Disease associations of excessive daytime sleepiness in multiple sclerosis: A prospective study.

Peter V Sguigna, Sabeen Toranian, Lauren M Tardo, Kyle M Blackburn, Lindsay A Horton, Darrel Conger, Ethan Meltzer, R Nick Hogan, Morgan C McCreary, Phyllis C Zee, Joseph S Takahashi, Benjamin M Greenberg
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引用次数: 1

Abstract

Background: Excessive daytime sleepiness (EDS) in multiple sclerosis (MS) can be a significant source of disability. Despite this, its prevalence as a patient-reported outcome in this condition has not been well established, and its causes are not well understood.

Methods: We prospectively assessed EDS as part of an observational study for patients referred for diagnostic neuro-ophthalmological testing. EDS was evaluated by the Epworth Sleepiness Scale (ESS), and visual data were also collected as part of a research protocol. Analysis with patient data was performed following the exclusion of patients with known primary sleep disorders.

Results: A total of 69 patients with MS were included in the analysis. The mean ESS was 6.5 with a SD of 4.3. ESS ≥ 10 was present in 23% of the cohort even in the presence of minimal mean neurological disability (Patient Determined Disease Steps (PDDS) = 1.5). The ESS score was not associated with age, sex, disease-related disability, retinal nerve fiber layer (RNFL), or optic neuritis (ON), but displayed an association with visual dysfunction.

Conclusions: There is an increased prevalence of EDS in MS. The increased values of the ESS are not explained by other sleep disorders, suggesting separate mechanisms. Further study of the underlying mechanisms is warranted.

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多发性硬化症患者日间过度嗜睡与疾病的关系:一项前瞻性研究。
背景:多发性硬化症(MS)患者白天过度嗜睡(EDS)可能是残疾的重要来源。尽管如此,在这种情况下,其作为患者报告的结果的患病率尚未得到很好的确定,其原因也未得到很好的理解。方法:我们前瞻性地评估EDS作为一项观察性研究的一部分,用于转诊进行诊断性神经眼科检查的患者。通过Epworth嗜睡量表(ESS)评估EDS,并收集视觉数据作为研究方案的一部分。在排除已知的原发性睡眠障碍患者后,对患者数据进行分析。结果:共有69例MS患者纳入分析。平均ESS为6.5,SD为4.3。即使存在最小的平均神经功能障碍,23%的队列也存在ESS≥10(患者确定疾病步骤(PDDS) = 1.5)。ESS评分与年龄、性别、疾病相关残疾、视网膜神经纤维层(RNFL)或视神经炎(ON)无关,但与视觉功能障碍有关。结论:多发性硬化症患者的EDS患病率增加,但其他睡眠障碍无法解释其升高的值,可能存在不同的机制。对潜在机制的进一步研究是必要的。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
期刊最新文献
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