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呼吸暂停低通气指数和阻塞性睡眠呼吸暂停的蛋白质组学生物标志物:对存在、严重程度和治疗反应的病理生理学的深入了解。

Proteomic Biomarkers of the Apnea Hypopnea Index and Obstructive Sleep Apnea: Insights into the Pathophysiology of Presence, Severity, and Treatment Response.

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University, 3165 Porter Drive, Stanford, CA 94304, USA.

Biomedical Signal Processing & AI Research Group, Department of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.

出版信息

Int J Mol Sci. 2022 Jul 20;23(14):7983. doi: 10.3390/ijms23147983.

DOI:10.3390/ijms23147983
PMID:35887329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9317550/
Abstract

Obstructive sleep apnea (OSA), a disease associated with excessive sleepiness and increased cardiovascular risk, affects an estimated 1 billion people worldwide. The present study examined proteomic biomarkers indicative of presence, severity, and treatment response in OSA. Participants (n = 1391) of the Stanford Technology Analytics and Genomics in Sleep study had blood collected and completed an overnight polysomnography for scoring the apnea−hypopnea index (AHI). A highly multiplexed aptamer-based array (SomaScan) was used to quantify 5000 proteins in all plasma samples. Two separate intervention-based cohorts with sleep apnea (n = 41) provided samples pre- and post-continuous/positive airway pressure (CPAP/PAP). Multivariate analyses identified 84 proteins (47 positively, 37 negatively) associated with AHI after correction for multiple testing. Of the top 15 features from a machine learning classifier for AHI ≥ 15 vs. AHI < 15 (Area Under the Curve (AUC) = 0.74), 8 were significant markers of both AHI and OSA from multivariate analyses. Exploration of pre- and post-intervention analysis identified 5 of the 84 proteins to be significantly decreased following CPAP/PAP treatment, with pathways involving endothelial function, blood coagulation, and inflammatory response. The present study identified PAI-1, tPA, and sE-Selectin as key biomarkers and suggests that endothelial dysfunction and increased coagulopathy are important consequences of OSA, which may explain the association with cardiovascular disease and stroke.

摘要

阻塞性睡眠呼吸暂停(OSA)是一种与过度嗜睡和心血管风险增加相关的疾病,估计影响全球 10 亿人。本研究探讨了提示 OSA 存在、严重程度和治疗反应的蛋白质组学生物标志物。斯坦福技术分析和睡眠基因组学研究的参与者(n=1391)采集血液并完成整夜多导睡眠图以评分呼吸暂停-低通气指数(AHI)。使用高度多重化的基于适配体的阵列(SomaScan)定量所有血浆样本中的 5000 种蛋白质。两个单独的基于干预的睡眠呼吸暂停队列(n=41)提供了 CPAP/PAP 治疗前后的样本。多变量分析鉴定出 84 种蛋白质(47 种阳性,37 种阴性)与 AHI 相关,经多重检验校正后。在 AHI≥15 与 AHI<15 的机器学习分类器的前 15 个特征中(曲线下面积(AUC)=0.74),有 8 个是 AHI 和 OSA 的重要标志物来自多变量分析。干预前和干预后分析的探索确定了 84 种蛋白质中的 5 种在 CPAP/PAP 治疗后显著降低,涉及内皮功能、血液凝固和炎症反应的途径。本研究确定了 PAI-1、tPA 和 sE-选择素作为关键生物标志物,并表明内皮功能障碍和凝血功能亢进是 OSA 的重要后果,这可能解释了与心血管疾病和中风的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/cd6645ca6171/ijms-23-07983-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/3a84ca81e411/ijms-23-07983-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/c38cbbedd3cc/ijms-23-07983-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/cd6645ca6171/ijms-23-07983-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/3a84ca81e411/ijms-23-07983-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/c38cbbedd3cc/ijms-23-07983-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/9317550/cd6645ca6171/ijms-23-07983-g003.jpg

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