Richerson George B, Boison Detlev, Faingold Carl L, Ryvlin Philippe
Departments of Neurology and Molecular Physiology & Biophysics, University of Iowa & Veteran's Affairs Medical Center, Iowa City, Iowa, U.S.A.
Robert Stone Dow Neurobiology Laboratories, Legacy Research Institute Portland, Portland, Oregon, U.S.A.
Epilepsia. 2016 Jan;57 Suppl 1(Suppl 1):35-45. doi: 10.1111/epi.13236.
The mechanisms of sudden unexpected death in epilepsy (SUDEP) have been difficult to define, as most cases occur unwitnessed, and physiologic recordings have been obtained in only a handful of cases. However, recent data obtained from human cases and experimental studies in animal models have brought us closer to identifying potential mechanisms. Theories of SUDEP should be able to explain how a seizure starting in the forebrain can sometimes lead to changes in brainstem cardiorespiratory control mechanisms. Herein we focus on three major themes of work on the causes of SUDEP. First, evidence is reviewed identifying postictal hypoventilation as a major contributor to the cause of death. Second, data are discussed that brainstem serotonin and adenosine pathways may be involved, as well as how they may contribute. Finally, parallels are drawn between SIDS and SUDEP, and we highlight similarities pointing to the possibility of shared pathophysiology involving combined failure of respiratory and cardiovascular control mechanisms. Knowledge about the causes of SUDEP may lead to potential pharmacologic approaches for prevention. We end by describing how translation of this work may result in future applications to clinical care.
癫痫性猝死(SUDEP)的机制一直难以确定,因为大多数病例发生时无目击者在场,且仅在少数病例中获取了生理记录。然而,最近从人类病例和动物模型实验研究中获得的数据使我们更接近确定潜在机制。SUDEP的理论应能够解释始于前脑的癫痫发作有时如何导致脑干心肺控制机制的变化。在此,我们聚焦于关于SUDEP病因的三个主要研究方向。首先,回顾了将发作后通气不足确定为死亡原因主要因素的证据。其次,讨论了脑干5-羟色胺和腺苷通路可能涉及其中以及它们如何发挥作用的数据。最后,比较了婴儿猝死综合征(SIDS)和SUDEP,并强调了相似之处,指出呼吸和心血管控制机制联合衰竭的共同病理生理学可能性。关于SUDEP病因的知识可能会带来潜在的预防药理学方法。我们最后描述了这项研究成果如何转化并应用于未来的临床护理。