Neuromuscular control during gait in people with haemophilic arthropathy.


Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 09 12 2018
revised: 20 01 2019
accepted: 21 01 2019
pubmed: 13 2 2019
medline: 30 4 2019
entrez: 13 2 2019
Statut: ppublish

Résumé

Effects of haemophilic arthropathy on neuromuscular control during gait are currently unknown. (a) To assess how haemophilic arthropathy affects the complexity of neuromuscular control during gait; (b) To investigate the relationship between complexity of neuromuscular control and joint impairment. Thirteen control subjects (CG) walked overground at their preferred and a slow velocity and thirteen people with haemophilic arthropathy (PWHA) walking at their preferred velocity. Surface electromyography (EMG) was collected from eleven leg muscles. Electromyography variance explained by muscle synergies (sets of co-activated muscles that can be recruited by a single signal) was calculated by the total variance accounted (tVAF). Three measures were used to evaluate complexity of neuromuscular control: (a) the number of synergies required for tVAF > 90%, (b) tVAF as a function of the number of muscle synergies, and (c) the dynamic motor control index (Walk-DMC). Impairment of ankle and knee joints was determined by the Haemophilia Joint Health Score (HJHS). The same number of the muscle synergies was found for each group (P > 0.05). For both walking velocities tested, tVAF1 was higher in PHWA (P < 0.05). The Walk-DMC of PWHA was lower than that of the CG for both walking velocities (P < 0.05). For PWHA, no significant correlation was found between HJHS (sum knee and ankle) and Walk-DMC index (r = -0.32, P = 0.28). These results indicate differences between PWHA and CG in the neuromuscular control of gait. The Walk-DMC and tVAF1 may be useful measures to assess changes in neuromuscular control in response to treatment.

Identifiants

pubmed: 30748060
doi: 10.1111/hae.13697
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e69-e77

Subventions

Organisme : FONDECYT
ID : 11161033
Organisme : FONDEQUIP
ID : EQM140119
Organisme : FONDEQUIP
ID : ACT1402
Organisme : FONDEQUIP
ID : P09-015-F

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Auteurs

Carlos Cruz-Montecinos (C)

Department of Physiotherapy, University of Valencia, Valencia, Spain.
Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences, Amsterdam Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Laboratory of Clinical Biomechanics, Department of Physical Therapy, Faculty of Medicine, University of Chile, Santiago, Chile.

Sofía Pérez-Alenda (S)

Department of Physiotherapy, University of Valencia, Valencia, Spain.

Mauricio Cerda (M)

SCIAN-Lab, Programme of Anatomy and Developmental Biology, Faculty of Medicine, ICBM, University of Chile, Santiago, Chile.

Huub Maas (H)

Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences, Amsterdam Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

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