Klinik und Poliklinik für Neurologie, Uniklinik Köln, Kerpener Str. 62, 50924 Köln, Germany.
Brain. 2010 Mar;133(Pt 3):701-12. doi: 10.1093/brain/awq022. Epub 2010 Mar 5.
Neurodegeneration with brain iron accumulation encompasses a heterogeneous group of rare neurodegenerative disorders that are characterized by iron accumulation in the brain. Severe generalized dystonia is frequently a prominent symptom and can be very disabling, causing gait impairment, difficulty with speech and swallowing, pain and respiratory distress. Several case reports and one case series have been published concerning therapeutic outcome of pallidal deep brain stimulation in dystonia caused by neurodegeneration with brain iron degeneration, reporting mostly favourable outcomes. However, with case studies, there may be a reporting bias towards favourable outcome. Thus, we undertook this multi-centre retrospective study to gather worldwide experiences with bilateral pallidal deep brain stimulation in patients with neurodegeneration with brain iron accumulation. A total of 16 centres contributed 23 patients with confirmed neurodegeneration with brain iron accumulation and bilateral pallidal deep brain stimulation. Patient details including gender, age at onset, age at operation, genetic status, magnetic resonance imaging status, history and clinical findings were requested. Data on severity of dystonia (Burke Fahn Marsden Dystonia Rating Scale-Motor Scale, Barry Albright Dystonia Scale), disability (Burke Fahn Marsden Dystonia Rating Scale-Disability Scale), quality of life (subjective global rating from 1 to 10 obtained retrospectively from patient and caregiver) as well as data on supportive therapy, concurrent pharmacotherapy, stimulation settings, adverse events and side effects were collected. Data were collected once preoperatively and at 2-6 and 9-15 months postoperatively. The primary outcome measure was change in severity of dystonia. The mean improvement in severity of dystonia was 28.5% at 2-6 months and 25.7% at 9-15 months. At 9-15 months postoperatively, 66.7% of patients showed an improvement of 20% or more in severity of dystonia, and 31.3% showed an improvement of 20% or more in disability. Global quality of life ratings showed a median improvement of 83.3% at 9-15 months. Severity of dystonia preoperatively and disease duration predicted improvement in severity of dystonia at 2-6 months; this failed to reach significance at 9-15 months. The study confirms that dystonia in neurodegeneration with brain iron accumulation improves with bilateral pallidal deep brain stimulation, although this improvement is not as great as the benefit reported in patients with primary generalized dystonias or some other secondary dystonias. The patients with more severe dystonia seem to benefit more. A well-controlled, multi-centre prospective study is necessary to enable evidence-based therapeutic decisions and better predict therapeutic outcomes.
脑铁沉积性神经退行性变包括一组罕见的神经退行性疾病,其特征是脑内铁沉积。严重的全身性肌张力障碍常常是一个突出的症状,并且非常致残,导致步态障碍、言语和吞咽困难、疼痛和呼吸困难。已经发表了几例关于脑铁变性神经退行性变引起的肌张力障碍的苍白球深部脑刺激治疗结果的病例报告和一个病例系列,报告结果大多是有利的。然而,由于病例研究,可能存在对有利结果的报告偏倚。因此,我们进行了这项多中心回顾性研究,以收集全球范围内脑铁沉积性神经退行性变患者双侧苍白球深部脑刺激的经验。共有 16 个中心贡献了 23 例经证实的脑铁沉积性神经退行性变和双侧苍白球深部脑刺激患者。要求提供患者详细信息,包括性别、发病年龄、手术年龄、遗传状况、磁共振成像状况、病史和临床发现。收集了关于肌张力障碍严重程度(Burke Fahn Marsden Dystonia Rating Scale-Motor Scale、Barry Albright Dystonia Scale)、残疾程度(Burke Fahn Marsden Dystonia Rating Scale-Disability Scale)、生活质量(主观全球评分,从患者和照顾者那里回顾性获得 1 到 10 分)以及支持性治疗、并发药物治疗、刺激设置、不良事件和副作用的数据。数据在术前、术后 2-6 个月和 9-15 个月采集一次。主要结局测量是肌张力障碍严重程度的变化。在 2-6 个月时,肌张力障碍严重程度的平均改善为 28.5%,在 9-15 个月时为 25.7%。术后 9-15 个月时,66.7%的患者肌张力障碍严重程度改善 20%或以上,31.3%的患者残疾程度改善 20%或以上。全球生活质量评分在 9-15 个月时中位数改善 83.3%。术前肌张力障碍严重程度和疾病持续时间预测术后 2-6 个月时肌张力障碍严重程度的改善;但在 9-15 个月时未达到统计学意义。该研究证实,脑铁沉积性神经退行性变患者的肌张力障碍可通过双侧苍白球深部脑刺激改善,尽管这种改善不如原发性全身性肌张力障碍或其他一些继发性肌张力障碍患者报告的那样大。病情较重的患者似乎受益更多。需要进行一项精心设计的、多中心的前瞻性研究,以便做出基于证据的治疗决策,并更好地预测治疗结果。