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Motor patterns of patients with spinal muscular atrophy suggestive of sensory and corticospinal contributions to the development of locomotor muscle synergies.
Cheung, Vincent C K; Ha, Sophia C W; Zhang-Lea, Janet H; Chan, Zoe Y S; Teng, Yanling; Yeung, Geshi; Wu, Lingqian; Liang, Desheng; Cheung, Roy T H.
Afiliação
  • Cheung VCK; School of Biomedical Sciences, and Gerald Choa Neuroscience Institute, The Chinese University of Hong Kong, Hong Kong, China.
  • Ha SCW; Joint Laboratory of Bioresources and Molecular Research of Common Diseases, The Chinese University of Hong Kong and Kunming Institute of Zoology of the Chinese Academy of Sciences, Hong Kong, China.
  • Zhang-Lea JH; School of Biomedical Sciences, and Gerald Choa Neuroscience Institute, The Chinese University of Hong Kong, Hong Kong, China.
  • Chan ZYS; Department of Health and Physical Education, The Education University of Hong Kong, Hong Kong, China.
  • Teng Y; School of Nursing and Human Physiology, Gonzaga University, Spokane, Washington, United States.
  • Yeung G; Faculty of Kinesiology, University of Calgary, Calgary, Alberta, Canada.
  • Wu L; State Key Laboratory of Medical Genetics and School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Liang D; School of Biomedical Sciences, and Gerald Choa Neuroscience Institute, The Chinese University of Hong Kong, Hong Kong, China.
  • Cheung RTH; Department of Psychology, University of Pennsylvania, Philadelphia, Pennsylvania, United States.
J Neurophysiol ; 131(2): 338-359, 2024 Feb 01.
Article em En | MEDLINE | ID: mdl-38230872
ABSTRACT
Complex locomotor patterns are generated by combination of muscle synergies. How genetic processes, early sensorimotor experiences, and the developmental dynamics of neuronal circuits contribute to the expression of muscle synergies remains elusive. We shed light on the factors that influence development of muscle synergies by studying subjects with spinal muscular atrophy (SMA, types II/IIIa), a disorder associated with degeneration and deafferentation of motoneurons and possibly motor cortical and cerebellar abnormalities, from which the afflicted would have atypical sensorimotor histories around typical walking onset. Muscle synergies of children with SMA were identified from electromyographic signals recorded during active-assisted leg motions or walking, and compared with those of age-matched controls. We found that the earlier the SMA onset age, the more different the SMA synergies were from the normative. These alterations could not just be explained by the different degrees of uneven motoneuronal losses across muscles. The SMA-specific synergies had activations in muscles from multiple limb compartments, a finding reminiscent of the neonatal synergies of typically developing infants. Overall, while the synergies shared between SMA and control subjects may reflect components of a core modular infrastructure determined early in life, the SMA-specific synergies may be developmentally immature synergies that arise from inadequate activity-dependent interneuronal sculpting due to abnormal sensorimotor experience and other factors. Other mechanisms including SMA-induced intraspinal changes and altered cortical-spinal interactions may also contribute to synergy changes. Our interpretation highlights the roles of the sensory and descending systems to the typical and abnormal development of locomotor modules.NEW & NOTEWORTHY This is likely the first report of locomotor muscle synergies of children with spinal muscular atrophy (SMA), a subject group with atypical developmental sensorimotor experience. We found that the earlier the SMA onset age, the more the subjects' synergies deviated from those of age-matched controls. This result suggests contributions of the sensory/corticospinal activities to the typical expression of locomotor modules, and how their disruptions during a critical period of development may lead to abnormal motor modules.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Músculo Esquelético Tipo de estudo: Prognostic_studies Limite: Child / Humans / Infant / Newborn Idioma: En Revista: J Neurophysiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Músculo Esquelético Tipo de estudo: Prognostic_studies Limite: Child / Humans / Infant / Newborn Idioma: En Revista: J Neurophysiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China