Prediction of long-term disability in multiple sclerosis

被引:40
|
作者
Schlaeger, R. [1 ]
D'Souza, M. [1 ]
Schindler, C. [3 ]
Grize, L. [3 ]
Dellas, S. [2 ]
Radue, E. W. [2 ]
Kappos, L. [1 ]
Fuhr, P. [1 ]
机构
[1] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Neuroradiol, CH-4031 Basel, Switzerland
[3] Univ Basel, Swiss Trop & Publ Hlth Inst, CH-4003 Basel, Switzerland
关键词
evoked potentials; multiple sclerosis; prognosis; CLINICALLY ISOLATED SYNDROMES; MULTIMODAL EVOKED-POTENTIALS; 10-YEAR FOLLOW-UP; BRAIN MRI; PROGRESSION; ABNORMALITIES; EVOLUTION; LESIONS; TRIALS;
D O I
10.1177/1352458511416836
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Little is known about the predictive value of neurophysiological measures for the long-term course of multiple sclerosis (MS). Objective: To prospectively investigate whether combined visual (VEP) and motor evoked potentials (MEP) allow prediction of disability over 14 years. Methods: A total of 30 patients with relapsing-remitting and secondary progressive MS were prospectively investigated with VEPs, MEPs and the Expanded Disability Status Scale (EDSS) at entry (T0) and after 6, 12 and 24 months, and with cranial MRI scans at entry (T2-weighted and gadolinium-enhanced T1-weighted images). EDSS was again assessed at year 14 (T4). The association between evoked potential (EP), magnetic resonance (MR) data and EDSS was measured using Spearman's rank correlation. Multivariable linear regression was performed to predict EDSST4 as a function of z-transformed EP-latencies(T0). The model was validated using a jack-knife procedure and the potential for improving it by inclusion of additional baseline variables was examined. Results: EDSS values(T4) correlated with the sum of z-transformed EP-latencies(T0) (rho 0.68, p<0.0001), but not with MR-parameters(T0). EDSST4 as predicted by the formula EDSST4 4.194_0.088* z-score P100(T0)+0.071 * z-score CMCTUE, (T0) correlated with the observed values (rho=0.69, p<0.0001). Conclusion: Combined EPs allow prediction of long-term disability in small groups of patients with MS. This may have implications for the choice of monitoring methods in clinical trials and for daily practice decisions.
引用
收藏
页码:31 / 38
页数:8
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