周期性肢体运动障碍患者运动皮质脑灌注改变

E. Joo, Jung Sik Kim, S. Hong
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通信地址:Seung Bong Hong, MD,博士,韩国首尔江南区irwon洞50号成均馆大学医学院三星医疗中心神经内科电话:+82-2-3410-3592传真:+82-2-3410-0052 E-mail: ejoo@skku.edu eyuns@paran.com目的:睡眠相关运动疾病的病理生理学和运动障碍中的睡眠功能障碍尚未被广泛了解。脑功能成像,特别是放射性同位素技术,被认为是研究周期性肢体运动障碍(PLMD)病理机制的有力工具。方法:对25例未用药的PLMD患者和23例年龄和性别匹配的正常人在清醒状态下进行tc -半胱氨酸乙酯二聚体脑单光子发射计算机断层扫描。为了进行统计参数映射分析,将单光子发射计算机断层扫描图像在空间上归一化为标准模板,然后在高斯核半最大值处使用14mm全宽度进行平滑。结果:患者平均年龄48.6岁,男性占一半以上。大多数患者报告因反复腿跳引起的睡眠发作和持续失眠。失眠的平均持续时间为7.5年。他们否认有不宁腿综合症的病史,也没有睡眠障碍,如阻塞性睡眠呼吸暂停综合症,这些都是由多导睡眠图证实的。睡眠时平均PLM指数和运动唤醒指数分别显著提高至45.3和7.5/hr。他们的睡眠质量比正常患者差。在PLMD患者中,与正常对照相比,双侧中央前回的脑血流量显著增加。患者未见脑区灌注减少。局部脑灌注与任何多导睡眠图参数(包括PLMS指数或运动唤醒指数)均无相关性。结论:双侧初级运动皮质不同的灌注模式可能是PLMD患者运动皮质损伤的证据。[J]睡眠研究,2011;8:35-39
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered Cerebral Perfusion of Motor Cortex in Patients with Periodic Limb Movement Disorder
Address for correspondence Seung Bong Hong, MD, PhD Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, Seoul 135-710, Korea Tel: +82-2-3410-3592 Fax: +82-2-3410-0052 E-mail: ejoo@skku.edu eyuns@paran.com Objectives: The pathophysiology of sleep-related motor diseases and sleep dysfunction in movement disorders is widely unknown as yet. Functional brain imaging, in particular radioisotope techniques, is considered to be powerful tool to investigate pathomechanisms of periodic limb movement disorder (PLMD). Methods: We performed Tc-ethyl cysteinate dimer brain single-photon emission computed tomography in 25 drug-naive patients with PLMD and 23 age-and gender matched normal cotrols during wakefulness. For statistical parametric mapping analysis, single-photon emission computed tomography images were spatially normalized to the standard template and then smoothed using a 14-mm full width at half maximum Gaussian kernel. Results: Mean age of patients and normal controls was 48.6 years and over half of them were male. Most patients reported the sleep onset and maintenance insomnia due to repetitive leg jerks. Average duration of insomnia was 7.5 years. They denied the history of restless leg syndrome and there was no sleep disorders such as obstructive sleep apnea syndrome which was confirmed by polysomnography. Mean PLM during sleep index and movement arousal index were markedly increased to 45.3/hr and 7.5/hr, respectively. Their sleep quality was poorer than that of normal patients. In PLMD patients, cerebral blood flow was significantly increased in the bilateral precentral gyri as compared to normal controls. There was no brain region showing decreased perfusion in patients. Regional cerebral perfusion was not correlated to any polysomnography parameter including PLMS index or movement arousal index. Conclusions: Different perfusion pattern in bilateral primary motor cortices may provide the evidences of motor cortical impairment in patients with PLMD. J Korean Sleep Res Soc 2011;8:35-39
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