Huang Xiao-Jun, Wang Shi-Ge, Guo Xia-Nan, Tian Wo-Tu, Zhan Fei-Xia, Zhu Ze-Yu, Yin Xiao-Meng, Liu Qing, Yin Kai-Li, Liu Xiao-Rong, Zhang Yu, Liu Zhen-Guo, Liu Xiao-Li, Zheng Lan, Wang Tian, Wu Li, Rong Tian-Yi, Wang Yan, Zhang Mei, Bi Guang-Hui, Tang Wei-Guo, Zhang Chao, Zhong Ping, Wang Chun-Yu, Tang Jian-Guang, Lu Wei, Zhang Ru-Xu, Zhao Guo-Hua, Li Xun-Hua, Li Hua, Chen Tao, Li Hai-Yan, Luo Xiao-Guang, Song Yan-Yan, Tang Hui-Dong, Luan Xing-Hua, Zhou Hai-Yan, Tang Bei-Sha, Chen Sheng-Di, Cao Li
Department of Neurology, Rui Jin Hospital and Rui Jin Hospital North, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
China Paroxysmal Dyskinesia Collaborative Group (CPDCG), Shanghai, China.
Mov Disord. 2020 Aug;35(8):1428-1437. doi: 10.1002/mds.28061. Epub 2020 May 11.
Paroxysmal kinesigenic dyskinesia is a spectrum of involuntary dyskinetic disorders with high clinical and genetic heterogeneity. Mutations in proline-rich transmembrane protein 2 have been identified as the major pathogenic factor.
We analyzed 600 paroxysmal kinesigenic dyskinesia patients nationwide who were identified by the China Paroxysmal Dyskinesia Collaborative Group to summarize the clinical phenotypes and genetic features of paroxysmal kinesigenic dyskinesia in China and to provide new thoughts on diagnosis and therapy.
The China Paroxysmal Dyskinesia Collaborative Group was composed of departments of neurology from 22 hospitals. Clinical manifestations and proline-rich transmembrane protein 2 screening results were recorded using unified paroxysmal kinesigenic dyskinesia registration forms. Genotype-phenotype correlation analyses were conducted in patients with and without proline-rich transmembrane protein 2 mutations. High-knee exercises were applied in partial patients as a new diagnostic test to induce attacks.
Kinesigenic triggers, male predilection, dystonic attacks, aura, complicated forms of paroxysmal kinesigenic dyskinesia, clustering in patients with family history, and dramatic responses to antiepileptic treatment were the prominent features in this multicenter study. Clinical analysis showed that proline-rich transmembrane protein 2 mutation carriers were prone to present at a younger age and have longer attack duration, bilateral limb involvement, choreic attacks, a complicated form of paroxysmal kinesigenic dyskinesia, family history, and more forms of dyskinesia. The new high-knee-exercise test efficiently induced attacks and could assist in diagnosis.
We propose recommendations regarding diagnostic criteria for paroxysmal kinesigenic dyskinesia based on this large clinical study of paroxysmal kinesigenic dyskinesia. The findings offered some new insights into the diagnosis and treatment of paroxysmal kinesigenic dyskinesia and might help in building standardized paroxysmal kinesigenic dyskinesia clinical evaluations and therapies. © 2020 International Parkinson and Movement Disorder Society.
发作性运动诱发性运动障碍是一类非自主性运动障碍谱,具有高度的临床和遗传异质性。富含脯氨酸的跨膜蛋白2突变已被确定为主要致病因素。
我们分析了全国600例由中国发作性运动障碍协作组确诊的发作性运动诱发性运动障碍患者,以总结中国发作性运动诱发性运动障碍的临床表型和遗传特征,并为诊断和治疗提供新思路。
中国发作性运动障碍协作组由22家医院的神经内科组成。使用统一的发作性运动诱发性运动障碍登记表记录临床表现和富含脯氨酸的跨膜蛋白2筛查结果。对有和没有富含脯氨酸的跨膜蛋白2突变的患者进行基因型-表型相关性分析。对部分患者进行高抬腿运动作为一种新的诊断试验以诱发发作。
运动诱发性触发因素、男性易患、肌张力障碍发作、先兆、发作性运动诱发性运动障碍的复杂形式、家族史患者聚集以及对抗癫痫治疗的显著反应是这项多中心研究的突出特征。临床分析表明,富含脯氨酸的跨膜蛋白2突变携带者发病年龄倾向于较小,发作持续时间较长,双侧肢体受累,舞蹈样发作,发作性运动诱发性运动障碍的复杂形式,家族史以及更多形式的运动障碍。新的高抬腿运动试验能有效诱发发作并有助于诊断。
基于这项关于发作性运动诱发性运动障碍的大型临床研究,我们提出了关于发作性运动诱发性运动障碍诊断标准的建议。这些发现为发作性运动诱发性运动障碍的诊断和治疗提供了一些新见解,并可能有助于建立标准化的发作性运动诱发性运动障碍临床评估和治疗方法。© 2020国际帕金森病和运动障碍协会