Prevalence and correlates of REM sleep behaviour disorder in patients with major depressive disorder: a two-phase study

重性抑郁障碍 医学 多导睡眠图 精神科 内科学 快速眼动睡眠行为障碍 萧条(经济学) 快速眼动睡眠 临床心理学 心情 脑电图 宏观经济学 经济
作者
Jing Wang,Steven Wai Ho Chau,Siu Ping Lam,Yaping Liu,Jihui Zhang,Ngan Yin Chan,Maxine Ming Sum Cheung,Mandy Wai Man Yu,Jessie CC. Tsang,Joey Wing Yan Chan,Bei Huang,Shirley Xin Li,Vincent Mok,Yun Kwok Wing
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:93 (9): 1010-1017 被引量:17
标识
DOI:10.1136/jnnp-2021-327460
摘要

To investigate the prevalence and clinical correlates of video polysomnography (vPSG)-confirmed rapid eye movement sleep behaviour disorder (RBD) in patients with major depressive disorder (MDD).This is a clinic-based two-phase epidemiological study. In phase 1, patients with MDD were screened by a validated questionnaire, RBD Questionnaire-Hong Kong (RBDQ-HK). In phase 2, a subsample of both the screen-positive (RBDQ-HK >20) and screen-negative patients with MDD underwent further clinical and sleep assessment (vPSG) to confirm the diagnosis of RBD (MDD+RBD). Poststratification weighting method was used to estimate the prevalence of MDD+RBD. The total likelihood ratio and the probability of prodromal Parkinson's disease (PD) were calculated from prodromal markers and risk factors, as per the Movement Disorder Society research criteria.A total of 455 patients with MDD were screened (median age (IQR)=52.66 (15.35) years, 77.58% woman, 43.74% positive). Eighty-one patients underwent vPSG and 12 of them were confirmed MDD+RBD. The prevalence of MDD+RBD was estimated to be 8.77% (95% CI: 4.33% to 16.93%), with possibly male predominance. MDD+RBD were associated with colour vision and olfaction deficit and a higher probability for prodromal PD.Almost 9% of patients with MDD in the psychiatric outpatient clinic has vPSG-confirmed RBD. Comorbid MDD+RBD may represent a subtype of MDD with underlying α-synucleinopathy neurodegeneration. Systematic screening of RBD symptoms and necessity of vPSG confirmation should be highlighted for capturing this MDD subtype with a view to enhance personalised treatment and future neuroprotection to prevent neurodegeneration.
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