CovAID: Identification of factors associated with severe COVID-19 in patients with inflammatory rheumatism or autoimmune diseases.

COVID-19 auto-immune diseases inflammatory rheumatic diseases lupus rheumatic and musculoskeletal diseases rituximab vasculitis

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2023
Historique:
received: 27 01 2023
accepted: 27 02 2023
medline: 11 4 2023
entrez: 10 4 2023
pubmed: 11 4 2023
Statut: epublish

Résumé

Autoimmune/inflammatory rheumatic diseases (AIRDs) patients might be at-risk of severe COVID-19. However, whether this is linked to the disease or to its treatment is difficult to determine. This study aimed to identify factors associated with occurrence of severe COVID-19 in AIRD patients and to evaluate whether having an AIRD was associated with increased risk of severe COVID-19 or death. Two databases were analyzed: the EDS (Entrepôt des Données de Santé, Clinical Data Warehouse), including all patients followed in Paris university hospitals and the French multi-center COVID-19 cohort [French rheumatic and musculoskeletal diseases (RMD)]. First, in a combined analysis we compared patients with severe and non-severe COVID-19 to identify factors associated with severity. Then, we performed a propensity matched score case-control study within the EDS database to compare AIRD cases and non-AIRD controls. Among 1,213 patients, 195 (16.1%) experienced severe COVID-19. In multivariate analysis, older age, interstitial lung disease (ILD), arterial hypertension, obesity, sarcoidosis, vasculitis, auto-inflammatory diseases, and treatment with corticosteroids or rituximab were associated with increased risk of severe COVID-19. Among 35,741 COVID-19 patients in EDS, 316 having AIRDs were compared to 1,264 Propensity score-matched controls. AIRD patients had a higher risk of severe COVID-19 [aOR = 1.43 (1.08-1.87), p = 0.01] but analysis restricted to rheumatoid arthritis and spondyloarthritis found no increased risk of severe COVID-19 [aOR = 1.11 (0.68-1.81)]. In this multicenter study, we confirmed that AIRD patients treated with rituximab or corticosteroids and/or having vasculitis, auto-inflammatory disease, and sarcoidosis had increased risk of severe COVID-19. Also, AIRD patients had, overall, an increased risk of severe COVID-19 compares general population.

Identifiants

pubmed: 37035330
doi: 10.3389/fmed.2023.1152587
pmc: PMC10075312
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1152587

Informations de copyright

Copyright © 2023 Chevalier, Genin, Jean, Avouac, Flipo, Georgin-Lavialle, El Mahou, Pertuiset, Pham, Servettaz, Marotte, Domont, Chazerain, Devaux, Mekinian, Sellam, Fautrel, Rouzaud, Ebstein, Costedoat-Chalumeau, Richez, Hachulla, Mariette and Seror.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Kevin Chevalier (K)

Department of Rheumatology, Université Paris-Saclay, INSERM UMR 1184: Center for Immunology of Viral Infections and Autoimmune Diseases, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.

Michaël Genin (M)

University of Lille, CHU Lille, ULR 2694-METRICS: Evaluation des Technologies de Santé et des Pratiques Médicales, Lille, France.

Thomas Petit Jean (TP)

AP-HP, Département Innovation et Données, Paris, France.

Jerôme Avouac (J)

Cochin Hospital, Rheumatology A, Paris, France.

Rene-Marc Flipo (RM)

Université de Lille, Rheumatology, Lille, France.

Sophie Georgin-Lavialle (S)

Tenon Hospital, Internal Medicine, Paris, France.

Soumaya El Mahou (S)

Hospital Center De Tourcoing, Rheumatology, Tourcoing, France.

Edouard Pertuiset (E)

Hospital Rene Dubos, Rheumatology, Pontoise, France.

Thao Pham (T)

Hospital Sainte Marguerite, Rheumatology, Marseille, France.

Amelie Servettaz (A)

Hospital Robert Debré, Internal Medicine, Infectious Diseases and Clinical Immunology, Reims, France.

Hubert Marotte (H)

University Hospital of Saint-Étienne, Rheumatology, Saint-Priest-en-Jarez, France.

Fanny Domont (F)

University Hospitals Pitié Salpêtrière - Charles Foix, Internal Medicine and Clinical Immunology, Paris, France.

Pascal Chazerain (P)

Hopital de la Croix Saint-Simon, Rheumatology and Internal Medicine, Paris, France.

Mathilde Devaux (M)

Saint-Germain-en-Laye Intercommunal Hospital Center, Internal Medicine, Poissy, France.

Arsene Mekinian (A)

Hospital Saint-Antoine AP-HP, Internal Medicine, Paris, France.

Jérémie Sellam (J)

Hospital Saint-Antoine AP-HP, Rheumatology, Paris, France.

Bruno Fautrel (B)

Sorbonne Universite - APHP, Pitie Salpetriere Hospital, Department of Rheumatology, Pierre Louis Institute of Epidemiology and Public Health, INSERM UMRS 1136, Paris, France.

Diane Rouzaud (D)

Bichat-Claude Bernard Hospital, Internal Medicine, Paris, France.

Esther Ebstein (E)

Bichat-Claude Bernard Hospital, Rheumatology, Paris, France.

Nathalie Costedoat-Chalumeau (N)

Cochin Hospital, Internal Medicine, Paris, France.

Christophe Richez (C)

Chu Bordeaux - Site Pellegrin, Rheumatology, Bordeaux, France.

Eric Hachulla (E)

Department of Internal Medicine and Clinical Immunology, Referral Centre for Centre for Rare Systemic Autoimmune Diseases North and North-West of France (CeRAINO), CHU Lille, University of Lille, INSERM, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, France.

Xavier Mariette (X)

Department of Rheumatology, Université Paris-Saclay, INSERM UMR 1184: Center for Immunology of Viral Infections and Autoimmune Diseases, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.

Raphaèle Seror (R)

Department of Rheumatology, Université Paris-Saclay, INSERM UMR 1184: Center for Immunology of Viral Infections and Autoimmune Diseases, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.

Classifications MeSH