Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy

Research output: Contribution to journalJournal articleResearchpeer-review

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Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy. / Geertsen, Svend Sparre; Kirk, Henrik; Nielsen, Jens Bo.

In: Neural Plasticity, Vol. 2018, 1265143, 2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Geertsen, SS, Kirk, H & Nielsen, JB 2018, 'Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy', Neural Plasticity, vol. 2018, 1265143. https://doi.org/10.1155/2018/1265143

APA

Geertsen, S. S., Kirk, H., & Nielsen, J. B. (2018). Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy. Neural Plasticity, 2018, [1265143]. https://doi.org/10.1155/2018/1265143

Vancouver

Geertsen SS, Kirk H, Nielsen JB. Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy. Neural Plasticity. 2018;2018. 1265143. https://doi.org/10.1155/2018/1265143

Author

Geertsen, Svend Sparre ; Kirk, Henrik ; Nielsen, Jens Bo. / Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy. In: Neural Plasticity. 2018 ; Vol. 2018.

Bibtex

@article{9cbe5b59cc0b4f288400e2a004e31b5c,
title = "Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy",
abstract = "We recently showed that impaired gait function in adults with cerebral palsy (CP) is associated with reduced rate of force development in ankle dorsiflexors. Here, we explore potential mechanisms. We investigated the suppression of antagonist excitability, calculated as the amount of soleus H-reflex depression at the onset of ankle dorsiflexion compared to rest, in 24 adults with CP (34.3 years, range 18–57; GMFCS 1.95, range 1–3) and 15 healthy, age-matched controls. Furthermore, the central common drive to dorsiflexor motoneurons during a static contraction in the two groups was examined by coherence analyses. The H-reflex was significantly reduced by 37% at the onset of dorsiflexion compared to rest in healthy adults (P < 0.001) but unchanged in adults with CP (P = 0.91). Also, the adults with CP had significantly less coherence. These findings suggest that the ability to suppress antagonist motoneuronal excitability at movement onset is impaired and that the central common drive during static contractions is reduced in adults with CP.",
keywords = "Adolescent, Adult, Cerebral Palsy/diagnosis, Electromyography/methods, Female, H-Reflex/physiology, Humans, Male, Middle Aged, Motor Neurons/physiology, Muscle, Skeletal/physiopathology, Range of Motion, Articular/physiology, Reaction Time/physiology, Young Adult",
author = "Geertsen, {Svend Sparre} and Henrik Kirk and Nielsen, {Jens Bo}",
note = "CURIS 2018 NEXS 348",
year = "2018",
doi = "10.1155/2018/1265143",
language = "English",
volume = "2018",
journal = "Neural Plasticity",
issn = "2090-5904",
publisher = "Hindawi Publishing Corporation",

}

RIS

TY - JOUR

T1 - Impaired Ability to Suppress Excitability of Antagonist Motoneurons at Onset of Dorsiflexion in Adults with Cerebral Palsy

AU - Geertsen, Svend Sparre

AU - Kirk, Henrik

AU - Nielsen, Jens Bo

N1 - CURIS 2018 NEXS 348

PY - 2018

Y1 - 2018

N2 - We recently showed that impaired gait function in adults with cerebral palsy (CP) is associated with reduced rate of force development in ankle dorsiflexors. Here, we explore potential mechanisms. We investigated the suppression of antagonist excitability, calculated as the amount of soleus H-reflex depression at the onset of ankle dorsiflexion compared to rest, in 24 adults with CP (34.3 years, range 18–57; GMFCS 1.95, range 1–3) and 15 healthy, age-matched controls. Furthermore, the central common drive to dorsiflexor motoneurons during a static contraction in the two groups was examined by coherence analyses. The H-reflex was significantly reduced by 37% at the onset of dorsiflexion compared to rest in healthy adults (P < 0.001) but unchanged in adults with CP (P = 0.91). Also, the adults with CP had significantly less coherence. These findings suggest that the ability to suppress antagonist motoneuronal excitability at movement onset is impaired and that the central common drive during static contractions is reduced in adults with CP.

AB - We recently showed that impaired gait function in adults with cerebral palsy (CP) is associated with reduced rate of force development in ankle dorsiflexors. Here, we explore potential mechanisms. We investigated the suppression of antagonist excitability, calculated as the amount of soleus H-reflex depression at the onset of ankle dorsiflexion compared to rest, in 24 adults with CP (34.3 years, range 18–57; GMFCS 1.95, range 1–3) and 15 healthy, age-matched controls. Furthermore, the central common drive to dorsiflexor motoneurons during a static contraction in the two groups was examined by coherence analyses. The H-reflex was significantly reduced by 37% at the onset of dorsiflexion compared to rest in healthy adults (P < 0.001) but unchanged in adults with CP (P = 0.91). Also, the adults with CP had significantly less coherence. These findings suggest that the ability to suppress antagonist motoneuronal excitability at movement onset is impaired and that the central common drive during static contractions is reduced in adults with CP.

KW - Adolescent

KW - Adult

KW - Cerebral Palsy/diagnosis

KW - Electromyography/methods

KW - Female

KW - H-Reflex/physiology

KW - Humans

KW - Male

KW - Middle Aged

KW - Motor Neurons/physiology

KW - Muscle, Skeletal/physiopathology

KW - Range of Motion, Articular/physiology

KW - Reaction Time/physiology

KW - Young Adult

U2 - 10.1155/2018/1265143

DO - 10.1155/2018/1265143

M3 - Journal article

C2 - 30402086

VL - 2018

JO - Neural Plasticity

JF - Neural Plasticity

SN - 2090-5904

M1 - 1265143

ER -

ID: 203561248