PROJECT SUMMARY/ABSTRACT
Cerebral palsy (CP) results from a perinatal brain injury and is one of the most prevalent and costly pediatric
neurologic conditions in the United States. Individuals with CP frequently experience lifelong mobility challenges.
The modern treatment approaches being used to overcome these challenges place greater emphasis on the
neurological basis for how youth with CP plan their leg movements, execute motor actions, and integrate sensory
information. Despite this neuroscience-informed approach, these new therapies are still limited by substantial
knowledge gaps regarding how the aberrant sensorimotor cortical activity and/or spinal cord specifically affects
the gait of youth with CP.
Our ultramodern magnetoencephalographic (MEG) brain imaging results have revealed that cortical aberrations
play a substantial role in the uncharacteristic leg motor actions and sensory processes seen in youth with CP.
Furthermore, our high-resolution MRI pipelines have shown that the structural integrity of spinal cord tissue is
compromised in individuals with CP. From these experiments, we have inferred that the altered cortical dynamics
and spinal cord integrity likely impacts the ability of youth with CP to make feed-forward predictions and/or online
corrections to their leg kinematics during gait. However, this conjecture has yet to be fully established due to
physical limitations of the MEG/MRI recording environments. To move forward, we will use our extensive MEG
foundational work to develop new electroencephalographic (EEG) methods that have the scientific rigor and
flexibility to precisely quantify the sensorimotor cortical activity during real-time gait. Furthermore, we will utilize
cutting-edge neurophysiological tests to concurrently quantify how the spinal cord interneuronal dynamics are
modulated during gait. The Aims of this study will: (1) establish multimodal MEG-EEG neuroimaging proxies of
the aberrant sensorimotor cortical oscillations seen in youth with CP that are known to impact the extent of the
mobility deficits, (2) quantify the sensorimotor EEG cortical oscillations and spinal cord interneuronal dynamics
of youth with CP during gait, and (3) decipher if alterations in the sensorimotor cortical oscillations and spinal
cord interneuronal dynamics are better predictors of the mobility deficits seen in youth with CP relative to the
most commonly used clinical metrics. To achieve these Aims, youth with CP and neurotypical controls will
undergo a series of experiments that will use simultaneous MEG-EEG neuroimaging, EEG neuroimaging during
gait, and assessments of the spinal cord interneuronal dynamics during gait. Furthermore, the participants will
undergo a battery of clinical assessments (e.g., balance, spasticity, selective control, strength and sensation).
We foresee that the body of new knowledge gained through this project will set-the-stage for the design and
testing of innovative therapeutic protocols that target the specific neurophysiological deficits that are limiting the
mobility of youth with CP.