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羟丁酸钠中的钠:是否值得担忧?

The sodium in sodium oxybate: is there cause for concern?

作者信息

Avidan Alon Y, Kushida Clete A

机构信息

David Geffen School of Medicine at UCLA, 710 Westwood Boulevard, RNRC C153, Los Angeles, 17691, CA, USA.

Stanford University Medical Center, 450 Broadway Street, MC 5704, Pavilion C, 2nd Floor, Redwood City, CA, USA.

出版信息

Sleep Med. 2020 Nov;75:497-501. doi: 10.1016/j.sleep.2020.09.017. Epub 2020 Sep 21.

Abstract

Sodium oxybate (SO), the sodium salt of γ-hydroxybutyric acid, is one of the primary pharmacologic agents used to treat excessive sleepiness, disturbed nighttime sleep, and cataplexy in narcolepsy. The sodium content of SO ranges from 550 to 1640 mg at 3-9 g, given in two equal nightly doses. Clinicians are advised to consider daily sodium intake in patients with narcolepsy who are treated with SO and have comorbid disorders associated with increased cardiovascular (CV) risk, in whom sodium intake may be a concern. It remains unclear whether all patients with narcolepsy treated with SO should modify or restrict their sodium intake. No data are currently available specific to the sodium content or threshold of SO at which patients might experience increased CV risk. To appraise attributable risk, critical evaluation of the literature was conducted to examine the relationship between CV risk and sodium intake, narcolepsy, and SO exposure. The findings suggest that increased CV risk is associated with extremes of daily sodium intake, and that narcolepsy is associated with comorbidities that may increase CV risk in some patients. However, data from studies regarding SO use in patients with narcolepsy have shown a very low frequency of CV side effects (eg, hypertension) and no overall association with CV risk. In the absence of data that specifically address CV risk with SO based on its sodium content, the clinical evidence to date suggests that SO treatment does not confer additional CV risk in patients with narcolepsy.

摘要

羟丁酸钠(SO)是γ-羟基丁酸的钠盐,是用于治疗发作性睡病中过度嗜睡、夜间睡眠障碍和猝倒的主要药物之一。SO的钠含量在3 - 9克时为550至1640毫克,分两个相等的夜间剂量给药。建议临床医生在治疗使用SO且患有与心血管(CV)风险增加相关的合并症的发作性睡病患者时考虑其每日钠摄入量,因为这些患者的钠摄入可能是一个问题。目前尚不清楚所有接受SO治疗的发作性睡病患者是否都应调整或限制其钠摄入量。目前没有关于SO的钠含量或阈值的具体数据,超过该阈值患者可能会出现CV风险增加。为了评估归因风险,对文献进行了批判性评估,以研究CV风险与钠摄入量、发作性睡病和SO暴露之间的关系。研究结果表明,CV风险增加与每日钠摄入量的极端情况有关,发作性睡病与某些患者可能增加CV风险的合并症有关。然而,关于发作性睡病患者使用SO的研究数据显示,CV副作用(如高血压)的发生率非常低,且与CV风险无总体关联。在缺乏基于SO钠含量具体说明CV风险的数据的情况下,迄今为止的临床证据表明,SO治疗不会给发作性睡病患者带来额外的CV风险。

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