Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Pulmonology, University Hospital Zurich, 8091 Zurich, Switzerland.
Int J Mol Sci. 2022 Nov 14;23(22):14052. doi: 10.3390/ijms232214052.
The direct pathophysiological effects of obstructive sleep apnea (OSA) have been well described. However, the systemic and metabolic consequences of OSA are less well understood. The aim of this secondary analysis was to translate recent findings in healthy subjects on vigilance-state-dependent metabolism into the context of OSA patients and answer the question of how symptomatic OSA influences metabolism and whether these changes might explain metabolic and cardiovascular consequences of OSA. Patients with suspected OSA were assigned according to their oxygen desaturation index (ODI) and Epworth Sleepiness Scale (ESS) score into symptomatic OSA and controls. Vigilance-state-dependent breath metabolites assessed by high-resolution mass spectrometry were used to test for a difference in both groups. In total, 44 patients were eligible, of whom 18 (40.9%) were assigned to the symptomatic OSA group. Symptomatic OSA patients with a median [25%, 75% quartiles] ODI of 40.5 [35.0, 58.8] events/h and an ESS of 14.0 [11.2, 15.8] showed moderate to strong evidence for differences in 18 vigilance-state-dependent breath compounds compared to controls. These identified metabolites are part of major metabolic pathways in carbohydrate, amino acid, and lipid metabolism. Thus, beyond hypoxia per se, we hypothesize that disturbed sleep in OSA patients persists as disturbed sleep-dependent metabolite levels during daytime.
阻塞性睡眠呼吸暂停(OSA)的直接病理生理学效应已有详细描述。然而,OSA 的系统和代谢后果了解较少。本次二次分析的目的是将健康受试者警觉状态依赖性代谢方面的最新发现转化为 OSA 患者的情况,并回答以下问题:有症状的 OSA 如何影响代谢,这些变化是否可以解释 OSA 的代谢和心血管后果。根据其氧减指数(ODI)和嗜睡量表(ESS)评分,将疑似 OSA 的患者分配到有症状的 OSA 组和对照组。使用高分辨率质谱法评估警觉状态依赖性呼吸代谢物,以测试两组之间是否存在差异。共有 44 名患者符合条件,其中 18 名(40.9%)被分配到有症状的 OSA 组。OSA 患者的 ODI 中位数[25%,75%四分位数]为 40.5[35.0,58.8]次/小时,ESS 为 14.0[11.2,15.8],与对照组相比,有中度至强烈的证据表明在 18 种警觉状态依赖性呼吸化合物中存在差异。这些鉴定出的代谢物是碳水化合物、氨基酸和脂质代谢中主要代谢途径的一部分。因此,除了缺氧本身之外,我们假设 OSA 患者的睡眠紊乱在白天仍然表现为睡眠紊乱依赖性代谢物水平。