The association of objective daytime sleepiness with impaired glucose metabolism in patients with obstructive sleep apnea: a multi-omics study.

IF 5.6 2区 医学 Q1 Medicine Sleep Pub Date : 2024-11-16 DOI:10.1093/sleep/zsae240
Le Chen, Baixin Chen, Yanyuan Dai, Qimeng Sun, Jun Wu, Dandan Zheng, Alexandros N Vgontzas, Xiangdong Tang, Yun Li
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Abstract

Study objectives: To examine the joint effect of obstructive sleep apnea (OSA) and objective excessive daytime sleepiness (EDS) on glucose metabolism and the underlying mechanisms.

Methods: We included 127 patients with OSA. The multiple sleep latency test (MSLT) and Epworth sleepiness scale (ESS) were used to assess objective and subjective EDS, respectively. Disordered glucose metabolism was defined as either a physician diagnosis or having fasting blood glucose levels ≥ 5.6 mmol/L. Values of fasting insulin and homeostasis model assessment of insulin resistance (HOMA-IR) higher than the median values of our sample were defined as high fasting insulin and insulin resistance. Serum metabolomics and fecal microbiota were used to explore underlying mechanisms.

Results: Lower MSLT values were associated with higher levels of fasting blood glucose, fasting insulin, and HOMA-IR. Furthermore, objective EDS was associated with increased odds of disordered glucose metabolism, elevated fasting insulin, and insulin resistance. Dysregulation of serum valine degradation and dysbiosis of fecal Bacteroides thetaiotaomicron were associated with impaired glucose metabolism in OSA with objective EDS. No association between subjective EDS and impaired glucose metabolism was observed.

Conclusion: OSA with objective, but not subjective, EDS is associated with an increased risk of disordered glucose metabolism and insulin resistance. Dysregulation of valine degradation and dysbiosis of Bacteroides thetaiotaomicron appear to link objective EDS and disordered glucose metabolism in OSA.

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阻塞性睡眠呼吸暂停患者白天客观嗜睡与糖代谢受损的关联:一项多组学研究。
研究目的研究阻塞性睡眠呼吸暂停(OSA)和客观白天过度嗜睡(EDS)对糖代谢的共同影响及其内在机制:我们纳入了 127 名 OSA 患者。方法:我们纳入了 127 名 OSA 患者,分别使用多重睡眠潜伏期测试(MSLT)和埃普沃斯嗜睡量表(ESS)评估客观和主观 EDS。经医生诊断或空腹血糖水平≥5.6 mmol/L者为糖代谢紊乱。空腹胰岛素值和胰岛素抵抗稳态模型评估值(HOMA-IR)高于样本的中位值被定义为高空腹胰岛素和胰岛素抵抗。血清代谢组学和粪便微生物群被用来探索潜在的机制:结果:较低的 MSLT 值与较高的空腹血糖、空腹胰岛素和 HOMA-IR 水平相关。此外,客观的 EDS 与葡萄糖代谢紊乱、空腹胰岛素升高和胰岛素抵抗的几率增加有关。血清缬氨酸降解失调和粪便嗜酸乳杆菌(Bacteroides thetaiotaomicron)菌群失调与伴有客观 EDS 的 OSA 患者的糖代谢受损有关。结论:结论:具有客观 EDS 而非主观 EDS 的 OSA 与糖代谢紊乱和胰岛素抵抗的风险增加有关。缬氨酸降解失调和嗜酸乳杆菌(Bacteroides thetaiotaomicron)菌群失调似乎与客观 EDS 和 OSA 葡萄糖代谢紊乱有关。
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来源期刊
Sleep
Sleep Medicine-Neurology (clinical)
CiteScore
8.70
自引率
10.70%
发文量
0
期刊介绍: SLEEP® publishes findings from studies conducted at any level of analysis, including: Genes Molecules Cells Physiology Neural systems and circuits Behavior and cognition Self-report SLEEP® publishes articles that use a wide variety of scientific approaches and address a broad range of topics. These may include, but are not limited to: Basic and neuroscience studies of sleep and circadian mechanisms In vitro and animal models of sleep, circadian rhythms, and human disorders Pre-clinical human investigations, including the measurement and manipulation of sleep and circadian rhythms Studies in clinical or population samples. These may address factors influencing sleep and circadian rhythms (e.g., development and aging, and social and environmental influences) and relationships between sleep, circadian rhythms, health, and disease Clinical trials, epidemiology studies, implementation, and dissemination research.
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