Cross-sectional and longitudinal associations between probable rapid eye movement sleep behavior disorder and impulse control disorders in Parkinson's disease

被引:8
作者
Cao, R. [1 ,2 ,3 ]
Chen, X. [1 ,2 ,3 ]
Xing, F. [1 ,2 ,3 ]
Xie, C. [1 ,2 ,3 ]
Hu, P. [1 ,2 ,3 ]
Wang, K. [1 ,2 ,3 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Neurol, Hefei 230022, Anhui, Peoples R China
[2] Collaborat Innovat Ctr Neuropsychiat Disorder & M, Hefei, Anhui, Peoples R China
[3] Anhui Prov Key Lab Cognit & Neuropsychiat Disorde, Hefei, Anhui, Peoples R China
关键词
drug-naive; impulse control disorders; Parkinson's disease; prospective; RBD; REM sleep behavior disorder; PROGRESSION; SYMPTOMS; MARKER;
D O I
10.1111/ene.14177
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose The aim was to investigate whether probable rapid eye movement sleep behavior disorder (pRBD) is associated with impulse control disorders (ICDs) in drug-naive patients with Parkinson's disease (PD) and whether baseline pRBD is associated with a higher incidence of ICDs during follow-up. Methods The Parkinson's Progression Markers Initiative is an international, multicenter, prospective cohort study to identify biomarkers of PD progression. In all, 423 drug-naive patients with early-stage PD were included in the cross-sectional analysis, and 320 patients who screened negative for any ICDs or related behaviors at baseline were included in the longitudinal analysis. Results In the cross-sectional analysis, a significant correlation was found between pRBD and ICDs in drug-naive patients whilst controlling for potential confounders [odds ratio 2.56, 95% confidence interval (CI) 1.38-4.76, P = 0.003]. In the longitudinal analysis, baseline pRBD was an independent predictor of ICD development over time [hazard ratio (HR) 1.648, 95% CI 1.054-2.576; P = 0.028]. Other significant predictors of ICDs included younger age of onset (HR = 0.973, 95% CI = 0.950-0.997; P = 0.026) and greater State-Trait Anxiety Inventory score (HR = 1.040, 95% CI = 1.020-1.061; P < 0.001). Conclusion Our data suggest that identifying baseline pRBD in early-stage PD may help clinicians to choose a better therapeutic strategy so as to prevent or limit neuropsychiatric complications.
引用
收藏
页码:757 / 763
页数:7
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