Istituto di Neurologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Brain. 2010 Sep;133(9):2664-76. doi: 10.1093/brain/awq221.
Deep brain stimulation of the subthalamic nucleus represents the most important innovation for treatment of advanced Parkinson's disease. Prospective studies have shown that although the beneficial effects of this procedure are maintained at 5 years, axial motor features and cognitive decline may occur in the long term after the implants. In order to address some unsolved questions raised by previous studies, we evaluated a series of 20 consecutive patients who received continuous stimulation for 8 years. The overall motor improvement reported at 5 years (55.5% at Unified Parkinson's Disease Rating Scale-motor part, P < 0.001 compared with baseline) was only partly retained 3 years later (39%, P < 0.001, compared with baseline; -16.5%, P < 0.01, compared with 5 years), with differential effects on motor features: speech did not improve and postural stability worsened (P < 0.05). The preoperative levodopa equivalent daily dose was reduced by 58.2% at 5 years and by 60.3% at 8 years. In spite of subtle worsening of motor features, a dramatic impairment in functional state (-56.6% at Unified Parkinson's Disease Rating Scale-Activities of Daily Living, P < 0.01) emerged after the fifth year of stimulation. The present study did not reveal a predictive value of preoperative levodopa response, whereas few single features at baseline (such as gait and postural stability motor scores and the preoperative levodopa equivalent daily dose) could predict long-term motor outcome. A decline in verbal fluency (slightly more pronounced than after 5 years) was detected after 8 years. A significant but slight decline in tasks of abstract reasoning, episodic memory and executive function was also found. One patient had developed dementia at 5 years with further progression at 8 years. Executive dysfunction correlated significantly with postural stability, suggesting interplay between axial motor deterioration and cognition. Eight years after surgery, no significant change was observed on scales assessing depression or anxiety when compared with baseline. At 8 years, there was no significant increase of side-effects when compared with 5-year follow-up. In conclusion, deep brain stimulation of the subthalamic nucleus is a safe procedure with regard to cognitive and behavioural morbidity over long-term follow-up. However, the global benefit partly decreases later in the course of the disease, due to progression of Parkinson's disease and the appearance of medication- and stimulation-resistant symptoms.
丘脑底核深部脑刺激是治疗晚期帕金森病最重要的创新手段。前瞻性研究表明,尽管该手术的有益效果在 5 年内保持不变,但在植入物后长期,轴向运动特征和认知下降可能会发生。为了解决之前研究提出的一些未解决的问题,我们评估了连续 20 例接受 8 年连续刺激的患者。在 5 年时报告的整体运动改善(统一帕金森病评定量表运动部分的 55.5%,与基线相比,P < 0.001)仅在 3 年后部分保留(39%,P < 0.001,与基线相比;-16.5%,P < 0.01,与 5 年相比),对运动特征有不同的影响:言语无改善,姿势稳定性恶化(P < 0.05)。术前左旋多巴等效日剂量在 5 年时减少了 58.2%,在 8 年时减少了 60.3%。尽管运动特征略有恶化,但在刺激后的第五年出现了功能状态的急剧恶化(统一帕金森病评定量表日常生活活动评分降低 56.6%,P < 0.01)。本研究未发现术前左旋多巴反应的预测价值,而少数基线时的单一特征(如步态和姿势稳定性运动评分以及术前左旋多巴等效日剂量)可预测长期运动结果。8 年后发现言语流畅性下降(比 5 年后稍明显)。还发现抽象推理、情景记忆和执行功能的任务也有显著但轻微的下降。一名患者在 5 岁时出现痴呆,8 岁时进一步进展。执行功能与姿势稳定性显著相关,提示轴向运动恶化与认知之间的相互作用。与基线相比,术后 8 年时评估抑郁或焦虑的量表无明显变化。与 5 年随访相比,8 年后副作用无明显增加。总之,丘脑底核深部脑刺激在长期随访中与认知和行为发病率有关,是一种安全的手术。然而,由于帕金森病的进展和出现药物和刺激抵抗症状,整体益处在疾病后期会部分减少。