Learning ability correlates with brain atrophy and disability progression in RRMS

被引:16
作者
Sormani, Maria Pia [1 ]
De Stefano, Nicola [2 ]
Giovannoni, Gavin [3 ]
Langdon, Dawn [4 ]
Piani-Meier, Daniela [5 ]
Haering, Dieter A. [5 ]
Kappos, Ludwig [6 ,7 ,8 ]
Tomic, Davorka [5 ]
机构
[1] Univ Genoa, Dept Hlth Sci, Biostat Unit, I-16126 Genoa, Italy
[2] Univ Siena, Dept Med Surg & Neurosci, Siena, Italy
[3] Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England
[4] Royal Holloway Univ London, Dept Psychol, Egham, Surrey, England
[5] Novartis Pharma AG, Basel, Switzerland
[6] Univ Basel, Univ Hosp Basel, Neurol Clin & Polyclin, Dept Med, Basel, Switzerland
[7] Univ Basel, Univ Hosp Basel, Neurol Clin & Polyclin, Dept Clin Res, Basel, Switzerland
[8] Univ Basel, Univ Hosp Basel, Neurol Clin & Polyclin, Dept Biomed & Biomed Engn, Basel, Switzerland
基金
新加坡国家研究基金会;
关键词
SERIAL ADDITION TEST; MULTIPLE-SCLEROSIS; COGNITIVE IMPAIRMENT; FUNCTIONAL COMPOSITE; VOLUME LOSS; EARLY-STAGE; RESERVE; FINGOLIMOD; MS;
D O I
10.1136/jnnp-2018-319129
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To assess the prognostic value of practice effect on Paced Auditory Serial Addition Test (PASAT) in multiple sclerosis. Methods We compared screening (day - 14) and baseline (day 0) PASAT scores of 1009 patients from the FTY720 Research Evaluating Effects of Daily Oral therapy in Multiple Sclerosis (FREEDOMS) trial. We grouped patients into high and low learners if their PASAT score change was above or below the median change in their screening PASAT quartile group. We used Wilcoxon test to compare baseline disease characteristics between high and low learners, and multiple regression models to assess the respective impact of learning ability, baseline normalised brain volume and treatment on brain volume loss and 6-month confirmed disability progression over 2 years. Results The mean PASAT score at screening was 45.38, increasing on average by 3.18 from day -14 to day 0. High learners were younger (p=0.003), had lower Expanded Disability Status Scale score (p=0.031), higher brain volume (p<0.001) and lower T2 lesion volume (p=0.009) at baseline. Learning status was not significantly associated with disability progression (HR=0.953, p=0.779), when adjusting for baseline normalised brain volume, screening PASAT score and treatment arm. However, the effect of fingolimod on disability progression was more pronounced in high learners (HR=0.396, p<0.001) than in low learners (HR=0.798, p=0.351; p for interaction=0.05). Brain volume loss at month 24 tended to be higher in low learners (0.17%, p=0.058), after adjusting for the same covariates. Conclusions Short-term practice effects on PASAT are related to brain volume, disease severity and age and have clinically meaningful prognostic implications. High learners benefited more from fingolimod treatment.
引用
收藏
页码:38 / 43
页数:6
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