Treatment of walking impairment in multiple sclerosis: an unmet need for a disease-specific disability

被引:16
作者
Panitch, Hillel [1 ]
Applebee, Angela [1 ]
机构
[1] Univ Vermont, Coll Med, Neurol Serv, Burlington, VT 05401 USA
关键词
activities of daily living; dalfampridine; demyelination; disability; immunomodulators; multiple sclerosis; neurofunctional modifiers; potassium channel blocker; quality of life; walking impairment; QUALITY-OF-LIFE; SPINAL-CORD-INJURY; DOUBLE-BLIND; 4-AMINOPYRIDINE TOXICITY; SYMPTOMATIC TREATMENT; FUNCTIONAL COMPOSITE; MODIFYING THERAPIES; AXONAL CONDUCTION; CLINICAL SIGNS; LONG-TERM;
D O I
10.1517/14656566.2011.586338
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Walking impairment is a clinical hallmark of multiple sclerosis (MS), a chronic neurologic disease characterized by axonal demyelination and dysfunction that results in progressive disability. Until recently, there were no therapies that specifically targeted the axonal dysfunction associated with walking impairment in MS. Areas covered: The purpose of this review is to discuss the unmet need for the treatment of walking impairment in MS patients and to evaluate how a new class of pharmacologic therapies, neurofunctional modifiers, potentially addresses this unmet need. Discussion is based on clinical experience and opinions supported by publications identified in the PubMed literature using the search terms 'multiple sclerosis' and 'mobility OR walking'. Expert opinion: The development and approval of new treatments for MS show promise for improving adherence to therapy and increasing the potential for clinical effectiveness. Renewed emphasis on integrating strategies that target the underlying pathophysiology with those that address symptoms of concern to patients also has the potential to improve the lives of MS patients and their caregivers. The introduction of neurofunctional modifiers, such as dalfampridine for the improvement of walking impairment, may be of benefit by improving function, mobility and overall quality of life for MS patients.
引用
收藏
页码:1511 / 1521
页数:11
相关论文
共 101 条
[21]   Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability [J].
De Stefano, N ;
Narayanan, S ;
Francis, GS ;
Arnaoutelis, R ;
Tartaglia, MC ;
Antel, JP ;
Matthews, PM ;
Arnold, DL .
ARCHIVES OF NEUROLOGY, 2001, 58 (01) :65-70
[22]  
DUNN J, CURR MED RE IN PRESS
[23]   Cognitive and motor function in people with multiple sclerosis in Stockholm County [J].
Einarsson, U ;
Gottberg, K ;
Von Koch, L ;
Fredrikson, S ;
Ytterberg, C ;
Jin, YP ;
Andersson, M ;
Holmqvist, LW .
MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (03) :340-353
[24]   Efficacy of disease-modifying therapies in relapsing remitting multiple sclerosis: A systematic comparison [J].
Freedman, Mark S. ;
Hughes, Bruce ;
Mikol, Daniel D. ;
Bennett, Randy ;
Cuffel, Brian ;
Divan, Vamil ;
LaVallee, Nicole ;
Al-Sabbagh, Ahmad .
EUROPEAN NEUROLOGY, 2008, 60 (01) :1-11
[25]   Most patients with multiple sclerosis or a clinically isolated demyelinating syndrome should be treated at the time of diagnosis [J].
Frohman, EM ;
Havrdova, E ;
Lublin, F ;
Barkhof, F ;
Achiron, A ;
Sharief, MK ;
Stuve, O ;
Racke, MK ;
Steinman, L ;
Weiner, H ;
Olek, M ;
Zivadinov, R ;
Corboy, J ;
Raine, C ;
Cutter, G ;
Richert, J ;
Filippi, M .
ARCHIVES OF NEUROLOGY, 2006, 63 (04) :614-619
[26]   Disease modifying therapies in multiple sclerosis - Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines [J].
Goodin, DS ;
Frohman, EM ;
Garmany, GP ;
Halper, J ;
Likosky, WH ;
Lublin, FD ;
Silberberg, DH ;
Stuart, WH ;
van den Noort, S .
NEUROLOGY, 2002, 58 (02) :169-178
[27]  
GOODMAN A, 2010, MULT SCLER, V16, pS17
[28]   Dose comparison trial of sustained-release fampridine in multiple sclerosis [J].
Goodman, A. D. ;
Brown, T. R. ;
Cohen, J. A. ;
Krupp, L. B. ;
Schapiro, R. ;
Schwid, S. R. ;
Cohen, R. ;
Marinucci, L. N. ;
Blight, A. R. .
NEUROLOGY, 2008, 71 (15) :1134-1141
[29]   Fampridine-SR in multiple sclerosis: a randomized, double-blind, placebo-controlled, dose-ranging study [J].
Goodman, A. D. ;
Cohen, J. A. ;
Cross, A. ;
Vollmer, T. ;
Rizzo, M. ;
Cohen, R. ;
Marinucci, L. ;
Blight, A. R. .
MULTIPLE SCLEROSIS, 2007, 13 (03) :357-368
[30]   A Phase 3 Trial of Extended Release Oral Dalfampridine in Multiple Sclerosis [J].
Goodman, Andrew D. ;
Brown, Theodore R. ;
Edwards, Keith R. ;
Krupp, Lauren B. ;
Schapiro, Randall T. ;
Cohen, Ron ;
Marinucci, Lawrence N. ;
Blight, Andrew R. .
ANNALS OF NEUROLOGY, 2010, 68 (04) :494-502