HM CINAC (Centro Integral de Neurociencias Abarca Campal), Hospital Universitario HM Puerta del Sur, HM Hospitales, Madrid, Spain.
Universidad San Pablo-CEU, Madrid, Spain.
Brain. 2022 Apr 29;145(3):1018-1028. doi: 10.1093/brain/awab378.
The striatal dopaminergic deficit in Parkinson's disease exhibits a typical pattern, extending from the caudal and dorsal putamen at onset to its more rostral region as the disease progresses. Clinically, upper-limb onset of cardinal motor features is the rule. Thus, according to current understanding of striatal somatotopy (i.e. the lower limb is dorsal to the upper limb) the assumed pattern of early dorsal striatal dopaminergic denervation in Parkinson's disease does not fit with an upper-limb onset. We have examined the topography of putaminal denervation in a cohort of 23 recently diagnosed de novo Parkinson's disease patients and 19 age-/gender-matched healthy subjects assessed clinically and by 18F-DOPA PET; 15 patients were re-assessed after 2 years. There was a net upper-limb predominance of motor features at onset. Caudal denervation of the putamen was confirmed in both the more- and less-affected hemispheres and corresponding hemibodies. Spatial covariance analysis of the most affected hemisphere revealed a pattern of 18F-DOPA uptake rate deficit that suggested focal dopamine loss starting in the posterolateral and intermediate putamen. Functional MRI group-activation maps during a self-paced motor task were used to represent the somatotopy of the putamen and were then used to characterize the decline in 18F-DOPA uptake rate in the upper- and lower-limb territories. This showed a predominant decrement in both hemispheres, which correlated significantly with severity of bradykinesia. A more detailed spatial analysis revealed a dorsoventral linear gradient of 18F-DOPA uptake rate in Parkinson's disease patients, with the highest putamen denervation in the caudal intermediate subregion (dorsoventral plane) compared to healthy subjects. The latter area coincides with the functional representation of the upper limb. Clinical motor assessment at 2-year follow-up showed modest worsening of parkinsonism in the primarily affected side and more noticeable increases in the upper limb in the less-affected side. Concomitantly, 18F-DOPA uptake rate in the less-affected putamen mimicked that recognized on the most-affected side. Our findings suggest that early dopaminergic denervation in Parkinson's disease follows a somatotopically related pattern, starting with the upper-limb representation in the putamen and progressing over a 2-year period in the less-affected hemisphere. These changes correlate well with the clinical presentation and evolution of motor features. Recognition of a precise somatotopic onset of nigrostriatal denervation may help to better understand the onset and progression of dopaminergic neurodegeneration in Parkinson's disease and eventually monitor the impact of putative therapies.
帕金森病纹状体多巴胺能缺陷呈现出典型模式,从疾病发作时的壳核尾部和背侧延伸至更向前的区域。临床上,上肢起始的主要运动特征是常见的。因此,根据目前对纹状体躯体定位(即下肢位于上肢的背侧)的理解,帕金森病早期背侧纹状体多巴胺能神经支配的假设模式与上肢起始不符。我们检查了 23 名新诊断的帕金森病患者和 19 名年龄和性别匹配的健康对照者的壳核神经支配的分布情况,这些患者均接受了临床和 18F-DOPA PET 评估;其中 15 名患者在 2 年后进行了重新评估。在疾病发作时,上肢具有明显的运动特征优势。壳核的尾部在双侧和对应的半侧躯体中都有明显的神经支配缺失。对最受影响的半侧进行空间协方差分析显示,18F-DOPA 摄取率缺陷的模式表明多巴胺缺失起始于壳核的后外侧和中间部。在自我调节运动任务期间的功能磁共振组激活图用于表示壳核的躯体定位,然后用于描述 18F-DOPA 摄取率在上肢和下肢区域的下降。这表明在双侧半球都有明显的下降,与运动迟缓的严重程度显著相关。更详细的空间分析显示,帕金森病患者的 18F-DOPA 摄取率存在一个背腹向线性梯度,与健康对照者相比,壳核的中间尾部区域(背腹平面)的神经支配缺失最高。该区域与上肢的功能代表区域相吻合。在 2 年随访时的临床运动评估显示,主要受影响侧的帕金森病有适度恶化,而在受影响较小的侧上肢则有更明显的增加。同时,在受影响较小的壳核中,18F-DOPA 摄取率与在受影响较大的侧上观察到的摄取率相似。我们的发现表明,帕金森病的早期多巴胺能神经支配遵循一种与躯体定位相关的模式,从壳核的上肢代表区开始,在 2 年内进展到对侧半球。这些变化与运动特征的临床表现和演变很好地相关。对黑质纹状体神经支配的精确躯体定位起始的认识可能有助于更好地理解帕金森病多巴胺能神经退行性变的起始和进展,并最终监测潜在治疗方法的效果。