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COVID-19 outcomes in patients with multiple sclerosis: Understanding changes from 2020 to 2022.
Jeantin, Lina; Januel, Edouard; Labauge, Pierre; Maillart, Elisabeth; de Seze, Jérôme; Zéphir, Hélène; Pelletier, Jean; Kerschen, Philippe; Biotti, Damien; Heinzlef, Olivier; Guilloton, Laurent; Bensa, Caroline; Théaudin, Marie; Vukusic, Sandra; Casez, Olivier; Maurousset, Aude; Laplaud, David; Berger, Eric; Lebrun-Frenay, Christine; Bourre, Bertrand; Branger, Pierre; Stankoff, Bruno; Clavelou, Pierre; Thouvenot, Eric; Manchon, Eric; Moreau, Thibault; Sellal, François; Zedet, Mickaël; Papeix, Caroline; Louapre, Céline.
Afiliação
  • Jeantin L; Sorbonne University, Paris Brain Institute-ICM, Assistance Publique-Hôpitaux de Paris (AP-HP), Inserm, CNRS, Hôpital de la Pitié Salpêtrière, CIC Neurosciences, FCRIN4MS, Paris, France.
  • Januel E; Sorbonne University, Paris Brain Institute-ICM, Assistance Publique-Hôpitaux de Paris (AP-HP), Inserm, CNRS, Hôpital de la Pitié Salpêtrière, CIC Neurosciences, FCRIN4MS, Paris, France/Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Assistance Publique-Hôpita
  • Labauge P; Department of Neurology, CRC-SEP, Montpellier University Hospital, Montpellier, France/ Institute for Neurosciences of Montpellier (INM), INSERM and University of Montpellier, Montpellier, France.
  • Maillart E; Sorbonne University, Paris Brain Institute-ICM, Assistance Publique-Hôpitaux de Paris (AP-HP), Inserm, CNRS, Hôpital de la Pitié Salpêtrière, CIC Neurosciences, FCRIN4MS, Paris, France.
  • de Seze J; Department of Neurology and Clinical Investigation Center, CIC 1434, INSERM 1434, CHU de Strasbourg, Strasbourg, France.
  • Zéphir H; Department of Neurology, CHU Lille, INSERM U1172, University of Lille, Lille, France.
  • Pelletier J; Aix-Marseille Universite, APHM, Hôpital de la Timone, Pôle de Neurosciences Cliniques, Service de Neurologie, Marseille, France.
  • Kerschen P; Department of Neurology, Luxembourg Hospital Center, Luxembourg City, Luxembourg.
  • Biotti D; Centre Ressources et Compétences sclérose en plaques (CRC-SEP) et Service de Neurologie B4, Hôpital Pierre-Paul Riquet, CHU Toulouse Purpan, Toulouse, France/ INSERM UMR1291-CNRS UMR5051, Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), Université Toulouse 3, Toulouse, Fra
  • Heinzlef O; Département de Neurologie, CRC SEP, Centre Hospitalier intercommunal de Poissy-Saint-Germain-en-Laye, Poissy, France.
  • Guilloton L; Association des Neurologues Libéraux de Langue Française, Rambouillet, France.
  • Bensa C; Département de Neurologie, Hôpital Fondation Adolphe de Rothschild, Paris, France.
  • Théaudin M; Department of Clinical Neurosciences, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
  • Vukusic S; Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Service de Neurologie, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Inflammation, Bron, France.
  • Casez O; Neurologie, Pathologies Inflammatoires du Système Nerveux, CHU Grenoble Alpes, Grenoble, France/ TIMC-IMAG, Translational Research in Autoimmunity and Inflammation Group (T-RAIG), Université Grenoble Alpes, Grenoble, France.
  • Maurousset A; CRC SEP and Department of Neurology, CHU de Tours, Hôpital Bretonneau, Tours, France.
  • Laplaud D; CR2TI UMR1064, Service de Neurologie and CIC0004 INSERM, CHU de Nantes, Nantes, France.
  • Berger E; Service de Neurologie, CHU de Besançon, Besançon, France.
  • Lebrun-Frenay C; CRCSEP Cote d'Azur, CHU de Nice Pasteur2, Université Nice Cote d'Azur, UR2CA-URRIS, Nice, France.
  • Bourre B; Department of Neurology, CHU Rouen, Rouen, France.
  • Branger P; Service de Neurologie, CHU de Caen Normandie, Caen, France.
  • Stankoff B; Assistance Publique-Hôpitaux de Paris (AP-HP), Sorbonne Université, Department of Neurology, Saint Antoine Hospital, CRCSEP, Paris, France.
  • Clavelou P; CRCSEP, Department of Neurology, CHU Clermont-Ferrand, Inserm, Neuro-Dol, Clermont-Ferrand, France.
  • Thouvenot E; Department of Neurology, Nimes University Hospital, Nimes Cedex 9 F-30029, France; Institut de Génomique Fonctionnelle, UMR5203, INSERM 1191, Université de Montpellier, Montpellier, France.
  • Manchon E; Department of Neurology, Gonesse Hospital, Gonesse, France.
  • Moreau T; EA4184, Department of Neurology, CHU de Dijon, Dijon, France.
  • Sellal F; Département de Neurologie, Hôpitaux Civils de Colmar, Colmar, France; Unité INSERM U-1118, Faculté de Médecine, Université de Strasbourg, Strasbourg, France.
  • Zedet M; Department of Neurology, AP-HP, Henri Mondor University Hospital, Université Paris Est Créteil, Creteil, France.
  • Papeix C; Département de Neurologie, Hôpital Fondation Adolphe de Rothschild, Paris, France.
  • Louapre C; Sorbonne University, Paris Brain Institute-ICM, Assistance Publique-Hôpitaux de Paris (AP-HP), Inserm, CNRS, Hôpital de la Pitié Salpêtrière, CIC Neurosciences, FCRIN4MS, Paris, France.
Mult Scler ; 30(3): 381-395, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38247113
ABSTRACT

