Long‐Term Globus Pallidus Internus Deep Brain Stimulation in Pediatric Non‐Degenerative Dystonia: A Cohort Study and a Meta‐Analysis

Author:

Duga Valentina12ORCID,Giossi Riccardo34ORCID,Romito Luigi Michele5ORCID,Stanziano Mario6,Levi Vincenzo7,Panteghini Celeste8,Zorzi Giovanna1ORCID,Nardocci Nardo1

Affiliation:

1. Child Neuropsychiatry Unit, Department of Pediatric Neuroscience Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

2. Child and Adolescent Neuropsychiatric Unit, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano Italy

3. Poison Control Center and Clinical Pharmacology Unit ASST Grande Ospedale Metropolitano Niguarda Milano Italy

4. Department of Research and Clinical Development, Scientific Directorate Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

5. Movement Disorders Unit, Neurology Department Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

6. Neuroradiology Unit, Department of Technology and Diagnosis Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

7. Functional Neurosurgery Unit, Neurosurgery Department Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

8. Molecular Neurogenetics Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milano Italy

Abstract

AbstractBackgroundThe evidence in the effectiveness of deep brain stimulation in children with medication‐refractory non‐degenerative monogenic dystonia is heterogeneous and long‐term results are sparse.ObjectivesThe objective is to describe long‐term outcomes in a single‐center cohort and compare our results with a meta‐analysis cohort form literature.MethodsWe performed a retrospective single‐center cohort study including consecutive pediatric patients with non‐degenerative genetic or idiopathic dystonia treated with globus pallidus internus deep brain stimulation at our center and a systematic review and individual‐patient data meta‐analysis with the same inclusion criteria. The primary outcome was the change from baseline in the Burke‐Fahn‐Marsden Dystonia Rating Scale‐movement (BFMDRS‐M) score.ResultsThe clinical cohort included 25 patients with a mean study follow‐up of 11.4 years. The meta‐analysis cohort included 224 patients with a mean follow‐up of 3 years. Overall, the BFMDRS‐M mean improvements at 1 year and at last follow‐up were 41% and 33% in the clinical cohort and 58.9% and 57.2% in the meta‐analysis cohort, respectively. TOR1A‐dystonia showed the greatest and most stable BFMDRS‐M improvement in both cohorts at 1 year and at last follow‐up (76.3% and 74.3% in the clinical cohort; 69.6% and 67.3% in the meta‐analysis cohort), followed by SGCE‐dystonia (63% and 63.9% in the meta‐analysis cohort). THAP1‐dystonia (70.1% and 29.8% in the clinical cohort; 52.3% and 42.0% in the meta‐analysis cohort) and KMT2B‐dystonia (33.3% and 41.3% in the clinical cohort; 38.0% and 26.7% in the meta‐analysis cohort) showed a less pronounced or sustained response.ConclusionGlobus pallidus deep brain stimulation long‐term treatment seems effective with a possible gene‐specific differential effect. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Ministero della Salute

Publisher

Wiley

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