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Confirmed disability progression as a marker of permanent disability in multiple sclerosis.

Authors :
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
UCL - (SLuc) Service de biochimie médicale
UCL - (SLuc) Service de neurologie
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
Barnett, Michael
Moore, Fraser
Rozsa, Csilla
Yamout, Bassem
Skibina, Olga
van der Walt, Anneke
Buzzard, Katherine
Gray, Orla
Hughes, Stella
Sempere, Angel Perez
Singhal, Bhim
Fragoso, Yara
Shaw, Cameron
Kermode, Allan
Taylor, Bruce
Simo, Magdolna
Shuey, Neil
Al-Harbi, Talal
Macdonell, Richard
Dominguez, Jose Andres
Csepany, Tunde
Sirbu, Carmen Adella
Sormani, Maria Pia
Butzkueven, Helmut
Kalincik, Tomas
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
UCL - (SLuc) Service de biochimie médicale
UCL - (SLuc) Service de neurologie
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
Barnett, Michael
Moore, Fraser
Rozsa, Csilla
Yamout, Bassem
Skibina, Olga
van der Walt, Anneke
Buzzard, Katherine
Gray, Orla
Hughes, Stella
Sempere, Angel Perez
Singhal, Bhim
Fragoso, Yara
Shaw, Cameron
Kermode, Allan
Taylor, Bruce
Simo, Magdolna
Shuey, Neil
Al-Harbi, Talal
Macdonell, Richard
Dominguez, Jose Andres
Csepany, Tunde
Sirbu, Carmen Adella
Sormani, Maria Pia
Butzkueven, Helmut
Kalincik, Tomas
Source :
European journal of neurology, Vol. 154, no.06, p. 1-14 (2022)
Publication Year :
2022

Abstract

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. 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. 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). 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.

Details

Database :
OAIster
Journal :
European journal of neurology, Vol. 154, no.06, p. 1-14 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372953413
Document Type :
Electronic Resource