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
[51]   Clinical impact of 20% worsening on Timed 25-foot Walk and 9-hole Peg Test in multiple sclerosis [J].
Kragt, J. J. ;
van der Linden, F. A. H. ;
Nielsen, J. M. ;
Uitdehaag, B. M. J. ;
Polman, C. H. .
MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (05) :594-598
[52]  
KURTZKE JF, 1983, NEUROLOGY, V33, P1444, DOI 10.1212/WNL.33.11.1444
[53]   EFFECTS OF 4-AMINOPYRIDINE IN MYASTHENIA-GRAVIS [J].
LUNDH, H ;
NILSSON, O ;
ROSEN, I .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1979, 42 (02) :171-175
[54]   EFFECTS OF 4-AMINOPYRIDINE ON NEUROMUSCULAR-TRANSMISSION [J].
LUNDH, H .
BRAIN RESEARCH, 1978, 153 (02) :307-318
[55]   4-AMINOPYRIDINE - NEW DRUG TESTED IN TREATMENT OF EATON-LAMBERT SYNDROME [J].
LUNDH, H ;
NILSSON, O ;
ROSEN, I .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1977, 40 (11) :1109-1112
[56]   Validity of performance scales for disability assessment in multiple sclerosis [J].
Marrie, R. A. ;
Goldman, M. .
MULTIPLE SCLEROSIS JOURNAL, 2007, 13 (09) :1176-1182
[57]   Gait and balance impairment in early multiple sclerosis in the absence of clinical disability [J].
Martin, C. L. ;
Phillips, B. A. ;
Kilpatrick, T. J. ;
Butzkueven, H. ;
Tubridy, N. ;
McDonald, E. ;
Galea, M. P. .
MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (05) :620-628
[58]  
MILLER AE, 2000, MSQR MULTIPLE SCLERO, V19, P7
[59]   Primary-progressive multiple sclerosis (vol 6, pg 903, 2007) [J].
Miller, D. ;
Leary, S. M. .
LANCET NEUROLOGY, 2009, 8 (08) :699-699
[60]   A DOUBLE-BLIND CONTROLLED TRIAL OF HIGH-DOSE METHYLPREDNISOLONE IN PATIENTS WITH MULTIPLE-SCLEROSIS .1. CLINICAL EFFECTS [J].
MILLIGAN, NM ;
NEWCOMBE, R ;
COMPSTON, DAS .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (05) :511-516