Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Neurotoxicology. 2018 Jan;64:43-49. doi: 10.1016/j.neuro.2017.07.004. Epub 2017 Jul 8.
Occupational manganese (Mn) exposure is associated with the development of parkinsonism; however, the mechanism of neurotoxicity is unknown. Brain positron emission tomography (PET) imaging provides a non-invasive method of assessing dopamineric neuronal function. 6-[F]fluoro-L-DOPA (FDOPA) PET reflects in-vivo nigrostriatal function, but results in Mn exposure are conflicting. The objective of this study was to investigate the association between Mn exposure secondary to occupational welding, FDOPA striatal uptake, and clinical parkinsonism as measured by Unified Parkinson Disease Rating Scale motor subscore 3 (UPDRS3) scores. FDOPA PET scans were acquired on 72 subjects (27 Mn-exposed welders, 14 other Mn-exposed workers, and 31 non-exposed subjects). We estimated cumulative welding exposure from detailed work histories, and a movement disorders specialist examined all subjects. Striatal volumes of interest were identified on aligned magnetic resonance imaging (MRI) for each subject. Specific striatal FDOPA uptake was calculated with a graphical analysis method. We used linear regression while adjusting for age to assess the association between welding exposure and FDOPA uptake in the caudate, anterior putamen, and posterior putamen. Compared to the non-exposed subjects, mean caudate FDOPA uptake was 0.0014min (95% confidence interval [CI] 0.0008, 0.0020) lower in Mn-exposed welders and 0.0012min (95% CI 0.0005, 0.0019) lower in other Mn-exposed workers (both p≤0.001). There was no clear dose-response association between caudate FDOPA uptake and Mn exposure or UPDRS3 scores. Mn-exposed welders and workers demonstrated lower caudate FDOPA uptake, indicating pre-synaptic dopaminergic dysfunction in Mn-exposed subjects that was not associated with clinical parkinsonism.
职业性锰(Mn)暴露与帕金森病的发生有关;然而,其神经毒性机制尚不清楚。脑正电子发射断层扫描(PET)成像提供了一种评估多巴胺能神经元功能的非侵入性方法。6-[F]氟-L-多巴(FDOPA)PET 反映了体内黑质纹状体功能,但 Mn 暴露的结果存在矛盾。本研究的目的是调查由于职业焊接导致的 Mn 暴露与 FDOPA 纹状体摄取以及使用统一帕金森病评定量表运动评分 3(UPDRS3)测量的临床帕金森病之间的关系。对 72 名受试者(27 名 Mn 暴露焊工、14 名其他 Mn 暴露工人和 31 名非暴露受试者)进行了 FDOPA PET 扫描。我们根据详细的工作史估计了累积焊接暴露量,运动障碍专家对所有受试者进行了检查。为每位受试者的磁共振成像(MRI)对齐的纹状体识别感兴趣区。使用图形分析方法计算特定纹状体 FDOPA 摄取。我们使用线性回归,同时调整年龄,以评估焊接暴露与尾状核、前壳核和后壳核中 FDOPA 摄取之间的关系。与非暴露受试者相比,Mn 暴露焊工的尾状核 FDOPA 摄取平均低 0.0014min(95%置信区间 [CI] 0.0008,0.0020),其他 Mn 暴露工人低 0.0012min(95% CI 0.0005,0.0019)(均 P≤0.001)。尾状核 FDOPA 摄取与 Mn 暴露或 UPDRS3 评分之间没有明显的剂量反应关系。Mn 暴露焊工和工人表现出较低的尾状核 FDOPA 摄取,表明 Mn 暴露受试者存在突触前多巴胺能功能障碍,但与临床帕金森病无关。