Novel utilization of deep brain stimulation in the pedunculopontine nucleus with globus pallidus internus for treatment of childhood-onset dystonia

被引:2
作者
MacLean, Jennifer A. [1 ,2 ]
Nataraj, Jaya [3 ]
Davies, Jordan [4 ,5 ]
Zakharova, Aleksandra [1 ,6 ]
Kurtz, Joshua [7 ]
Liker, Mark A. [4 ,8 ]
Olaya, Joffre [4 ,5 ]
Sanger, Terence D. [1 ,2 ,3 ,9 ]
机构
[1] Childrens Hosp Orange Cty, Dept Neurol, Orange, CA 92868 USA
[2] Childrens Hosp Orange Cty, Res Inst, Orange, CA 92868 USA
[3] Univ Calif Irvine, Samueli Sch Engn, Irvine, CA 92617 USA
[4] Childrens Hosp Orange Cty, Div Neurosurg, Orange, CA USA
[5] Univ Calif Irvine, Sch Med, Dept Neurol Surg, Irvine, CA USA
[6] Univ Desarrollo, Unit Pediat Neurol, Clin Alemana Santiago, Fac Med, Santiago, Chile
[7] Univ Calif Irvine, Sch Med, Irvine, CA USA
[8] Univ Southern Calif, Keck Sch Med, Dept Neurol Surg, Los Angeles, CA USA
[9] Univ Calif Irvine, Sch Med, Dept Pediat, Irvine, CA 92617 USA
来源
FRONTIERS IN HUMAN NEUROSCIENCE | 2023年 / 17卷
关键词
dystonia; pediatrics; pedunculopontine nucleus; deep brain stimulation; orofacial dyskinesia; stereotaxy; PARKINSONS-DISEASE; RELIABILITY; IMPROVES;
D O I
10.3389/fnhum.2023.1270430
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
IntroductionDeep brain stimulation (DBS) is a well-documented therapy for dystonia utilized in many adult and pediatric movement disorders. Pedunculopontine nucleus (PPN) has been investigated as a DBS target primarily in adult patients with dystonia or dyskinesias from Parkinson's disease, showing improvement in postural instability and gait dysfunction. Due to the difficulty in targeting PPN using standard techniques, it is not commonly chosen as a target for adult or pediatric pathology. There is no current literature describing the targeting of PPN in DBS for childhood-onset dystonia.MethodsTwo pediatric and one young adult patient with childhood-onset dystonia who underwent DBS implantation at our institution were identified. Patient 1 has Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration (MEPAN) syndrome. Patient 2 has Glutaric Aciduria Type 1 (GA1). Patient 3 has atypical pantothenate kinase-associated neurodegeneration (PKAN). PPN was identified as a potential target for these patients due to axial or orofacial dystonia. Pre- and post-operative videos taken as part of routine clinical assessments were evaluated and scored on the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) and Barry-Albright Dystonia Scale (BADS). All patients had permanent electrodes placed bilaterally in PPN and globus pallidus internus (GPi). A Likert scale on quality of life was also obtained from the patient/parents as applicable.ResultsSignificant programming was necessary over the first 3-12 months to optimize patients' response to stimulation. All patients experienced at least a 34% improvement in the BFMDRS score. Patients 2 and 3 also experienced an over 30% improvement in BADS score. All patients/parents appreciated improvement in quality of life postoperatively.DiscussionDeep brain stimulation in PPN was safely and successfully used in two pediatric patients and one young adult patient with childhood-onset dystonia. These patients showed clinically significant improvements in BFMDRS scoring post operatively. This represents the first reported DBS targeting of PPN in pediatric patients, and suggests that PPN is a possible target for pediatric-onset dystonia with axial and orofacial symptoms that may be refractory to traditional pallidal stimulation alone.
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