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Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study

BACKGROUND: Limited data exist regarding the disease course of coronavirus disease 2019 (COVID-19) and its relationship with immunosuppressants among patients with immune-mediated inflammatory diseases (IMIDs). Therefore, this study aims to investigate the association between COVID-19, frequent rheu...

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Autores principales: Attauabi, Mohamed, Seidelin, Jakob Benedict, Felding, Oluf Krautwald, Wewer, Mads Damsgaard, Vinther Arp, Laura Kirstine, Sarikaya, Melek Zahra, Egeberg, Alexander, Vladimirova, Nora, Bendtsen, Flemming, Burisch, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879155/
https://www.ncbi.nlm.nih.gov/pubmed/33592545
http://dx.doi.org/10.1016/j.jaut.2021.102613
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author Attauabi, Mohamed
Seidelin, Jakob Benedict
Felding, Oluf Krautwald
Wewer, Mads Damsgaard
Vinther Arp, Laura Kirstine
Sarikaya, Melek Zahra
Egeberg, Alexander
Vladimirova, Nora
Bendtsen, Flemming
Burisch, Johan
author_facet Attauabi, Mohamed
Seidelin, Jakob Benedict
Felding, Oluf Krautwald
Wewer, Mads Damsgaard
Vinther Arp, Laura Kirstine
Sarikaya, Melek Zahra
Egeberg, Alexander
Vladimirova, Nora
Bendtsen, Flemming
Burisch, Johan
author_sort Attauabi, Mohamed
collection PubMed
description BACKGROUND: Limited data exist regarding the disease course of coronavirus disease 2019 (COVID-19) and its relationship with immunosuppressants among patients with immune-mediated inflammatory diseases (IMIDs). Therefore, this study aims to investigate the association between COVID-19, frequent rheumatological, dermatological, gastrointestinal, and neurological IMIDs and immunosuppressants. METHODS: We conducted a Danish population-based cohort study including all residents living within Capital Region of Denmark and Region Zealand from January 28th, 2020 until September 15th, 2020 with the only eligibility criterion being a test for SARS-CoV-2 via reverse transcription–polymerase chain-reaction. Main outcomes included development of COVID-19, COVID-19-related hospitalization and mortality. RESULTS: COVID-19 was less common among patients with IMIDs than the background population (n = 328/20,513 (1.60%) and n = 10,792/583,788(1.85%), p < 0.01, respectively). However, those with IMIDs had a significantly higher risk of COVID-19-related hospitalization (31.1% and 18.6%, p < 0.01, respectively) and mortality (9.8% and 4.3%, p < 0.01, respectively), which were associated with patients older than 65 years, and presence of comorbidities. Furthermore, systemic steroids were independently associated with a severe course of COVID-19 (Odds ratio (OR) = 3.56 (95%CI 1.83–7.10), p < 0.01), while biologic therapies were associated with a reduced risk hereof (OR = 0.47 (95%CI 0.22–0.95), p = 0.04). Patients suspending immunosuppressants due to COVID-19 had an increased risk of subsequent hospitalization (OR = 3.59 (95%CI 1.31–10.78), p = 0.02). CONCLUSION: This study found a lower occurrence, but a more severe disease course, of COVID-19 among patients with IMIDs, which was associated with the use of systemic steroids for IMIDs and suspension of other immunosuppressants. This study emphasizes the importance of weighing risks before suspending immunosuppressants during COVID-19.
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spelling pubmed-78791552021-02-16 Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study Attauabi, Mohamed Seidelin, Jakob Benedict Felding, Oluf Krautwald Wewer, Mads Damsgaard Vinther Arp, Laura Kirstine Sarikaya, Melek Zahra Egeberg, Alexander Vladimirova, Nora Bendtsen, Flemming Burisch, Johan J Autoimmun Article BACKGROUND: Limited data exist regarding the disease course of coronavirus disease 2019 (COVID-19) and its relationship with immunosuppressants among patients with immune-mediated inflammatory diseases (IMIDs). Therefore, this study aims to investigate the association between COVID-19, frequent rheumatological, dermatological, gastrointestinal, and neurological IMIDs and immunosuppressants. METHODS: We conducted a Danish population-based cohort study including all residents living within Capital Region of Denmark and Region Zealand from January 28th, 2020 until September 15th, 2020 with the only eligibility criterion being a test for SARS-CoV-2 via reverse transcription–polymerase chain-reaction. Main outcomes included development of COVID-19, COVID-19-related hospitalization and mortality. RESULTS: COVID-19 was less common among patients with IMIDs than the background population (n = 328/20,513 (1.60%) and n = 10,792/583,788(1.85%), p < 0.01, respectively). However, those with IMIDs had a significantly higher risk of COVID-19-related hospitalization (31.1% and 18.6%, p < 0.01, respectively) and mortality (9.8% and 4.3%, p < 0.01, respectively), which were associated with patients older than 65 years, and presence of comorbidities. Furthermore, systemic steroids were independently associated with a severe course of COVID-19 (Odds ratio (OR) = 3.56 (95%CI 1.83–7.10), p < 0.01), while biologic therapies were associated with a reduced risk hereof (OR = 0.47 (95%CI 0.22–0.95), p = 0.04). Patients suspending immunosuppressants due to COVID-19 had an increased risk of subsequent hospitalization (OR = 3.59 (95%CI 1.31–10.78), p = 0.02). CONCLUSION: This study found a lower occurrence, but a more severe disease course, of COVID-19 among patients with IMIDs, which was associated with the use of systemic steroids for IMIDs and suspension of other immunosuppressants. This study emphasizes the importance of weighing risks before suspending immunosuppressants during COVID-19. Elsevier Ltd. 2021-03 2021-02-12 /pmc/articles/PMC7879155/ /pubmed/33592545 http://dx.doi.org/10.1016/j.jaut.2021.102613 Text en © 2021 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Attauabi, Mohamed
Seidelin, Jakob Benedict
Felding, Oluf Krautwald
Wewer, Mads Damsgaard
Vinther Arp, Laura Kirstine
Sarikaya, Melek Zahra
Egeberg, Alexander
Vladimirova, Nora
Bendtsen, Flemming
Burisch, Johan
Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title_full Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title_fullStr Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title_full_unstemmed Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title_short Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study
title_sort coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – a danish population-based cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879155/
https://www.ncbi.nlm.nih.gov/pubmed/33592545
http://dx.doi.org/10.1016/j.jaut.2021.102613
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