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- W2911541619 abstract "Voluntary toe walking in adults is characterized by feedforward control of ankle muscles in order to ensure optimal stability of the ankle joint at ground impact. Toe walking is frequently observed in children with cerebral palsy, but the mechanisms involved have not been clarified. Here, we investigated maturation of voluntary toe walking in typically-developing children and typically-developed adults and compared it to involuntary toe walking in children with cerebral palsy. Twenty-eight children with cerebral palsy (age 3-14 years), 24 typically-developing children (age 2-14 years) and 15 adults (mean age 30.7 years) participated in the study. EMG activity was measured from the tibialis anterior and soleus muscles together with knee and ankle joint position during treadmill walking. In typically-developed adults, low step-to-step variability of the drop of the heel after ground impact was correlated with low tibialis anterior and high soleus EMG with no significant coupling between the antagonist muscle EMGs. Typically-developing children showed a significant age-related decline in EMG amplitude reaching an adult level at 10-12 years of age. The youngest typically-developing children showed a broad peak EMG-EMG synchronization (>100 ms) associated with large 5-15 Hz coherence between antagonist muscle activities. EMG coherence declined with age and at the age of 10-12 years no correlation was observed similar to adults. This reduction in coherence was closely related to improved step-to-step stability of the ankle joint position. Children with cerebral palsy generally showed lower EMG levels than typically-developing children and larger step-to-step variability in ankle joint position. In contrast to typically-developing children, children with cerebral palsy showed no age-related decline in tibialis anterior EMG amplitude. Motor unit synchronization and 5-15 Hz coherence between antagonist EMGs was observed more frequently in children with cerebral palsy when compared to typically-developing children and in contrast to typically-developing participants there was no age-related decline. We conclude that typically-developing children develop mature feedforward control of ankle muscle activity as they age, such that at age 10-12 years there is little agonist-antagonist muscle co-contraction around the time of foot-ground contact during toe walking. Children with cerebral palsy, in contrast, continue to co-contract agonist and antagonist ankle muscles when toe walking. We speculate that children with cerebral palsy maintain a co-contraction activation pattern when toe walking due to weak muscles and insufficient motor and sensory signalling necessary for optimization of feedforward motor programs. These findings are important for understanding of the pathophysiology and treatment of toe walking." @default.
- W2911541619 created "2019-02-21" @default.
- W2911541619 creator A5024297961 @default.
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- W2911541619 creator A5089358060 @default.
- W2911541619 date "2019-02-04" @default.
- W2911541619 modified "2023-10-12" @default.
- W2911541619 title "Maturation of feedforward toe walking motor program is impaired in children with cerebral palsy" @default.
- W2911541619 cites W1531808741 @default.
- W2911541619 cites W1568832828 @default.
- W2911541619 cites W1569163094 @default.
- W2911541619 cites W1838602924 @default.
- W2911541619 cites W1919222771 @default.
- W2911541619 cites W1967397213 @default.
- W2911541619 cites W1967797382 @default.
- W2911541619 cites W1970890515 @default.
- W2911541619 cites W1974611073 @default.
- W2911541619 cites W1975312229 @default.
- W2911541619 cites W1977662996 @default.
- W2911541619 cites W1978682876 @default.
- W2911541619 cites W1980641959 @default.
- W2911541619 cites W1981578159 @default.
- W2911541619 cites W1981818123 @default.
- W2911541619 cites W1984417136 @default.
- W2911541619 cites W1984643334 @default.
- W2911541619 cites W1984742350 @default.
- W2911541619 cites W1991312711 @default.
- W2911541619 cites W1999735388 @default.
- W2911541619 cites W1999879638 @default.
- W2911541619 cites W2002115993 @default.
- W2911541619 cites W2003209004 @default.
- W2911541619 cites W2004647625 @default.
- W2911541619 cites W2009473852 @default.
- W2911541619 cites W2010340475 @default.
- W2911541619 cites W2010983048 @default.
- W2911541619 cites W2012979514 @default.
- W2911541619 cites W2016519054 @default.
- W2911541619 cites W2021556358 @default.
- W2911541619 cites W2023832737 @default.
- W2911541619 cites W2024376631 @default.
- W2911541619 cites W2042816348 @default.
- W2911541619 cites W2050687519 @default.
- W2911541619 cites W2050708439 @default.
- W2911541619 cites W2052198872 @default.
- W2911541619 cites W2053133492 @default.
- W2911541619 cites W2055426605 @default.
- W2911541619 cites W2056556983 @default.
- W2911541619 cites W2056761616 @default.
- W2911541619 cites W2066273235 @default.
- W2911541619 cites W2068096613 @default.
- W2911541619 cites W2068496090 @default.
- W2911541619 cites W2070010556 @default.
- W2911541619 cites W2072921322 @default.
- W2911541619 cites W2073169940 @default.
- W2911541619 cites W2080487795 @default.
- W2911541619 cites W2089151651 @default.
- W2911541619 cites W2089572228 @default.
- W2911541619 cites W2092395878 @default.
- W2911541619 cites W2096291680 @default.
- W2911541619 cites W2096420372 @default.
- W2911541619 cites W2097751995 @default.
- W2911541619 cites W2106028247 @default.
- W2911541619 cites W2107748267 @default.
- W2911541619 cites W2109733580 @default.
- W2911541619 cites W2110053085 @default.
- W2911541619 cites W2117934962 @default.
- W2911541619 cites W2118218470 @default.
- W2911541619 cites W2123564531 @default.
- W2911541619 cites W2129439365 @default.
- W2911541619 cites W2131329527 @default.
- W2911541619 cites W2143219656 @default.
- W2911541619 cites W2150047077 @default.
- W2911541619 cites W2150980522 @default.
- W2911541619 cites W2152640480 @default.
- W2911541619 cites W2154358910 @default.
- W2911541619 cites W2157912742 @default.
- W2911541619 cites W2165940852 @default.
- W2911541619 cites W2168828075 @default.
- W2911541619 cites W2168891225 @default.
- W2911541619 cites W2193407239 @default.
- W2911541619 cites W2207284635 @default.
- W2911541619 cites W2277631453 @default.
- W2911541619 cites W2289996588 @default.
- W2911541619 cites W2471799393 @default.
- W2911541619 cites W2539247695 @default.
- W2911541619 cites W2590102148 @default.
- W2911541619 cites W2604317749 @default.
- W2911541619 cites W2805204013 @default.
- W2911541619 cites W4231036548 @default.
- W2911541619 cites W4252184622 @default.
- W2911541619 doi "https://doi.org/10.1093/brain/awz002" @default.
- W2911541619 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30726881" @default.
- W2911541619 hasPublicationYear "2019" @default.
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