Early predictors of disability in paediatric multiple sclerosis: evidence from a multi-national registry

医学 扩大残疾状况量表 多发性硬化 儿科 四分位数 内科学 物理疗法 置信区间 精神科
作者
Sifat Sharmin,Charles B. Malpas,Izanne Roos,Ibrahima Diouf,Raed Alroughani,Serkan Özakbaş,Guillermo Izquierdo,Sara Eichau,Dana Horáková,Eva Havrdová,Francesco Patti,Murat Terzi,Cavit Boz,Bassem Yamout,Samia J. Khoury,Marco Onofrj,Alessandra Lugaresi,Ayşe Altıntaş,Alexandre Prat,Marc Girard,Pierre Duquette,María José Sá,Daniele Spitaleri,Youssef Sidhom,Riadh Gouider,Saloua Mrabet,Aysun Soysal,Recai Türkoğlu,Maria Pia Amato,Yára Dadalti Fragoso,Tomáš Kalinčík
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:: jnnp-329713 被引量:1
标识
DOI:10.1136/jnnp-2022-329713
摘要

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.

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