Department of Human Neurosciences, Sapienza University of Rome, 00185 Rome, Italy.
IRCCS Neuromed Institute, 86077 Pozzilli (IS), Italy.
Brain. 2023 Sep 1;146(9):3705-3718. doi: 10.1093/brain/awad114.
Although rigidity is a cardinal motor sign in patients with Parkinson's disease (PD), the instrumental measurement of this clinical phenomenon is largely lacking, and its pathophysiological underpinning remains still unclear. Further advances in the field would require innovative methodological approaches able to measure parkinsonian rigidity objectively, discriminate the different biomechanical sources of muscle tone (neural or visco-elastic components), and finally clarify the contribution to 'objective rigidity' exerted by neurophysiological responses, which have previously been associated with this clinical sign (i.e. the long-latency stretch-induced reflex). Twenty patients with PD (67.3 ± 6.9 years) and 25 age- and sex-matched controls (66.9 ± 7.4 years) were recruited. Rigidity was measured clinically and through a robotic device. Participants underwent robot-assisted wrist extensions at seven different angular velocities randomly applied, when ON therapy. For each value of angular velocity, several biomechanical (i.e. elastic, viscous and neural components) and neurophysiological measures (i.e. short and long-latency reflex and shortening reaction) were synchronously assessed and correlated with the clinical score of rigidity (i.e. Unified Parkinson's Disease Rating Scale-part III, subitems for the upper limb). The biomechanical investigation allowed us to measure 'objective rigidity' in PD and estimate the neuronal source of this phenomenon. In patients, 'objective rigidity' progressively increased along with the rise of angular velocities during robot-assisted wrist extensions. The neurophysiological examination disclosed increased long-latency reflexes, but not short-latency reflexes nor shortening reaction, in PD compared with control subjects. Long-latency reflexes progressively increased according to angular velocities only in patients with PD. Lastly, specific biomechanical and neurophysiological abnormalities correlated with the clinical score of rigidity. 'Objective rigidity' in PD correlates with velocity-dependent abnormal neuronal activity. The observations overall (i.e. the velocity-dependent feature of biomechanical and neurophysiological measures of objective rigidity) would point to a putative subcortical network responsible for 'objective rigidity' in PD, which requires further investigation.
虽然僵硬是帕金森病(PD)患者的主要运动征象,但这种临床现象的仪器测量在很大程度上仍然缺乏,其病理生理学基础仍不清楚。该领域的进一步进展需要创新的方法学方法,能够客观地测量帕金森氏僵硬,区分肌肉张力的不同生物力学来源(神经或粘弹性成分),并最终阐明以前与该临床体征相关的神经生理反应对“客观僵硬”的贡献(即长潜伏期拉伸诱导反射)。招募了 20 名 PD 患者(67.3±6.9 岁)和 25 名年龄和性别匹配的对照组(66.9±7.4 岁)。通过机器人设备进行临床和机器人测量来测量僵硬度。当患者接受治疗时,参与者以随机施加的七种不同角速度进行机器人辅助腕部伸展。对于每个角速度值,同时评估了几个生物力学(即弹性、粘性和神经成分)和神经生理测量(即短潜伏期和长潜伏期反射和缩短反应),并与僵硬的临床评分(即统一帕金森病评定量表第 III 部分,上肢分项)相关联。生物力学研究允许我们测量 PD 中的“客观僵硬”并估计这种现象的神经元来源。在患者中,在机器人辅助腕部伸展过程中,随着角速度的升高,“客观僵硬”逐渐增加。与对照组相比,神经生理学检查显示 PD 患者的长潜伏期反射增加,但短潜伏期反射和缩短反应没有增加。仅在 PD 患者中,长潜伏期反射随着角速度的增加而逐渐增加。最后,特定的生物力学和神经生理学异常与僵硬的临床评分相关。PD 中的“客观僵硬”与依赖于速度的异常神经元活动相关。总的观察结果(即生物力学和神经生理学客观僵硬测量的速度依赖性特征)表明,存在一个潜在的皮质下网络负责 PD 中的“客观僵硬”,这需要进一步研究。