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阻塞性睡眠呼吸暂停中固有与诱导性环路增益异常

Inherent vs. Induced Loop Gain Abnormalities in Obstructive Sleep Apnea.

作者信息

Deacon-Diaz Naomi, Malhotra Atul

机构信息

Department of Medicine, Pulmonary and Critical Care Medicine, University of California, San Diego, San Diego, CA, United States.

出版信息

Front Neurol. 2018 Nov 2;9:896. doi: 10.3389/fneur.2018.00896. eCollection 2018.

Abstract

Unstable ventilatory chemoreflex control, quantified as loop gain, is recognized as one of four key pathophysiological traits that contribute to cause obstructive sleep apnea (OSA). Novel treatments aimed at reducing loop gain are being investigated, with the intention that future OSA treatment may be tailored to the individual's specific cause of apnea. However, few studies have evaluated loop gain in OSA and non-OSA controls and those that have provide little evidence to support an inherent abnormality in either overall chemical loop gain in OSA patients vs. non-OSA controls, or its components (controller and plant gain). However, intermittent hypoxia may induce high controller gain through neuroplastic changes to chemoreflex control, and may also decrease plant gain via oxidative stress induced inflammation and reduced lung function. The inherent difficulties and limitations with loop gain measurements are discussed and areas where further research are required are highlighted, as only by understanding the mechanisms underlying OSA are new therapeutic approaches likely to emerge in OSA.

摘要

不稳定的通气化学反射控制,以环路增益来量化,被认为是导致阻塞性睡眠呼吸暂停(OSA)的四个关键病理生理特征之一。旨在降低环路增益的新型治疗方法正在研究中,目的是未来的OSA治疗可以根据个体特定的呼吸暂停原因进行定制。然而,很少有研究评估OSA患者和非OSA对照者的环路增益,而那些已有的研究几乎没有提供证据支持OSA患者与非OSA对照者在总体化学环路增益或其组成部分(控制器和对象增益)方面存在内在异常。然而,间歇性缺氧可能通过对化学反射控制的神经可塑性变化诱导高控制器增益,也可能通过氧化应激诱导的炎症和肺功能降低而降低对象增益。本文讨论了环路增益测量存在的固有困难和局限性,并强调了需要进一步研究的领域,因为只有了解OSA的潜在机制,才可能出现OSA的新治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/6224344/fa717577d34b/fneur-09-00896-g0001.jpg

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