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日间过度嗜睡预示特发性快速眼动睡眠行为障碍中的神经退行性变。

Excessive Daytime Sleepiness Predicts Neurodegeneration in Idiopathic REM Sleep Behavior Disorder.

作者信息

Zhou Junying, Zhang Jihui, Lam Siu Ping, Chan Joey Wy, Mok Vincent, Chan Anne, Li Shirley Xin, Liu Yaping, Tang Xiangdong, Yung Wing Ho, Wing Yun Kwok

机构信息

Department of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong SAR.

Sleep Medicine Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Sleep. 2017 May 1;40(5). doi: 10.1093/sleep/zsx041.

Abstract

STUDY OBJECTIVES

To determine the association of excessive daytime sleepiness (EDS) with the conversion of neurodegenerative diseases in patients with idiopathic REM sleep behavior disorder (iRBD).

METHODS

A total of 179 patients with iRBD (79.1% males, mean age = 66.3 ± 9.8 years) were consecutively recruited. Forty-five patients with Epworth Sleepiness Scale score ≥14 were defined as having EDS. Demographic, clinical, and polysomnographic data were compared between iRBD patients with and without EDS. The risk of developing neurodegenerative diseases was examined using Cox proportional hazards model.

RESULTS

After a mean follow-up of 5.8 years (SD = 4.3 years), 50 (27.9%) patients developed neurodegenerative diseases. There was a significantly higher proportion of conversion in patients with EDS compared to those without EDS (42.2 % vs. 23.1%, p = .01). EDS significantly predicted an increased risk of developing neurodegenerative diseases (adjusted hazard ratios [HR] = 2.56, 95% confidence interval [CI] 1.37 to 4.77) after adjusting for age, sex, body mass index, current depression, obstructive sleep apnea, and periodic limb movements during sleep. Further analyses demonstrated that EDS predicted the conversion of Parkinson's disease (PD) (adjusted HR = 3.55, 95% CI 1.59 to 7.89) but not dementia (adjusted HR = 1.48, 95% CI 0.44 to 4.97).

CONCLUSIONS

EDS is associated with an increased risk of developing neurodegenerative diseases, especially PD, in patients with iRBD. Our findings suggest that EDS is a potential clinical biomarker of α-synucleinopathies in iRBD.

摘要

研究目的

确定特发性快速眼动睡眠行为障碍(iRBD)患者日间过度嗜睡(EDS)与神经退行性疾病转化之间的关联。

方法

连续招募了179例iRBD患者(男性占79.1%,平均年龄 = 66.3 ± 9.8岁)。45例Epworth嗜睡量表评分≥14分的患者被定义为患有EDS。对有和没有EDS的iRBD患者的人口统计学、临床和多导睡眠图数据进行了比较。使用Cox比例风险模型检查发生神经退行性疾病的风险。

结果

平均随访5.8年(标准差 = 4.3年)后,50例(27.9%)患者发生了神经退行性疾病。与没有EDS的患者相比,有EDS的患者转化率显著更高(42.2%对23.1%,p = 0.01)。在调整年龄、性别、体重指数、当前抑郁、阻塞性睡眠呼吸暂停和睡眠期间周期性肢体运动后,EDS显著预测了发生神经退行性疾病的风险增加(调整后的风险比[HR] = 2.56,95%置信区间[CI] 1.37至4.77)。进一步分析表明,EDS预测了帕金森病(PD)的转化(调整后的HR = 3.55,95% CI 1.59至7.89),但未预测痴呆(调整后的HR = 1.48,95% CI 0.44至4.97)。

结论

在iRBD患者中,EDS与发生神经退行性疾病尤其是PD的风险增加有关。我们的研究结果表明,EDS是iRBD中α-突触核蛋白病的潜在临床生物标志物。

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