Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Biomedical Research Institute, Busan, Republic of Korea.
Parkinsonism Relat Disord. 2022 Oct;103:42-49. doi: 10.1016/j.parkreldis.2022.08.006. Epub 2022 Aug 21.
Almost half of the nigral neurons are already lost during the preclinical period of Parkinson's disease (PD), and then the speed of neuronal loss is slowly attenuated during the subsequent progression. We sought to establish long-term temporal trajectory models for the dopaminergic input to the striatal subregions and a 4D-temporal trajectory model for the dopamine transporter positron emission tomography (PET).
We selected 83 patients in PD spectrum who underwent dopamine transporter PET scan twice and 71 age-matched healthy controls. We created temporal trajectories of specific binding ratios of the striatal subregions by integrating function between baseline values and their annual change rates and also created 4D-temporal trajectory model by applying the same method for each striatal voxel. Using the PET data of additional 100 PD patients, we estimated an individual time point in the 4D-temporal trajectory model for the validation.
Degenerative loss of striatal dopaminergic input first appeared in the posterior dorsal putamen in the more affected side at 14.4 years before the clinical onset, and subsequently in the posterior ventral and anterior putamen, and finally in the caudate. The time delay between the initiation of dopaminergic loss in the more and less affected posterior dorsal putamen was 6.1 years. The estimated individual time points within the entire disease course were correlated with the motor severity.
Our temporal trajectory model demonstrated a sequential loss of dopaminergic input in the striatal subregions in PD and may be beneficial for the evaluation of individual status of disease progression.
在帕金森病(PD)的临床前阶段,几乎已有一半的黑质神经元丢失,随后神经元丢失的速度在随后的进展中缓慢减弱。我们试图建立纹状体亚区多巴胺能传入的长期时间轨迹模型和多巴胺转运蛋白正电子发射断层扫描(PET)的 4D 时间轨迹模型。
我们选择了 83 名处于 PD 谱中的患者,这些患者进行了两次多巴胺转运蛋白 PET 扫描,还有 71 名年龄匹配的健康对照者。我们通过整合基线值与其年变化率之间的功能,为纹状体亚区的特定结合比创建了时间轨迹,还通过对每个纹状体体素应用相同的方法创建了 4D 时间轨迹模型。利用另外 100 名 PD 患者的 PET 数据,我们在 4D 时间轨迹模型中对每个个体的时间点进行了估计,以验证。
纹状体多巴胺能传入的退行性丧失首先出现在临床发病前 14.4 年的更受影响侧的后背侧壳核中,随后出现在后腹侧和前壳核,最后出现在尾状核。更受影响和较不受影响的后背侧壳核中多巴胺能丧失的起始时间间隔为 6.1 年。整个疾病过程中个体时间点的估计与运动严重程度相关。
我们的时间轨迹模型显示了 PD 患者纹状体亚区多巴胺能传入的顺序丧失,这可能有助于评估个体疾病进展状况。