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Published on: August 12, 2018
Cerebellar deep brain stimulation for the treatment of movement disorders in cerebral palsy
Iahn Cajigas1, Melanie A Morrison2, Marta San Luciano3
1Departments of1Neurological Surgery.
Insights
Deep brain stimulation (DBS) targeting the cerebellum shows promise for treating dyskinetic cerebral palsy (DCP). This safe, preliminary study in three patients demonstrated significant improvements in motor function and subjective symptoms.
Area of Science:
- Neurology
- Neurosurgery
- Biomedical Engineering
Background:
- Cerebral palsy (CP) is the most common childhood physical disability, affecting movement and posture due to early brain damage.
- Dyskinetic cerebral palsy (DCP) involves dystonia and choreoathetosis, often with basal ganglia damage unsuitable for standard deep brain stimulation (DBS) targets.
- The cerebellum, frequently spared in hypoxic-ischemic encephalopathy, presents a potential alternative target for DCP treatment.
Purpose of the Study:
- To evaluate the safety and preliminary efficacy of bilateral cerebellar deep brain stimulation (DBS) targeting the dentate nucleus (DN) in patients with DCP.
- To explore the feasibility of chronic neural recording and neuromodulation in the cerebellar dentate nucleus for DCP.
Main Methods:
- Three patients with DCP underwent bilateral cerebellar DBS implantation, targeting the dentate nucleus and cerebellar outflow pathways.
- Continuous deep brain stimulation (DBS) was delivered using a pulse generator capable of sensing local field potentials.
- Surgical methods, chronic cerebellar recordings, and preliminary clinical outcomes using the Burke-Fahn-Marsden Dystonia Rating Scale were reported.
Main Results:
- All three patients tolerated the cerebellar DBS procedure well, with no reported complications.
- Patients exhibited subjective improvements in motor function, including hand movements, coordination, gait, and speech.
- Objective improvements were noted in the Burke-Fahn-Marsden Dystonia Rating Scale movement subscale, with a 19%-40% response range.
Conclusions:
- Deep brain stimulation (DBS) of the dentate nuclei appears to be a safe therapeutic option for patients with DCP.
- Preliminary clinical benefits suggest that cerebellar DBS may alleviate motor symptoms in DCP.
- Further research with larger cohorts and long-term follow-up is necessary to confirm the efficacy and understand the mechanisms of cerebellar neuromodulation in DCP.
Objective:
Cerebral palsy (CP) represents the most common childhood physical disability that encompasses disorders of movement and posture attributed to nonprogressive disturbances that occurred in the developmental fetal or infant brain. Dyskinetic CP (DCP), the second most common type of CP after spastic forms, refers to a subset of patients in whom dystonia and choreoathetosis are the predominant motor manifestations. Most children with CP have abnormal brain MRI studies indicative of cortical and deep gray matter damage consistent with hypoxic ischemic encephalopathy, which may preclude or suggest decreased efficacy of standard deep brain stimulation (DBS) targets. The cerebellum has been posited as an attractive target for treatment of DCP because it is frequently spared from hypoxic ischemic damage and has shown promise in alleviating patient symptoms both in early work in the 1970s and in more recent case series with DBS.
Methods:
The authors performed bilateral cerebellar DBS implantation, targeting the dentate nucleus (DN) and cerebellar outflow pathway, in 3 patients with DCP. Leads were connected to a pulse generator that senses local field potentials during chronic continuous DBS. The authors report their surgical methods, examples of chronic cerebellar local field potential recordings, and preliminary clinical outcomes. Motor outcomes were assessed using the Burke-Fahn-Marsden Dystonia Rating Scale.
Results:
Three patients 14-22 years old with DCP and MRI evidence of structural damage to the basal ganglia were offered cerebellar stimulation targeting the DN. All patients tolerated the procedure well and demonstrated improvement in subjective motor function as well as objective improvement in the Burke-Fahn-Marsden Dystonia Rating Scale movement subscale, although the range of responses was variable (19%-40%). Patients experienced subjective improvement in motor function including ease of hand movements and coordination, gait, head control, speech, decreased overflow, and diminished muscle tightness.
Conclusions:
DBS of the dentate nuclei in patients with DCP appears to be safe and shows preliminary evidence of clinical benefit. New chronic sensing technology may allow for determination of in vivo mechanisms of network disruption in DCP and allow for further understanding of the effects of neuromodulation on brain physiology. Larger studies with long-term follow up will be required to further elucidate the clinical benefits of this therapy. This report addresses a gap in the literature regarding the technical approach to image-based stereotactic targeting and chronic neural recording in the DN.

