TY - JOUR
T1 - Early predictors of disability in paediatric multiple sclerosis
T2 - evidence from a multi-national registry
AU - Sharmin, Sifat
AU - Malpas, Charles B.
AU - Roos, Izanne
AU - Diouf, Ibrahima
AU - Alroughani, Raed
AU - Ozakbas, Serkan
AU - Izquierdo, Guillermo
AU - Eichau, Sara
AU - Horakova, Dana
AU - Havrdova, Eva K.
AU - Patti, Francesco
AU - Terzi, Murat
AU - Boz, Cavit
AU - Yamout, Bassem
AU - Khoury, Samia J.
AU - Onofrj, Marco
AU - Lugaresi, Alessandra
AU - Altintas, Ayse
AU - Prat, Alexandre
AU - Girard, Marc
AU - Duquette, Pierre
AU - Sá, Maria José
AU - La Spitaleri, Daniele
AU - Sidhom, Youssef
AU - Gouider, Riadh
AU - Mrabet, Saloua
AU - Soysal, Aysun
AU - Turkoglu, Recai
AU - Amato, Maria Pia
AU - Fragoso, Yara D.
AU - Kalincik, Tomas
N1 - Funding Information:
This study was funded by the NHMRC Australia (grant 1129189 and fellowship 1140766). The MSBase Foundation is a not-for-profit organisation that receives support from Merck, Biogen, Novartis, Roche, Bayer Schering, Sanofi Genzyme and Teva Pharmaceutical Industries.
Publisher Copyright:
© 2022 BMJ Publishing Group. All rights reserved.
PY - 2022/9/30
Y1 - 2022/9/30
N2 - Background Early recognition of markers of faster disability worsening in paediatric-onset multiple sclerosis (MS) is a key requisite of personalised therapy for children with MS at the earliest possible time. Objective To identify early predictors of rapid disability accrual in patients with paediatric-onset MS. Methods Using the global MSBase registry, we identified patients who were <18 years old at the onset of MS symptoms. The clinico-demographic characteristics examined as predictors of future MS Severity Score (MSSS) included sex, age at symptom onset, absence of disability at the initial assessment, maximum Expanded Disability Status Scale (EDSS) score, relapse frequency and presence of brainstem, pyramidal, visual or cerebellar symptoms in the first year. A Bayesian log-normal generalised linear mixed model adjusted for cumulative proportion of time on higher-efficacy disease-modifying therapies (DMTs) was used to analyse the data. Results 672 patients (70% female) contributing 9357 visits were included. The median age at symptom onset was 16 (quartiles 15-17) years. Older age at symptom onset (exp(β)=1.10 (95% CI 1.04 to 1.17)), higher EDSS score (1.22 (1.12 to 1.34)) and pyramidal (1.31 (1.11 to 1.55)), visual (1.25 (1.10 to 1.44)) or cerebellar (1.18 (1.01 to 1.38)) symptoms in the first year were associated with higher MSSS. MSSS was reduced by 4% for every 24% increase in the proportion of time on higher-efficacy DMTs (0.96 (0.93 to 0.99)). Conclusions A relatively later onset of MS in childhood, higher disability and pyramidal, visual or cerebellar symptoms during the first year predicted significant worsening in disability in patients with paediatric-onset MS. Persistent treatment with higher-efficacy DMTs was associated with a reduced rate of disability worsening.
AB - Background Early recognition of markers of faster disability worsening in paediatric-onset multiple sclerosis (MS) is a key requisite of personalised therapy for children with MS at the earliest possible time. Objective To identify early predictors of rapid disability accrual in patients with paediatric-onset MS. Methods Using the global MSBase registry, we identified patients who were <18 years old at the onset of MS symptoms. The clinico-demographic characteristics examined as predictors of future MS Severity Score (MSSS) included sex, age at symptom onset, absence of disability at the initial assessment, maximum Expanded Disability Status Scale (EDSS) score, relapse frequency and presence of brainstem, pyramidal, visual or cerebellar symptoms in the first year. A Bayesian log-normal generalised linear mixed model adjusted for cumulative proportion of time on higher-efficacy disease-modifying therapies (DMTs) was used to analyse the data. Results 672 patients (70% female) contributing 9357 visits were included. The median age at symptom onset was 16 (quartiles 15-17) years. Older age at symptom onset (exp(β)=1.10 (95% CI 1.04 to 1.17)), higher EDSS score (1.22 (1.12 to 1.34)) and pyramidal (1.31 (1.11 to 1.55)), visual (1.25 (1.10 to 1.44)) or cerebellar (1.18 (1.01 to 1.38)) symptoms in the first year were associated with higher MSSS. MSSS was reduced by 4% for every 24% increase in the proportion of time on higher-efficacy DMTs (0.96 (0.93 to 0.99)). Conclusions A relatively later onset of MS in childhood, higher disability and pyramidal, visual or cerebellar symptoms during the first year predicted significant worsening in disability in patients with paediatric-onset MS. Persistent treatment with higher-efficacy DMTs was associated with a reduced rate of disability worsening.
KW - multiple sclerosis
KW - neuroepidemiology
KW - neuroimmunology
KW - paediatric neurology
UR - https://www.scopus.com/pages/publications/85142519333
U2 - 10.1136/jnnp-2022-329713
DO - 10.1136/jnnp-2022-329713
M3 - Article
C2 - 36180218
AN - SCOPUS:85142519333
SN - 0022-3050
VL - 93
SP - 1322
EP - 1329
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 12
ER -