胰岛素抵抗
阻塞性睡眠呼吸暂停
内科学
内分泌学
碳水化合物代谢
白天过度嗜睡
胰岛素
医学
糖代谢紊乱
睡眠障碍
精神科
认知
作者
Le Chen,Baixin Chen,Yanyuan Dai,Qimeng Sun,Jun Wu,Dandan Zheng,Alexandros N. Vgontzas,Xiangdong Tang,Yun Li
出处
期刊:Sleep
[Oxford University Press]
日期:2024-11-16
标识
DOI:10.1093/sleep/zsae240
摘要
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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