Du Zhiyong, Sun Haili, Du Yunhui, Li Linyi, Lv Qianwen, Yu Huahui, Li Fan, Wang Yu, Jiao Xiaolu, Hu Chaowei, Qin Yanwen
The Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, National Clinical Research Center for Cardiovascular Diseases, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing 100029, China.
Antioxidants (Basel). 2022 Sep 29;11(10):1946. doi: 10.3390/antiox11101946.
Obstructive sleep apnea (OSA) can aggravate blood pressure and increase the risk of cardiovascular diseases in hypertensive individuals, yet the underlying pathophysiological process is still incompletely understood. More importantly, OSA remains a significantly undiagnosed condition. In this study, a total of 559 hypertensive patients with and without OSA were included. Metabolome and lipidome-wide analyses were performed to explore the pathophysiological processes of hypertension comorbid OSA and derive potential biomarkers for diagnosing OSA in hypertensive subjects. Compared to non-OSA hypertensive patients (discovery set = 120; validation set = 116), patients with OSA (discovery set = 165; validation set = 158) demonstrated a unique sera metabolic phenotype dominated by abnormalities in biological processes of oxidative stress and inflammation. By integrating three machine learning algorithms, six discriminatory metabolites (including 5-hydroxyeicosatetraenoic acid, taurine, histidine, lysophosphatidic acid 16:0, lysophosphatidylcholine 18:0, and dihydrosphingosine) were selected for constructing diagnostic and classified model. Notably, the established multivariate-model could accurately identify OSA subjects. The corresponding area under the curve values and the correct classification rates were 0.995 and 96.8% for discovery sets, 0.997 and 99.1% for validation sets. This work updates the molecular insights of hypertension comorbid OSA and paves the way for the use of metabolomics for the diagnosis of OSA in hypertensive individuals.
阻塞性睡眠呼吸暂停(OSA)可加重高血压患者的血压,并增加其患心血管疾病的风险,但其潜在的病理生理过程仍未完全明确。更重要的是,OSA仍是一种未得到充分诊断的疾病。在本研究中,共纳入了559例有或无OSA的高血压患者。进行了代谢组和脂质组全分析,以探索高血压合并OSA的病理生理过程,并寻找在高血压患者中诊断OSA的潜在生物标志物。与非OSA高血压患者(发现集=120例;验证集=116例)相比,OSA患者(发现集=165例;验证集=158例)表现出一种独特的血清代谢表型,其主要特征为氧化应激和炎症生物学过程异常。通过整合三种机器学习算法,选择了六种具有鉴别意义的代谢物(包括5-羟基二十碳四烯酸、牛磺酸、组氨酸、溶血磷脂酸16:0、溶血磷脂酰胆碱18:0和二氢鞘氨醇)来构建诊断和分类模型。值得注意的是,所建立的多变量模型能够准确识别OSA患者。发现集的曲线下面积值和正确分类率分别为0.995和96.8%,验证集分别为0.997和99.1%。这项工作更新了结高血压合并OSA的分子认识,并为利用代谢组学诊断高血压患者的OSA铺平了道路。