BACKGROUND:

Epidemiologic studies on coronavirus disease 2019 (COVID-19) in patients with multiple sclerosis (pwMS) have focused on the first waves of the pandemic until early 2021.

OBJECTIVES:

We aimed to extend these data from the onset of the pandemic to the global coverage by vaccination in summer 2022.

METHODS:

This retrospective, multicenter observational study analyzed COVISEP registry data on reported COVID-19 cases in pwMS between January 2020 and July 2022. Severe COVID-19 was defined as hospitalization or higher severity.

RESULTS:

Among 2584 pwMS with confirmed/highly suspected COVID-19, severe infection rates declined from 14.6% preomicron wave to 5.7% during omicron wave (p < 0.001). Multivariate analysis identified age (odds ratio (OR) = 1.43, 95% confidence interval (CI) = [1.25-1.64] per 10 years), male sex (OR = 2.01, 95% CI = [1.51-2.67]), obesity (OR = 2.36, 95% CI = [1.52-3.68]), cardiac comorbidities (OR = 2.36, 95% CI = [1.46-3.83]), higher Expanded Disability Status Scale (EDSS) scores (OR = 2.09, 95% CI = [1.43-3.06] for EDSS 3-5.5 and OR = 4.53, 95% CI = [3.04-6.75] for EDSS ⩾6), and anti-CD20 therapies (OR = 2.67, 95% CI = [1.85-3.87]) as risk factors for COVID-19 severity. Vaccinated individuals experienced less severe COVID-19, whether on (risk ratio (RR) = 0.64, 95% CI = [0.60-0.69]) or off (RR = 0.32, 95% CI = [0.30-0.33]) anti-CD20.

DISCUSSION:

In pwMS, consistent risk factors were anti-CD20 therapies and neurological disability, emerging as vital drivers of COVID-19 severity regardless of wave, period, or vaccination status.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 / Esclerose Múltipla Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 / Esclerose Múltipla Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article