Investigation of autonomic function in idiopathic REM sleep behavior disorder

被引:49
作者
Frauscher, Birgit [1 ]
Nomura, Takashi [2 ]
Duerr, Susanne [1 ]
Ehrmann, Laura [1 ]
Gschliesser, Viola [1 ]
Wenning, Gregor K. [1 ]
Wolf, Elisabeth [1 ]
Inoue, Yuichi [3 ]
Hoegl, Birgit [1 ]
Poewe, Werner [1 ]
机构
[1] Innsbruck Med Univ, Dept Neurol, A-6020 Innsbruck, Austria
[2] Tottori Univ, Fac Med, Div Neurol, Dept Brain & Neurosci, Yonago, Tottori 683, Japan
[3] Japan Somnol Ctr, Neuropsychiat Res Inst, Tokyo, Japan
关键词
Risk marker; REM sleep behavior disorder; COMPASS; Neurodegenerative disease; Autonomic function; NEURODEGENERATIVE DISEASE; OLFACTORY DYSFUNCTION; EARLY MARKER; BRAIN-STEM; IMPAIRMENT;
D O I
10.1007/s00415-011-6298-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Idiopathic REM sleep behavior disorder (iRBD) has been suggested as an early "pre-motor" stage of Parkinson's disease (PD) in a significant proportion of cases. We investigated autonomic function in 15 consecutive iRBD patients and compared these findings to PD patients and healthy controls. All participants underwent cardiovascular autonomic function testing, and were rated on the COMPASS scale. Symptomatic orthostatic hypotension was present in two iRBD patients, two PD patients and none of the healthy controls. In the tilt table examination, blood pressure changes were similar between iRBD patients and healthy controls. In the PD group, blood pressure drops were more pronounced. In the orthostatic standing test, iRBD patients had higher blood pressure changes than healthy controls. Highest drops were found in PD. Valsalva ratio was lower in iRBD and PD compared to healthy controls. Total COMPASS score was higher in iRBD compared to healthy controls. Highest scores were found in PD. These results support the presence of autonomic dysfunction in iRBD. On several measures, dysfunction was intermediate between healthy controls and PD consistent with the concept that iRBD can be manifestation of synuclein-associated neurodegenerative disorders. Follow-up studies are needed to determine whether iRBD patients with dysfunction on several autonomic domains are at particular risk for developing one of these diseases.
引用
收藏
页码:1056 / 1061
页数:6
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