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Tonic Electromyogram Density in Multiple System Atrophy with Predominant Parkinsonism and Parkinson's Disease

机译:帕金森病和帕金森病为主的多系统萎缩患者的强直性肌电图密度

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摘要

Background:Both Parkinson's disease (PD) and multiple system atrophy (MSA) have associated sleep disorders related to the underlying neurodegenerative pathology.Clinically,MSA with predominant parkinsonism (MSA-P) resembles PD in the manifestation of prominent parkinsonism.Whether the amount of rapid eye movement (REM) sleep without atonia could be a potential marker for differentiating MSA-P from PD has not been thoroughly investigated.This study aimed to examine whether sleep parameters could provide a method for differentiating MSA-P from PD.Methods:This study comprised 24 MSA-P patients and 30 PD patients,and they were of similar age,gender,and REM sleep behavior disorder (RBD) prevalence.All patients underwent clinical evaluation and one night of video-polysomnography recording.The tonic and phasic chin electromyogram (EMG) activity was manually quantified during REM sleep of each patient.We divided both groups in terms of whether they had RBD to make subgroup analysis.Results:No significant difference between MSA-P group and PD group had been found in clinical characteristics and sleep architecture.However,MSA-P patients had higher apnea-hypopnea index (AHI;1.15 [0.00,8.73]/h vs.0.00 [0.00,0.55]/h,P =0.024) and higher tonic chin EMG density (34.02 [18.48,57.18]% vs.8.40 [3.11,13.06]%,P < 0.001) as compared to PD patients.Subgroup analysis found that tonic EMG density in MSA + RBD subgroup was higher than that in PD + RBD subgroup (55.04 [26.81,69.62]% vs.11.40 [8.51,20.41]%,P < 0.001).Furthermore,no evidence of any difference in tonic EMG density emerged between PD + RBD and MSA-RBD subgroups (P > 0.05).Both disease duration (P =0.056) and AHI (P =0.051) showed no significant differences during subgroup analysis although there was a trend toward longer disease duration in PD + RBD subgroup and higher AHI in MSA-RBD subgroup.Stepwise multiple linear regression analysis identified the presence ofMSA-P (β =0.552,P < 0.001) and RBD (β =0.433,P < 0.001) as predictors of higher tonic EMG density.Conclusion:Tonic chin EMG density could be a potential marker for differentiating MSA-P from PD.
机译:背景:帕金森氏病(PD)和多系统萎缩症(MSA)均与潜在的神经退行性病理相关,与睡眠障碍相关。快速的眼动(REM)睡眠无心律失常可能是区分MSA-P和PD的潜在标志物。本研究旨在检查睡眠参数是否可以提供区分MSA-P和PD的方法。这项研究包括24名MSA-P患者和30名PD患者,他们的年龄,性别和REM睡眠行为障碍(RBD)患病率相似。所有患者均接受了临床评估,并进行了一夜的视频多导睡眠图记录。在每位患者的REM睡眠期间手动定量肌电图(EMG)活性。我们根据两组是否有RBD进行亚组分析。 MSA-P组和PD组之间在临床特征和睡眠结构上有显着差异。但是,MSA-P组的呼吸暂停低通气指数较高(AHI; 1.15 [0.00,8.73] / h vs.0.00 [0.00,0.55] ] / h,P = 0.024)和PD患者相比,下巴肌电图密度较高(34.02 [18.48,57.18]%vs.8.40 [3.11,13.06]%,P <0.001)。亚组分析发现, MSA + RBD分组高于PD + RBD分组(55.04 [26.81,69.62]%vs.11.40 [8.51,20.41]%,P <0.001)。此外,PD之间的肌电图肌密度没有任何差异的证据。 + RBD和MSA-RBD亚组(P> 0.05)。虽然PD + RBD亚组的疾病持续时间有延长的趋势,但亚组分析中疾病持续时间(P = 0.056)和AHI(P = 0.051)均无显着差异。逐步多元线性回归分析确定MSA-P(β= 0.552,P <0.001)和RBD(β= 0.433,P <0.001)的存在是预测因素结论:补剂下巴肌电图密度可能是区分MSA-P和PD的潜在标志。

著录项

  • 来源
    《中华医学杂志(英文版)》 |2017年第6期|684-690|共7页
  • 作者单位

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Institute of Neuroscience, Soochow University, Suzhou, Jiangsu 215123, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Institute of Neuroscience, Soochow University, Suzhou, Jiangsu 215123, China;

    Department of Neurology and Sleep Center, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

    Suzhou Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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