Age and disability accumulation in multiple sclerosis

被引:198
|
作者
Scalfari, A. [1 ]
Neuhaus, A. [2 ]
Daumer, M. [2 ]
Ebers, G. C. [3 ]
Muraro, P. A. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Neurosci, Div Expt Med, London, England
[2] Sylvia Lawry Ctr, Munich, Germany
[3] Univ Oxford, Dept Neurol, Oxford, England
基金
英国医学研究理事会;
关键词
NATURAL-HISTORY; PROGNOSTIC-FACTORS; CLINICAL-COURSE; PROGRESSION; PREDICTORS; RELAPSES;
D O I
10.1212/WNL.0b013e318230a17d
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: We tested the hypothesis that age is a prognostic factor with respect to long-term accumulation of disability in multiple sclerosis (MS). Methods: Kaplan-Meier analysis and binary logistic regression models determined the effect of age at disease onset, age at onset of progression, and current age on attainment of severe disability levels (Disability Status Scale [DSS] 6-8-10) from the London, Ontario, database (n = 1,023). Results: Older age at relapsing-remitting (RR) phase onset was associated with higher risk of reaching advanced DSS scores. This was independent of disease duration and early relapse frequency but secondary to increased risk of conversion to secondary progressive (SP) MS. Onset at age 40 (odds ratio [OR] = 4.22) and at age 50 (OR = 6.04) doubled and tripled risks of developing SP, compared to age 20 (OR = 2.05). Younger age at conversion to SPMS was associated with shorter times to high DSS scores from disease onset. The progressive course, unaffected by age at RR onset, was only modestly affected by age at SP onset. Among primary progressive and RR/SP patients, median ages at attainment of DSS scores were strikingly similar: DSS = 6, 49 vs 48 years; DSS = 8, 58 vs 58 years; and DSS = 10, 78 years for both (p = NS for all comparisons). Conclusions: Development of SP is the dominant determinant of long-term prognosis, independent of disease duration and early relapse frequency. Age independently affects disability development primarily by changing probability and latency of SP onset, with little effect on the progressive course. Neurology (R) 2011; 77: 1246-1252
引用
收藏
页码:1246 / 1252
页数:7
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