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

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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.

I: Journal of Autoimmunity, Bind 118, 102613, 03.2021.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Attauabi, M, Seidelin, JB, Felding, OK, Wewer, MD, Vinther Arp, LK, Sarikaya, MZ, Egeberg, A, Vladimirova, N, Bendtsen, F & Burisch, J 2021, 'Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study', Journal of Autoimmunity, bind 118, 102613. https://doi.org/10.1016/j.jaut.2021.102613

APA

Attauabi, M., Seidelin, J. B., Felding, O. K., Wewer, M. D., Vinther Arp, L. K., Sarikaya, M. Z., Egeberg, A., Vladimirova, N., Bendtsen, F., & Burisch, J. (2021). Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study. Journal of Autoimmunity, 118, [102613]. https://doi.org/10.1016/j.jaut.2021.102613

Vancouver

Attauabi M, Seidelin JB, Felding OK, Wewer MD, Vinther Arp LK, Sarikaya MZ o.a. Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study. Journal of Autoimmunity. 2021 mar.;118. 102613. https://doi.org/10.1016/j.jaut.2021.102613

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. / Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study. I: Journal of Autoimmunity. 2021 ; Bind 118.

Bibtex

@article{cd167a25424149cfbc0916d9fe0f2776,
title = "Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study",
abstract = "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.",
keywords = "Autoimmune diseases, COVID-19, Epidemiology, Immune-mediated inflammatory diseases, Immunosuppressive agents, Population-based",
author = "Mohamed Attauabi and Seidelin, {Jakob Benedict} and Felding, {Oluf Krautwald} and Wewer, {Mads Damsgaard} and {Vinther Arp}, {Laura Kirstine} and Sarikaya, {Melek Zahra} and Alexander Egeberg and Nora Vladimirova and Flemming Bendtsen and Johan Burisch",
year = "2021",
month = mar,
doi = "10.1016/j.jaut.2021.102613",
language = "English",
volume = "118",
journal = "Journal of Autoimmunity",
issn = "0896-8411",
publisher = "Academic Press",

}

RIS

TY - JOUR

T1 - Coronavirus disease 2019, immune-mediated inflammatory diseases and immunosuppressive therapies – A Danish population-based cohort study

AU - Attauabi, Mohamed

AU - Seidelin, Jakob Benedict

AU - Felding, Oluf Krautwald

AU - Wewer, Mads Damsgaard

AU - Vinther Arp, Laura Kirstine

AU - Sarikaya, Melek Zahra

AU - Egeberg, Alexander

AU - Vladimirova, Nora

AU - Bendtsen, Flemming

AU - Burisch, Johan

PY - 2021/3

Y1 - 2021/3

N2 - 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.

AB - 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.

KW - Autoimmune diseases

KW - COVID-19

KW - Epidemiology

KW - Immune-mediated inflammatory diseases

KW - Immunosuppressive agents

KW - Population-based

U2 - 10.1016/j.jaut.2021.102613

DO - 10.1016/j.jaut.2021.102613

M3 - Journal article

C2 - 33592545

AN - SCOPUS:85100850314

VL - 118

JO - Journal of Autoimmunity

JF - Journal of Autoimmunity

SN - 0896-8411

M1 - 102613

ER -

ID: 260305960