmbH, outside the submitted work. In addition, Dr. Marx has a patent Modulation ofTLR4 signalling European Patent 2855519/US Patent: US9,745,369 B2 issued, and a patent Combination of C1-Inh and Lung surfactant for the treatment of respiratory disorders PatentÐo.: US 7053,176 B1 PCT/EP99/06845 issued. All other authors declare no interest. Furthermore, there are no known conflicts of interest associated with this publication, and there has been no significant financial support for this work that could have influenced its outcome. We confirm that the manuscript has been read and approved by all named authors and that there are no other persons who satisfied the criteria for authorship but are not listed. We further confirm that all have approved the order of authors listed in the manuscript.

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Auteurs

Veronique M M M Schiffer (VMMM)

Department of Obstetrics and Gynaecology, Maastricht University Medical Centre (MUMC+), Maastricht, the Netherlands.
GROW, School for Oncology and Developmental Biology, Maastricht University, the Netherlands.

Emma B N J Janssen (EBNJ)

Department of Obstetrics and Gynaecology, Maastricht University Medical Centre (MUMC+), Maastricht, the Netherlands.
Cardiovascular Research Institute Maastricht (CARIM), Maastricht, the Netherlands.

Bas C T van Bussel (BCT)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.
Care and Public Health Research Institute (CAPHRI), Maastricht University, the Netherlands.

Laura L M Jorissen (LLM)

Department of Obstetrics and Gynaecology, Maastricht University Medical Centre (MUMC+), Maastricht, the Netherlands.

Jeanette Tas (J)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.

Jan-Willem E M Sels (JEM)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.
Department of Cardiology, MUMC+, Maastricht, MD 6200, the Netherlands.

Dennis C J J Bergmans (DCJJ)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.

Trang H T Dinh (THT)

Department of Cardiology, MUMC+, Maastricht, MD 6200, the Netherlands.

Sander M J van Kuijk (SMJ)

Department of Clinical Epidemiology and Medical Technology Assessment, MUMC+, Maastricht, the Netherlands.

Anisa Hana (A)

Department of Intensive Care, Laurentius Ziekenhuis, Roermond, the Netherlands.

Jannet Mehagnoul-Schipper (J)

Department of Intensive Care, VieCuri Medisch Centrum, Venlo, the Netherlands.

Clarissa I E Scheeren (CIE)

Department of Intensive Care, Zuyderland Medisch Centrum, the Netherlands.

Dieter Mesotten (D)

Department of Intensive Care, Ziekenhuis Oost-Limburg, Genk, Belgium.

Bjorn Stessel (B)

Department of Intensive Care, Jessa Hospital, Hasselt, Belgium.

Gernot Marx (G)

Department of Intensive Care, Uniklinik RWTH Aachen, Aachen, Germany.

Arnoud W J van T Hof (AWJVT)

Department of Cardiology, MUMC+, Maastricht, MD 6200, the Netherlands.

Marc E A Spaanderman (MEA)

Department of Obstetrics and Gynaecology, Maastricht University Medical Centre (MUMC+), Maastricht, the Netherlands.
Department of Obstetrics and Gynaecology, Radboud University Medical Centre, Nijmegen, the Netherlands.

Walther N K A van Mook (WNKA)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.
School of Health Professions Education, Academy for Postgraduate Medical Training, Maastricht University, Maastricht, the Netherlands.

Iwan C C van der Horst (ICC)

Department of Intensive Care, MUMC+, Maastricht, the Netherlands.
Cardiovascular Research Institute Maastricht (CARIM), Maastricht, the Netherlands.

Chahinda Ghossein-Doha (C)

Department of Obstetrics and Gynaecology, Maastricht University Medical Centre (MUMC+), Maastricht, the Netherlands.
Department of Intensive Care, MUMC+, Maastricht, the Netherlands.
Department of Cardiology, MUMC+, Maastricht, MD 6200, the Netherlands.
Cardiovascular Research Institute Maastricht (CARIM), Maastricht, the Netherlands.

Classifications MeSH