Ipsilesional trajectory control is related to contralesional arm paralysis after left hemisphere damage

Kathleen Y. Haaland, Sydney Y. Schaefer, Robert T. Knight, John Adair, Alvaro Magalhaes, Joseph Sadek, Robert L. Sainburg

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

45 Citas (Scopus)

Resumen

We have recently shown ipsilateral dynamic deficits in trajectory control are present in left hemisphere damaged (LHD) patients with paresis, as evidenced by impaired modulation of torque amplitude as response amplitude increases. The purpose of the current study is to determine if these ipsilateral deficits are more common with contralateral hemiparesis and greater damage to the motor system, as evidenced by structural imaging. Three groups of right-handed subjects (healthy controls, LHD stroke patients with and without upper extremity paresis) performed single-joint elbow movements of varying amplitudes with their left arm in the left hemispace. Only the paretic group demonstrated dynamic deficits characterized by decreased modulation of peak torque (reflected by peak acceleration changes) as response amplitude increased. These results could not be attributed to lesion volume or peak velocity as neither variable differed across the groups. However, the paretic group had damage to a larger number of areas within the motor system than the non-paretic group suggesting that such damage increases the probability of ipsilesional deficits in dynamic control for modulating torque amplitude after left hemisphere damage.

Idioma originalEnglish
Páginas (desde-hasta)195-204
Número de páginas10
PublicaciónExperimental Brain Research
Volumen196
N.º2
DOI
EstadoPublished - jun. 2009
Publicado de forma externa

Nota bibliográfica

Funding Information:
Acknowledgments This research was supported by a Department of Veterans AVairs Medical Merit Review and Rehabilitation Merit Review (B4476), the National Institutes of Health, National Institute for Child Health and Human Development (#RO1HD39311), National Institute on Aging training grant, Interdisciplinary Training in Gerontology (#T32AG00048). We gratefully acknowledge (1) Venkat Mannam for lesion analysis, (2) Jennifer Hogan, Rena Singleton, Lee Stapp, and Jennifer Rinehart for data collection, and (3) Dr. Sally Harris, HealthSouth Rehabilitation Hospital, Lovelace Medical Center, and Lovelace Rehabilitation Hospital for patient referral.

ASJC Scopus Subject Areas

  • General Neuroscience

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