The effect of immunosuppressants on the prognosis of SARS-CoV-2 infection

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  • Daniel Ward
  • Sanne Gørtz
  • Martin Thomson Ernst
  • Nynne Nyboe Andersen
  • Kjær, Susanne Krüger
  • Jesper Hallas
  • Steffen Christensen
  • Christian Fynbo Christiansen
  • Simone Bastrup Israelsen
  • Benfield, Thomas
  • Anton Pottegard
  • Tine Jess

Background Immunosuppression may worsen severe acute respiratory syndrome coronavirus 2 (SARSCoV- 2) infection. We conducted a nationwide cohort study of the effect of exposure to immunosuppressants on the prognosis of SARS-CoV-2 infection in Denmark. Methods We identified all SARS-CoV-2 test-positive patients from February 2020 to October 2020 and linked healthcare data from nationwide registers, including prescriptions for the exposure (immunosuppressant drugs). We estimated relative risks of hospital admission, intensive care unit (ICU) admission and death (each studied independently up to 30 days from testing) with a log-linear binomial regression adjusted for confounders using a propensity score-based matching weights model. Results A composite immunosuppressant exposure was associated with a significantly increased risk of death (adjusted relative risk 1.56 (95% CI 1.10-2.22)). The increased risk of death was mainly driven by exposure to systemic glucocorticoids (adjusted relative risk 2.38 (95% CI 1.72-3.30)), which were also associated with an increased risk of hospital admission (adjusted relative risk 1.34 (95% CI 1.10-1.62)), but not of ICU admission (adjusted relative risk 1.76 (95% CI 0.93-3.35)); these risks were greater for high cumulative doses of glucocorticoids than for moderate doses. Exposure to selective immunosuppressants, tumour necrosis factor inhibitors or interleukin inhibitors was not associated with an increased risk of hospitalisation, ICU admission or death, nor was exposure to calcineurin inhibitors, other immunosuppressants, hydroxychloroquine or chloroquine. Conclusions Exposure to glucocorticoids was associated with increased risks of hospital admission and death. Further investigation is needed to determine the optimal management of coronavirus disease 2019 (COVID-19) in patients with pre-morbid glucocorticoid usage, specifically whether these patients require altered doses of glucocorticoids.

OriginalsprogEngelsk
Artikelnummer2100769
TidsskriftEuropean Respiratory Journal
Vol/bind59
Udgave nummer4
ISSN0903-1936
DOI
StatusUdgivet - 2022

Bibliografisk note

Funding Information:
Support statement: T. Jess received financial support from the Lundbeck Foundation (R349-2020-582). Funding information for this article has been deposited with the Crossref Funder Registry.

Funding Information:
Conflict of interest: D. Ward has nothing to disclose. S. Gørtz has nothing to disclose. M. Thomsen Ernst has nothing to disclose. N.N. Andersen has nothing to disclose. S.K. Kjær has nothing to disclose. J. Hallas has nothing to disclose. S. Christensen has nothing to disclose. C. Fynbo Christiansen has nothing to disclose. S. Bastrup Israelsen has nothing to disclose. T. Benfield reports unrestricted grants to his institution from Novo Nordisk Foundation, Simonsen Foundation, Lundbeck Foundation, Kai Foundation, Erik and Susanna Olesen’s Charitable Fund, GSK, Pfizer, Gilead Sciences, MSD; grants from Boehringer Ingelheim, Roche, Novartis, Kancera AB; advisory board membership at GSK, Pfizer, Gilead Sciences, MSD, Pentabase; consulting fees from GSK, Pfizer; lecture fees from GSK, Pfizer, Gilead Sciences, Boehringer Ingelheim, AbbVie; and donation of trial medication (baricitinib) from Eli Lilly. A. Pottegård reports funds paid to his institution from Alcon, Almirall, Astellas, AstraZeneca, Boehringer Ingelheim, Novo Nordisk, Servier and LEO Pharma, outside the submitted work. T. Jess reports a COVID research grant from the Lundbeck Foundation.

Publisher Copyright:
© 2022 European Respiratory Society. All rights reserved.

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