In-Vivo Study of Passive Musculotendon Mechanics in Chronic Hemispheric Stroke Survivors.
Journal
IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society
ISSN: 1558-0210
Titre abrégé: IEEE Trans Neural Syst Rehabil Eng
Pays: United States
ID NLM: 101097023
Informations de publication
Date de publication:
04 2020
04 2020
Historique:
pubmed:
10
3
2020
medline:
25
6
2021
entrez:
10
3
2020
Statut:
ppublish
Résumé
We characterized the passive mechanical properties of the affected and contralateral musculotendon units in 9 chronic stroke survivors as well as in 6 neurologically-intact controls. Using a position-controlled motor, we precisely indented the distal tendon of the biceps brachii to a 20 mm depth from skin, recording both its sagittal motion using ultrasound movies and the compression force at the tip of the indenter. Length changes of 8 equally-spaced features along the aponeurosis axis were quantified using a pixel-tracking protocol. We report that, on the aggregate and with respect to contralateral and control, respectively, the affected side initiates feature motion at a shorter indentation distance by 61% and 50%, travels further by 15% and 9%, at a lower rate of 28% and 15%, and is stiffer by 40% and 57%. In an extended analysis including the spatial location of the 8 designated features, we report that in contrast to the contralateral and control muscles, the affected musculotendon unit does not strain measurably within the imaging window. These results confirm that chronic stroke-induced spasticity changes musculotendon unit passive mechanics, causing it to not strain under stretch. The mechanisms responsible for altered passive mechanics may lie within extracellular matrix fibrosis.
Identifiants
pubmed: 32149642
doi: 10.1109/TNSRE.2020.2972206
pmc: PMC7233468
mid: NIHMS1583798
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1022-1031Subventions
Organisme : NICHD NIH HHS
ID : R01 HD089952
Pays : United States
Organisme : NICHD NIH HHS
ID : R24 HD050821
Pays : United States
Références
Arch Phys Med Rehabil. 2004 Oct;85(10):1631-7
pubmed: 15468023
Phys Ther. 1987 Feb;67(2):206-7
pubmed: 3809245
Clin Biomech (Bristol, Avon). 2000 May;15(4):261-70
pubmed: 10675667
Am J Physiol Cell Physiol. 2013 Aug 1;305(3):C241-52
pubmed: 23761627
J Biomech Eng. 2002 Feb;124(1):72-7
pubmed: 11871607
Proc R Soc Lond B Biol Sci. 1972 Mar 14;180(1060):293-315
pubmed: 4402469
Clin Biomech (Bristol, Avon). 2015 Mar;30(3):269-75
pubmed: 25638688
J Biomech Eng. 1998 Dec;120(6):757-63
pubmed: 10412460
J Biomech. 2015 Oct 15;48(13):3568-76
pubmed: 26321363
J Neurophysiol. 2011 May;105(5):2132-49
pubmed: 21346215
J Appl Physiol (1985). 2011 Nov;111(5):1491-6
pubmed: 21836045
Arch Phys Med Rehabil. 2004 Oct;85(10):1638-46
pubmed: 15468024
J Appl Physiol (1985). 2009 Mar;106(3):843-9
pubmed: 19118156
Muscle Nerve. 2005 May;31(5):552-71
pubmed: 15714511
J Orthop Res. 2009 Dec;27(12):1596-602
pubmed: 19544524
Arch Phys Med Rehabil. 2009 May;90(5):819-26
pubmed: 19406302
Arch Phys Med Rehabil. 2007 Feb;88(2):243-50
pubmed: 17270524
Ageing Res Rev. 2018 Nov;47:123-132
pubmed: 30048806
IEEE Trans Neural Syst Rehabil Eng. 2014 Mar;22(2):280-9
pubmed: 24621852
J Muscle Res Cell Motil. 2002;23(3):245-54
pubmed: 12500904
Brain. 1994 Apr;117 ( Pt 2):355-63
pubmed: 8186961
Muscle Nerve. 2015 Oct;52(4):649-57
pubmed: 25598004
Clin Neurophysiol. 2010 Nov;121(11):1939-51
pubmed: 20457538
Practitioner. 1964 Apr;192:540-2
pubmed: 14143329
J Neurophysiol. 2007 Aug;98(2):629-37
pubmed: 17537910
Conf Proc IEEE Eng Med Biol Soc. 2010;2010:2993-6
pubmed: 21095718
Acta Biomater. 2013 Nov;9(11):9036-48
pubmed: 23811521