Kilbane Camilla, Witt Jennifer, Galifianakis Nicholas B, Glass Graham A, Volz Monica, Heath Susan, Starr Philip A, Ostrem Jill Louise
University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
Swedish Medical Center Neuroscience Institute, Seattle, Washington, USA.
Stereotact Funct Neurosurg. 2018;96(5):320-326. doi: 10.1159/000492823. Epub 2018 Nov 27.
X-linked dystonia parkinsonism (XDP) causes adult-onset progressive dystonia and parkinsonism, which may not respond to pharmacotherapy.
Previous case reports have reported beneficial effects from bilateral pallidal (GPi) deep brain stimulation (DBS). Here, we report the long-term clinical outcomes of 3 patients treated at our center.
All patients presented with medication refractory dystonia and parkinsonism. They were followed prospectively. Clinical evaluations included the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) and the Unified Parkinson's Disease Rating Scale (UPDRS). Adverse events were recorded.
The average length of follow-up was 45.7 months. No serious adverse events occurred. All patients experienced an immediate and sustained improvement in dystonia. Mean percentage improvement in motor subscores of BFMDRS was 63.5% at the last follow-up visit. Parkinsonism was less responsive to neuromodulation, with a mean improvement in UPDRS-III of 39.5%. Standard pallidal stimulation parameters were used. Freezing of gait developed after DBS therapy in 2 patients, stimulation-induced in one and due to disease progression in the other.
Bilateral pallidal DBS resulted in significant and sustained improvement in dystonia and moderate improvement in parkinsonism. Pallidal DBS represents an important treatment option for XPD for the management of motor symptoms.
X连锁肌张力障碍帕金森综合征(XDP)导致成人起病的进行性肌张力障碍和帕金森综合征,药物治疗可能无效。
既往病例报告显示双侧苍白球内侧部(GPi)脑深部电刺激(DBS)有有益效果。在此,我们报告在我们中心接受治疗的3例患者的长期临床结果。
所有患者均表现为药物难治性肌张力障碍和帕金森综合征。对他们进行前瞻性随访。临床评估包括伯克-法恩-马尔登肌张力障碍评定量表(BFMDRS)和统一帕金森病评定量表(UPDRS)。记录不良事件。
平均随访时间为45.7个月。未发生严重不良事件。所有患者的肌张力障碍均立即且持续改善。在最后一次随访时,BFMDRS运动亚评分的平均改善百分比为63.5%。帕金森综合征对神经调节的反应较差,UPDRS-III的平均改善率为39.5%。使用了标准的苍白球刺激参数。2例患者在DBS治疗后出现步态冻结,其中1例由刺激诱发,另1例由疾病进展导致。
双侧苍白球DBS使肌张力障碍得到显著且持续的改善,帕金森综合征得到中度改善。苍白球DBS是XDP运动症状管理的重要治疗选择。