1 PET Centre, Department of Nuclear Medicine, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai 200040, China.
2 Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Brain. 2014 Dec;137(Pt 12):3122-8. doi: 10.1093/brain/awu290. Epub 2014 Oct 22.
Rapid eye movement sleep behaviour disorder has been evaluated using Parkinson's disease-related metabolic network. It is unknown whether this disorder is itself associated with a unique metabolic network. 18F-fluorodeoxyglucose positron emission tomography was performed in 21 patients (age 65.0±5.6 years) with idiopathic rapid eye movement sleep behaviour disorder and 21 age/gender-matched healthy control subjects (age 62.5±7.5 years) to identify a disease-related pattern and examine its evolution in 21 hemi-parkinsonian patients (age 62.6±5.0 years) and 16 moderate parkinsonian patients (age 56.9±12.2 years). We identified a rapid eye movement sleep behaviour disorder-related metabolic network characterized by increased activity in pons, thalamus, medial frontal and sensorimotor areas, hippocampus, supramarginal and inferior temporal gyri, and posterior cerebellum, with decreased activity in occipital and superior temporal regions. Compared to the healthy control subjects, network expressions were elevated (P<0.0001) in the patients with this disorder and in the parkinsonian cohorts but decreased with disease progression. Parkinson's disease-related network activity was also elevated (P<0.0001) in the patients with rapid eye movement sleep behaviour disorder but lower than in the hemi-parkinsonian cohort. Abnormal metabolic networks may provide markers of idiopathic rapid eye movement sleep behaviour disorder to identify those at higher risk to develop neurodegenerative parkinsonism.
快速眼动睡眠行为障碍已通过帕金森病相关代谢网络进行评估。尚不清楚这种障碍本身是否与独特的代谢网络有关。对 21 名特发性快速眼动睡眠行为障碍患者(年龄 65.0±5.6 岁)和 21 名年龄/性别匹配的健康对照者(年龄 62.5±7.5 岁)进行了 18F-氟脱氧葡萄糖正电子发射断层扫描,以确定疾病相关模式,并检查其在 21 名半帕金森病患者(年龄 62.6±5.0 岁)和 16 名中度帕金森病患者(年龄 56.9±12.2 岁)中的演变。我们确定了一个快速眼动睡眠行为障碍相关的代谢网络,其特征是桥脑、丘脑、内侧额区和感觉运动区、海马体、缘上回和颞下回以及小脑后叶活动增加,而枕叶和颞叶上区活动减少。与健康对照组相比,该障碍患者和帕金森病患者队列的网络表达升高(P<0.0001),但随着疾病的进展而降低。快速眼动睡眠行为障碍患者的帕金森病相关网络活动也升高(P<0.0001),但低于半帕金森病患者队列。异常代谢网络可能为特发性快速眼动睡眠行为障碍提供标志物,以识别那些更易发展为神经退行性帕金森病的患者。