Motor fatigue is a common complaint in patients with amyotrophic, lateral s
clerosis (ALS), but is often excluded, unlike weakness, from the clinical a
ssessment of these patients. This could be due to the complexity and often
painful assessment techniques of this motor deficit. This study examines th
e feasibility of quantitative assessment of motor fatigue by modifying pres
ently available force measurements. The relationship between weakness and f
atigue in ALS patients was also examined. Fifty-four ALS patients and 39 no
rmal control subjects performed 30 s. of sustained maximal voluntary isomet
ric contraction (MVIC) of elbow flexors (EF), knee extensors (NE), and ankl
e dorsiflexors (DF), using a computerized force measurement system and stan
dardized testing procedures. Fatigue index (FI) was digitally calculated, f
rom the force-time curve, as the percentage of MVIC unable to be sustained
over the 30-s period. Fatigue was greater in ALS patients than in normal co
ntrol (mean = 23% vs. 15%) in all muscles including muscles that were not c
learly weak. Weakness and fatigue were poorly correlated in ALS patients an
d may be independent measures of the pathogeneses of ALS. (C) 2001 Elsevier
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