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Confirmed disability progression as a marker of permanent disability in multiple sclerosis.
Sharmin, Sifat; Bovis, Francesca; Malpas, Charles; Horakova, Dana; Havrdova, Eva Kubala; Izquierdo, Guillermo; Eichau, Sara; Trojano, Maria; Prat, Alexandre; Girard, Marc; Duquette, Pierre; Onofrj, Marco; Lugaresi, Alessandra; Grand'Maison, Francois; Grammond, Pierre; Sola, Patrizia; Ferraro, Diana; Terzi, Murat; Gerlach, Oliver; Alroughani, Raed; Boz, Cavit; Shaygannejad, Vahid; van Pesch, Vincent; Cartechini, Elisabetta; Kappos, Ludwig; Lechner-Scott, Jeannette; Bergamaschi, Roberto; Turkoglu, Recai; Solaro, Claudio; Iuliano, Gerardo; Granella, Franco; Van Wijmeersch, Bart; Spitaleri, Daniele; Slee, Mark; McCombe, Pamela; Prevost, Julie; Ampapa, Radek; Ozakbas, Serkan; Sanchez-Menoyo, Jose Luis; Soysal, Aysun; Vucic, Steve; Petersen, Thor; de Gans, Koen; Butler, Ernest; Hodgkinson, Suzanne; Sidhom, Youssef; Gouider, Riadh; Cristiano, Edgardo; Castillo-Triviño, Tamara; Saladino, Maria Laura.
Afiliación
  • Sharmin S; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Bovis F; Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
  • Malpas C; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Horakova D; Melbourne MS Centre, Department of Neurology, Royal Melbourne Hospital, Melbourne, Australia.
  • Havrdova EK; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.
  • Izquierdo G; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.
  • Eichau S; Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Trojano M; Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Prat A; Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari, Bari, Italy.
  • Girard M; Hopital Notre Dame, Montreal, QC, Canada.
  • Duquette P; CHUM and Universite de Montreal, Montreal, QC, Canada.
  • Onofrj M; Hopital Notre Dame, Montreal, QC, Canada.
  • Lugaresi A; CHUM and Universite de Montreal, Montreal, QC, Canada.
  • Grand'Maison F; Hopital Notre Dame, Montreal, QC, Canada.
  • Grammond P; CHUM and Universite de Montreal, Montreal, QC, Canada.
  • Sola P; Department of Neuroscience, Imaging, and Clinical Sciences, University G. d'Annunzio, Chieti, Italy.
  • Ferraro D; IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italia.
  • Terzi M; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italia.
  • Gerlach O; Neuro Rive-Sud, Greenfield Park, QC, Canada.
  • Alroughani R; CISSS Chaudière-Appalache, Levis, QC, Canada.
  • Boz C; Department of Neuroscience, Azienda Ospedaliera Universitaria, Modena, Italy.
  • Shaygannejad V; Department of Neuroscience, Azienda Ospedaliera Universitaria, Modena, Italy.
  • van Pesch V; Medical Faculty, 19 Mayis University, Samsun, Turkey.
  • Cartechini E; Department of Neurology, Zuyderland Medical Center, Sittard-Geleen, The Netherlands.
  • Kappos L; Division of Neurology, Department of Medicine, Amiri Hospital, Sharq, Kuwait.
  • Lechner-Scott J; KTU Medical Faculty Farabi Hospital, Trabzon, Turkey.
  • Bergamaschi R; Isfahan University of Medical Sciences, Isfahan, Iran.
  • Turkoglu R; Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Solaro C; Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Iuliano G; UOC Neurologia, Azienda Sanitaria Unica Regionale Marche - AV3, Macerata, Italy.
  • Granella F; Neurologic Clinic and Policlinic, Departments of Medicine and Clinical Research, University Hospital and University of Basel, Basel, Switzerland.
  • Van Wijmeersch B; School of Medicine and Public Health, University Newcastle, Newcastle, NSW, Australia.
  • Spitaleri D; Department of Neurology, John Hunter Hospital, Hunter New England Health, Newcastle, NSW, Australia.
  • Slee M; IRCCS Mondino Foundation, Pavia, Italy.
  • McCombe P; Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.
  • Prevost J; Department of Rehabilitaiton, ML Novarese Hospital, Moncrivello, Italy.
  • Ampapa R; Ospedali Riuniti di Salerno, Salerno, Italy.
  • Ozakbas S; Department of Medicine and Surgery, University of Parma, Parma, Italy.
  • Sanchez-Menoyo JL; Department of General Medicine, Parma University Hospital, Parma, Italy.
  • Soysal A; Rehabilitation and MS-Centre Overpelt and Hasselt University, Hasselt, Belgium.
  • Vucic S; Azienda Ospedaliera di Rilievo Nazionale San Giuseppe Moscati Avellino, Avellino, Italy.
  • Petersen T; Flinders University, Adelaide, SA, Australia.
  • de Gans K; University of Queensland, Brisbane, Qld, Australia.
  • Butler E; Royal Brisbane and Women's Hospital, Brisbane, Qld, Australia.
  • Hodgkinson S; CSSS Saint-Jerome, Saint-Jérôme, QC, Canada.
  • Sidhom Y; Nemocnice Jihlava, Jihlava, Czech Republic.
  • Gouider R; Dokuz Eylul University, Konak/Izmir, Turkey.
  • Cristiano E; Hospital de Galdakao-Usansolo, Galdakao, Spain.
  • Castillo-Triviño T; Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.
  • Saladino ML; Westmead Hospital, Sydney, NSW, Australia.
Eur J Neurol ; 29(8): 2321-2334, 2022 08.
Article en En | MEDLINE | ID: mdl-35582938
ABSTRACT
BACKGROUND AND

PURPOSE:

The prevention of disability over the long term is the main treatment goal in multiple sclerosis (MS); however, randomized clinical trials evaluate only short-term treatment effects on disability. This study aimed to define criteria for 6-month confirmed disability progression events of MS with a high probability of resulting in sustained long-term disability worsening.

METHODS:

In total, 14,802 6-month confirmed disability progression events were identified in 8741 patients from the global MSBase registry. For each 6-month confirmed progression event (13,321 in the development and 1481 in the validation cohort), a sustained progression score was calculated based on the demographic and clinical characteristics at the time of progression that were predictive of long-term disability worsening. The score was externally validated in the Cladribine Tablets Treating Multiple Sclerosis Orally (CLARITY) trial.

RESULTS:

The score was based on age, sex, MS phenotype, relapse activity, disability score and its change from baseline, number of affected functional system domains and worsening in six of the domains. In the internal validation cohort, a 61% lower chance of improvement was estimated with each unit increase in the score (hazard ratio 0.39, 95% confidence interval 0.29-0.52; discriminatory index 0.89). The proportions of progression events sustained at 5 years stratified by the score were 1 72%; 2 88%; 3 94%; 4 100%. The results of the CLARITY trial were confirmed for reduction of disability progression that was >88% likely to be sustained (events with score ˃1.5).

CONCLUSIONS:

Clinicodemographic characteristics of 6-month confirmed disability progression events identify those at high risk of sustained long-term disability. This knowledge will allow future trials to better assess the effect of therapy on long-term disability accrual.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Evaluación de la Discapacidad / Esclerosis Múltiple Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Evaluación de la Discapacidad / Esclerosis Múltiple Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Australia