William S. Middleton Memorial Veterans Hospital, Madison, WI 53792, USA.
Brain Imaging Behav. 2011 Sep;5(3):203-11. doi: 10.1007/s11682-011-9124-5.
Although [(18)F]fluoro-L: -dopa [FDOPA] positron emission tomography (PET) has been used as a surrogate outcome measure in Parkinson's disease therapeutic trials, this biomarker has not been proven to reflect clinical status longitudinally. We completed a retrospective analysis of relationships between computerized sampling of motor performance, FDOPA PET, and clinical outcome scales, repeated over 4 years, in 26 Parkinson's disease (PD) patients and 11 healthy controls. Mixed effects analyses showed that movement time and tongue strength best differentiated PD from control subjects. In the treated PD cohort, motor performance measures changed gradually in contrast to a steady decline in striatal FDOPA uptake. Prolonged reaction and movement time were related to lower caudate nucleus FDOPA uptake, and abnormalities in hand fine force control were related to mean striatal FDOPA uptake. These findings provide evidence that regional loss of nigrostriatal inputs to frontostriatal networks affects specific aspects of motor function.
尽管 [(18)F]氟-L-多巴 [FDOPA] 正电子发射断层扫描 (PET) 已被用作帕金森病治疗试验的替代结局指标,但该生物标志物尚未被证明能纵向反映临床状况。我们对 26 名帕金森病 (PD) 患者和 11 名健康对照者在 4 年内重复进行的运动表现、FDOPA PET 和临床结局量表的计算机采样之间的关系进行了回顾性分析。混合效应分析表明,运动时间和舌强最能区分 PD 患者和对照组。在治疗的 PD 队列中,运动表现指标逐渐变化,而纹状体 FDOPA 摄取则稳定下降。延长的反应时间和运动时间与尾状核 FDOPA 摄取减少有关,手部精细力量控制异常与纹状体 FDOPA 摄取的平均值有关。这些发现提供了证据,表明黑质纹状体传入到额纹状体网络的区域性丧失会影响运动功能的特定方面。