探索帕金森病患者正压性低血压与白天嗜睡之间的相互关系

Abhimanyu Mahajan, Kevin R Duque, Alok Kumar Dwivedi, Jesus Abanto, Luca Marsili, Emily J Hill, Ameya Saraf, Kelsey J McDonald, Adebukunola Arowosegbe, Heba A Deraz, Aaron Bloemer, Alberto J Espay
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摘要

导言:约50%的帕金森病(PD)患者会出现白天嗜睡的症状,这与帕金森病的高发病率、低生活质量和事故风险增加有关。虽然有报道称早期帕金森病患者的自主神经功能障碍与白天嗜睡之间存在关联,但我们对药物、认知状态和病程对这种关系的作用还缺乏足够的了解。方法对前瞻性辛辛那提队列生物标志物项目的数据进行分析。主要研究结果是白天嗜睡,由埃普沃斯嗜睡量表(ESS)测量。主要暴露变量是正张性低血压(OH),并对神经源性低血压(nOH)亚型进行了子分析。回归分析对以下协变量进行了调整:年龄、性别、病程、教育程度、合并症、抗胆碱能负担、左旋多巴当量剂量(LEDD)、运动障碍社会统一帕金森病评分量表的运动子评分、Hoehn和Yahr分期(H&Y)、贝克抑郁量表和贝克焦虑量表。结果 分析了 456 名帕金森病患者的数据。在对所有协变量进行调整后,OH与ESS评分密切相关,尤其是在使用抗胆碱能药物的受试者中(RC,4.30;p<0.001)。这种调整后的关联在病程早、H&Y分期早、无认知功能下降和LEDD≤750毫克的男性中更为明显。nOH 也有类似的结果。结论 在早期疾病的男性患者中,OH与白天嗜睡的相关程度更高,而且在早期帕金森病中,抗胆碱能药物的使用和多巴胺能药物的剂量等处方做法会放大OH与白天嗜睡的相关程度。这种关系与认知能力下降无关。
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Exploring the intersection between orthostatic hypotension and daytime sleepiness in Parkinson disease
Introduction Daytime sleepiness, reported in about 50% of patients with Parkinson disease (PD), is associated with high morbidity, poor quality of life and increased risk for accidents. While an association between dysautonomia and daytime sleepiness in early, de-novo PD has been reported, our understanding of the role of medications, cognitive status and disease duration on this relationship is inadequate. Methods Data were analyzed from the prospective Cincinnati Cohort Biomarkers Program. The primary outcome of interest was daytime sleepiness, as measured by the Epworth Sleepiness Scale (ESS). The primary exposure variable was orthostatic hypotension (OH) with a sub-analysis for the neurogenic OH (nOH) subtype. Regression analyses were carried out adjusting for the following covariates: age, sex, disease duration, education, comorbidities, anti-cholinergic burden, levodopa equivalent dose (LEDD), motor subscore of the Movement disorder society-unified Parkinson disease rating scale, Hoehn and Yahr stage (H&Y), Beck Depression Inventory, and Beck Anxiety Inventory. Results Data on 456 subjects with PD were analyzed. OH was strongly associated with ESS scores, particularly in those with anticholinergic medication use after adjusting for all covariates (RC, 4.30; p<0.001). This adjusted association was more pronounced in men with early disease duration, early H&Y stage, no cognitive decline, and LEDD≤750 mg. Similar results were noted with nOH. Conclusions OH is associated with daytime sleepiness to a greater extent in male patients with early disease and magnified by such prescribing practices as anticholinergic medication use and dopaminergic dosage in early PD. This relationship is independent of cognitive decline.
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