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Clinical Features and Correlates of Poor Nighttime Sleepiness in Patients with Parkinson’s Disease

机译:帕金森病患者夜间嗜睡性差的临床特征及相关性

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摘要

Objective. The present study investigated the clinical features and correlates of poor nighttime sleepiness (PNS) in patients with Parkinson’s disease (PD). Methods. One hundred ten patients with PD (divided into PD-PNS group and PD-nPNS group) and forty-seven controls (nPD-PNS group) were enrolled in this study. Demographic information was collected. Patients were assessed according to the unified Parkinson’s disease rating scale (UPDRS) and Hoehn–Yahr (H&Y) stage scale. Patients were also evaluated according to the Pittsburgh sleep quality index (PSQI), Epworth sleepiness scale (ESS), rapid eye movement sleep behavior disorder screening questionnaire (RBD-SQ), restless leg syndrome (RLS) diagnosis, Hamilton’s depression scale (HAMD), and Hamilton’s anxiety scale (HAMA). Results. The prevalence of PNS was 55.45% (61/110) in patients with PD. The PD-PNS group tended to have a longer duration of disease, higher UPDRS-I and UPDRS-III scores, a higher percentage of RLS patients, and higher HAMA and HAMD scores than those of the PD-nPNS group. The PD-PNS group tended to have a higher percentage of RBD and RLS patients and higher HAMA and HAMD scores than those of the nPD-PNS group. Analysis of the PSQI components and PSQI impact factors showed that the PD-PNS group had worse subjective sleep quality (χ2 = −2.267, P = 0.023), shorter sleep latency (χ2 = −2.262, P = 0.024), fewer sleep medications (χ2 = −4.170, P ≤ 0.001), worse daytime functioning (χ2 = −2.347, P = 0.019), and an even higher prevalence of increased nocturia (χ2 = 4.447, P = 0.035), nightmares (χ2 = 7.887, P = 0.005), and pain (χ2 = 9.604, P = 0.002) than those of the nPD-PNS group. Analysis also indicated that the PSQI global score positively correlated with BMI (r = 0.216, P < 0.05), H&Y stage (r = 0.223, P < 0.05), UPDRS-I (r = 0.501, P < 0.01), UPDRS-III (r = 0.425, P < 0.01), ESS (r = −0.296, P < 0.01), RBD (r = 0.227, P < 0.05), RLS (r = 0.254, P < 0.01), HAMA (r = 0.329, P < 0.01), and HAMD (r = 0.466, P < 0.01). In the final model, H&Y stage, RLS, UPDRS-III, and HAMD remained associated with the PQSI score (P ≤ 0.001, P ≤ 0.001, P = 0.049, P ≤ 0.001, respectively). Conclusions. Our data showed that PNS was common in patients with PD. H&Y stage, UPDRS-III, HAMD, and RLS were positively associated with PNS. Attention to the management of motor symptoms, RLS, and depression may be beneficial to nighttime sleep quality in patients with PD.
机译:客观的。本研究调查的临床特点及患者的帕金森病(PD)差夜间嗜睡(PNS)的相关因素。方法。一百一十名PD患者(分为PD-PNS组和PD-NPN晶体管组)和47控件(NPD-PNS组)的研究对象。人口信息收集。根据统一帕金森病评定量表(UPDRS)和霍恩-Yahr分级(H&Y)级规模的患者进行了评估。患者根据匹兹堡睡眠质量指数(PSQI),Epworth嗜睡量表(ESS),快速眼动睡眠行为障碍筛查问卷(RBD-SQ),不宁腿综合征(RLS)的诊断,汉密尔顿抑郁量表(HAMD)也评价和汉密尔顿焦虑量表(HAMA)。结果。 PNS的患病率是PD患者55.45%(61/110)。该PD-PNS组往往有疾病的病程长,较高的UPDRS-I和UPDRS-Ⅲ评分,RLS患者的比例较高,而较高的HAMA和HAMD评分均较PD-NPN晶体管组。该PD-PNS组往往有RBD和RLS患者的比例较高和较高的HAMA和HAMD评分均较NPD-PNS组。的PSQI组件和PSQI影响因素的分析表明,PD-PNS组具有更差主观睡眠质量(χ2= -2.267,P = 0.023),更短的睡眠潜伏期(χ2= -2.262,P = 0.024),更少的睡眠药物( χ2= -4.170,P≤0.001),更糟糕的日间功能(χ2= -2.347,P = 0.019),并增加夜尿(χ2= 4.447的甚至发病率较高,P = 0.035),恶梦(χ2= 7.887,P = 0.005),和疼痛(χ2= 9.604,P = 0.002)比那些NPD-PNS组。分析还表明,PSQI全局得分与BMI(R = 0.216,P <0.05),H&Y工作台(R = 0.223,P <0.05),UPDRS-I(R = 0.501,P <0.01),UPDRS-III正相关(R = 0.425,P <0.01),ESS(R = -0.296,P <0.01),RBD(R = 0.227,P <0.05),RLS(R = 0.254,P <0.01),HAMA(R = 0.329, P <0.01),和HAMD(R = 0.466,P <0.01)。在最终模型中,H&Y阶段,RLS,UPDRS-III,和HAMD保持与PQSI分数(P≤0.001,P≤0.001,P = 0.049,P≤0.001)相关联。结论。我们的数据显示,PNS PD患者很常见。 H&Y台,UPDRS-III,HAMD和RLS均与PNS有关。注意运动症状,RLS,和抑郁症的管理可能是PD患者夜间睡眠质量有益。

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