Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/27917
Title: Force decline after low and high intensity contractions in persons with multiple sclerosis.
Authors: SEVERIJNS, Deborah 
CUYPERS, Koen 
MEESEN, Raf 
FEYS, Peter 
Zijdewind, Inge
Issue Date: 2019
Source: Clinical neurophysiology, 130 (3), p. 359-367
Abstract: Objective:Force decline during strong contractions is dominated by changes in the periphery whereasduring weaker contraction changes in voluntary activation become more important. We compared forcedecline and contributing factors in persons with multiple sclerosis (PwMS) during low and high intensitycontractions.Methods:Index finger abduction force, force evoked by electrical stimulation of the ulnar nerve at rest(RTw), and during MVCs were investigated in 19 PwMS and 19 controls. Participants performed contrac-tions in sets of six contractions (7 s-on, 3 s-off) at 25% or 80% MVC. After each set, a 5 s-MVC was per-formed with superimposed nerve stimulation followed by RTw. Contractions were repeated until MVCdropped below 80% of initial MVC.Results:Low compared to high intensity contractions caused a greater decline in voluntary activation anda smaller decline in RTw. Compared to controls, PwMS accomplished equal sets of contractions butshowed a smaller decline in RTw. Female PwMS showed poorer voluntary activation. The number oflow intensity contractions was associated with sense of fatigue in PwMS.Conclusion:Although, no difference in fatigability was observed, the mechanism contributing to forcedecline differed between PwMS and controls during submaximal contractions.Significance:During weak contractions, fatigue and fatigability are associated in PwMS.
Notes: Zijdewind, I (reprint author), Hanzepl 1, NL-9700 AD Groningen, Netherlands. c.a.t.zijdewinad@umcg.nl
Keywords: Fatigue; Fatigability; Voluntary activation; Maximal strength; Multiple sclerosis; Superimposed twitch; Sex-related differences
Document URI: http://hdl.handle.net/1942/27917
ISSN: 1388-2457
e-ISSN: 1872-8952
DOI: 10.1016/j.clinph.2018.11.027
ISI #: 000458133100005
Rights: Copyright 2019 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rightsreserved.
Category: A1
Type: Journal Contribution
Validations: ecoom 2020
Appears in Collections:Research publications

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