Asanuma Kotaro, Tang Chengke, Ma Yilong, Dhawan Vijay, Mattis Paul, Edwards Christine, Kaplitt Michael G, Feigin Andrew, Eidelberg David
Center for Neurosciences, Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, Manhasset, NY 11030, USA.
Brain. 2006 Oct;129(Pt 10):2667-78. doi: 10.1093/brain/awl162. Epub 2006 Jul 14.
It has been proposed that deep brain stimulation (DBS) of the subthalamic nucleus (STN DBS) and dopaminergic therapy ameliorate the symptoms of Parkinson's disease through similar functional mechanisms. We examined this notion using PET to compare the metabolic effects of these treatment approaches. Nine Parkinson's disease patients (age 61.7 +/- 11.1 years) were scanned ON and OFF STN stimulation and nine others (age 60.0 +/- 9.3 years) were scanned ON and OFF an individual titrated intravenous levodopa infusion. The two treatment groups were matched for baseline disease severity as well as clinical response to therapy. Similarities and differences in the effects of treatment on regional metabolism were assessed using statistical parametric mapping (SPM). In addition, we used network analysis to assess the effect of therapy on the expression of an abnormal Parkinson's disease-related spatial covariance pattern (PDRP). We found that both STN DBS and levodopa therapy were associated with significant (P < 0.001) metabolic reductions in the putamen/globus pallidus, sensorimotor cortex and cerebellar vermis, as well as increases in the precuneus (BA 7). The metabolic effects of the two interventions differed in the STN and medial prefrontal cortex, with relative increases with stimulation in the former structure and decreases in the latter. Network quantification disclosed reductions in PDRP activity with both interventions, which correlated with clinical improvement (P < 0.05). The degree of network modulation by therapy did not differ significantly for the two treatment approaches (P > 0.6). These findings support the results of previous imaging studies indicating that effective symptomatic therapies for Parkinson's disease involve a common mechanism. The modulation of pathological brain networks is a critical feature of the treatment response in parkinsonism.
有人提出,丘脑底核深部脑刺激(STN DBS)和多巴胺能疗法通过相似的功能机制改善帕金森病症状。我们使用正电子发射断层扫描(PET)来比较这些治疗方法的代谢效应,以检验这一观点。对9名帕金森病患者(年龄61.7±11.1岁)在丘脑底核刺激开启和关闭时进行扫描,另外9名患者(年龄60.0±9.3岁)在个体化滴定静脉左旋多巴输注开启和关闭时进行扫描。两个治疗组在基线疾病严重程度以及对治疗的临床反应方面进行了匹配。使用统计参数映射(SPM)评估治疗对区域代谢影响的异同。此外,我们使用网络分析来评估治疗对异常帕金森病相关空间协方差模式(PDRP)表达的影响。我们发现,STN DBS和左旋多巴治疗均与壳核/苍白球、感觉运动皮层和小脑蚓部的显著(P<0.001)代谢降低以及楔前叶(BA 7)的代谢增加有关。两种干预措施在丘脑底核和内侧前额叶皮层的代谢效应有所不同,前者结构中刺激后相对增加,后者则减少。网络量化显示两种干预措施均使PDRP活性降低,且与临床改善相关(P<0.05)。两种治疗方法对网络的调节程度无显著差异(P>0.6)。这些发现支持了先前影像学研究的结果,表明帕金森病有效的对症治疗涉及共同机制。病理性脑网络的调节是帕金森病治疗反应的关键特征。