Correlations with REM sleep behavior disorder severity in isolated rapid eye movement sleep behavior disorders patients

被引:3
|
作者
Kim, Sang Jin [1 ,2 ]
Chung, Eun Ju [1 ,2 ]
Ji, Ki-Hwan [1 ]
Kang, Mi-Ri [1 ]
Hong, Jin Yong [3 ]
Lee, Sunseong [4 ]
Park, Ji Sun [4 ]
Oh, Jungsu S. [5 ]
Kim, Jae Seung [5 ]
Kang, Suk Yun [6 ]
机构
[1] Inje Univ, Coll Med, Busan Paik Hosp, Dept Neurol, Busan, South Korea
[2] Inje Univ, Dementia & Neurodegenerat Dis Res Ctr, Busan, South Korea
[3] Yonsei Univ, Wonju Coll Med, Dept Neurol, Wonju, Gangwon Do, South Korea
[4] Inje Univ, Coll Med, Busan Paik Hosp, Dept Nucl Med, Busan, South Korea
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
[6] Hallym Univ, Coll Med, Dongtan Sacred Heart Hosp, Dept Neurol, 7,Keunjaebong Gil, Hwaseong 18450, Gyeonggi Do, South Korea
关键词
Isolated rapid eye movement sleep behavior disorders; alpha-synucleinopathy; neurodegeneration; gait; PET; pain; visuospatial; NEURODEGENERATION; DIAGNOSIS; DISEASE;
D O I
10.1080/00207454.2021.2019034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objectives The pathogenesis of isolated rapid eye movement sleep behavior disorders (iRBD) is poorly understood. The severity of RBD may reflect its pathogenesis. Methods We compared motor function and non-motor symptoms (NMSs) between iRBD patients and healthy volunteers. We correlated motor function, NMSs, and striatal dopaminergic activity with RBD severity using video-polysomnography. Results Twenty-one iRBD patients and 17 controls participated. The Unified Parkinson's Disease Rating Scale part III scores were higher in patients compared to controls (p < 0.001). There was no difference in upper extremity function between patients and controls (right, p = 0.220; left, p = 0.209), but gait was slower in iRBD patients (walking time, p < 0.001; number of steps, p < 0.001). The mean value of the Korean version of the Mini-Mental State Exam and Clinical Dementia Rating were lower in patients (p = 0.006, p = 0.003, respectively). Patients with were also more depressed (p = 0.002), had decreased olfactory function (p < 0.001), reported more frequent sleep/fatigue episodes (p < 0.001), worse attention/memory capacity (p < 0.001), gastrointestinal problems (p = 0.009), urinary problems (p = 0.007), and pain (p = 0.083). Further, iRBD patients reported more frequent sleep-related disturbances (p = 0.004), but no difference in daytime sleepiness (p = 0.663). Disease severity was correlated with pain (r = 0.686, p = 0.002) and visuospatial function (r= -0.507, p = 0.038). There were no correlations between RBD severity and striatal dopaminergic activities (p > 0.09). Conclusions iRBD is a multisystem neurodegenerative disorder, and gait abnormalities may be a disease characteristic, possibly related to the akinetic-rigid phenotype of Parkinson's disease. The correlation between pain/visuospatial dysfunction and RBD severity may be related to its pathogenesis.
引用
收藏
页码:918 / 924
页数:7
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