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Urinary metabolite signatures reflect the altered host metabolism in severe obstructive sleep apnea

代谢组学 阻塞性睡眠呼吸暂停 代谢物 谷氨酰胺 化学 代谢途径 尿 气体分析呼吸 香草扁桃酸 气相色谱-质谱法 多导睡眠图 内科学 生物标志物 内分泌学 医学 新陈代谢 生物化学 质谱法 氨基酸 色谱法 高香草酸 呼吸暂停 受体 血清素
作者
Mohit Mohit,Manendra Singh Tomar,Fabrizio Araniti,Prabhat Kumar Sahai,Bhanu Pratap Singh,Ashutosh Shrivastava,Pooran Chand
出处
期刊:Journal of Chromatography B [Elsevier BV]
卷期号:1231: 123938-123938 被引量:1
标识
DOI:10.1016/j.jchromb.2023.123938
摘要

Obstructive sleep apnea (OSA) is a common sleep-related breathing disorder. The onset and progression of OSA are often linked with severe cardiovascular and metabolic comorbidities. At the same time, given the increasing prevalence of OSA, novel methods to screen OSA and its follow-up are needed. Untargeted metabolic profiling of OSA patients and healthy controls was planned to capture a snapshot of urinary metabolites and potential biomarkers using the gas chromatography-mass spectrometry (GC–MS) method. Polysomnography (PSG) confirmed severe OSA patients with AHI index ≥ 30 were considered for urine sample collection. The sample size was constituted of OSA (n = 36) and healthy controls (n = 36). Metabolite extraction and derivatization were performed and metabolomic analysis was performed by using GC–MS. The obtained data set was statistically analyzed using univariate and multivariate analysis. The Orthogonal partial least-squares discriminant analysis (OPLS-DA) was performed to screen differential metabolites between OSA patients and healthy controls. The metabolomic analysis revealed a total of 142 significantly altered metabolites of interest. Biomarker analysis allows for the creation of a list of putative urinary biomarkers including GABA, malic acid, glutamic acid, epichoric acid etc., with an accuracy of 99.8 % to 100 % for OSA screening. Subsequently, pathway analysis revealed that related biochemical pathways like the tricarboxylic acid cycle (TCA), glutamate/glutamine, amino acid and fatty acid metabolism, that are significantly interlinked with these metabolic biomarkers can play a crucial role in the pathogenesis of OSA. This study paves the way to undertake mass screening in a larger population to identify specific and reliable biomarkers.
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