Kheirandish-Gozal Leila
Section of Pediatric Sleep Medicine, Department of Pediatrics, Pritzker School of Medicine, Biological Sciences Division, The University of Chicago Chicago, IL, USA.
Front Neurol. 2012 Jun 11;3:92. doi: 10.3389/fneur.2012.00092. eCollection 2012.
Pediatric sleep disordered breathing has emerged in the last few decades as a highly prevalent condition by virtue of its major morbidities encompassing the central nervous, cardiovascular, and metabolic systems. In this context, improved understanding of the pathophysiological mechanisms underlying the cellular and organ injury and repair mechanisms, and the variance of the phenotype at any level of disease severity is all the more critical if appropriate personalized therapies are to be developed in the future. In this paper, the current evidence and hypothetical framework pointing to the endothelium as a primary cellular target for many of the morbidities of pediatric sleep apnea is reviewed, and particular emphasis on the recruitment of the endothelial cell lineage will be explored. It is hoped that this perspective will foster both expansion and acceleration of discovery efforts aiming to ultimately prevent the potentially lifelong consequences of sleep apnea during childhood.
在过去几十年中,小儿睡眠呼吸障碍已成为一种高度普遍的病症,因为它的主要发病机制涉及中枢神经、心血管和代谢系统。在这种情况下,如果未来要开发适当的个性化疗法,那么更深入地了解细胞和器官损伤及修复机制背后的病理生理机制,以及疾病严重程度任何水平下表型的差异就显得尤为关键。本文回顾了当前的证据和假设框架,这些证据和框架表明内皮细胞是小儿睡眠呼吸暂停许多发病机制的主要细胞靶点,并将特别探讨内皮细胞谱系的募集情况。希望这一观点将促进旨在最终预防儿童期睡眠呼吸暂停潜在终身后果的发现工作的扩展和加速。