Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties

被引:71
作者
von Ellenrieder, Nicolas [1 ]
Dubeau, Francois [1 ]
Gotman, Jean [1 ]
Frauscher, Birgit [1 ,2 ,3 ]
机构
[1] McGill Univ, Montreal Neurol Inst & Hosp, 3801 Univ St, Montreal, PQ H3A 2B4, Canada
[2] Queens Univ, Dept Med, Botterell Hall,Room 233,18 Stuart St, Kingston, ON K7L 3N6, Canada
[3] Queens Univ, Ctr Neurosci Studies, Botterell Hall,Room 233,18 Stuart St, Kingston, ON K7L 3N6, Canada
基金
奥地利科学基金会; 加拿大健康研究院;
关键词
Epilepsy; Intracerebral EEG; Polysomnography; High frequency oscillations; Sleep; MEDIAL TEMPORAL-LOBE; EYE-MOVEMENT SLEEP; SEIZURE-ONSET ZONE; SLOW WAVES; DEPENDENT PLASTICITY; EPILEPTIC ACTIVITY; EEG; SYNCHRONIZATION; ACTIVATION; MECHANISMS;
D O I
10.1016/j.nicl.2017.02.018
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
Objective: The stage of sleep is a known modulator of high-frequency oscillations (HFOs). For instance, high amplitude slow waves during NREM sleep and the subtypes of REM sleep were shown to contribute to a better separation between physiological and pathological HFOs. This study investigated rates and spatial spread of the different HFO types (physiological and pathological ripples in the 80-250 Hz frequency band, and fast ripples above 250 Hz) depending on time spent in sleep across the different sleep cycles. Methods: Fifteen patients with focal pharmaco-resistant epilepsy underwent one night of video-polysomnography during chronic intracranial EEG recording for presurgical epilepsy evaluation. The HFO rate and spread across the different sleep cycles were determined with an automatic HFO detector. We built models to explain the observed rate and spread based on time in sleep and other variables i.e. sleep stage, delta band and sigma band activity, and slow wave amplitude. Statistical significance of the different variables was determined by a model comparison using the Akaike information criterion. Results: The rate of HFOs depends significantly on the accumulated time of sleep. As the night advanced, the rate of pathological ripples and fast ripples decreased during NREM sleep (up to 15% per hour spent in the respective sleep stages), while the rate of physiological ripples increased during REM sleep (8% per hour spent in REM sleep). Interestingly, the stage of sleep but not the sleep cycle determined the extent of spread of HFOs, showing a larger field during NREM sleep and a more restricted field during REM sleep. Conclusion: The different dependence with sleep time for physiological and pathological ripples is in keeping with their distinct underlying generating mechanisms. From a practical point of view, the first sleep cycle seems to be best suitable for studying HFOs in epilepsy, given that the contrast between physiological and pathological ripple rates is largest during this time. (C) 2017 The Authors. Published by Elsevier Inc.
引用
收藏
页码:566 / 573
页数:8
相关论文
共 35 条
[1]   The spatial and signal characteristics of physiologic high frequency oscillations [J].
Alkawadri, Rafeed ;
Gaspard, Nicolas ;
Goncharova, Irina I. ;
Spencer, Dennis D. ;
Gerrard, Jason L. ;
Zaveri, Hitten ;
Duckrow, Robert B. ;
Blumenfeld, Hal ;
Hirsch, Lawrence J. .
EPILEPSIA, 2014, 55 (12) :1986-1995
[2]  
[Anonymous], 2002, Model selection and multimodel inference: a practical informationtheoretic approach
[3]   Ripples in the medial temporal lobe are relevant for human memory consolidation [J].
Axmacher, Nikolai ;
Elger, Christian E. ;
Fell, Juergen .
BRAIN, 2008, 131 :1806-1817
[4]   Effect of sleep stage on interictal high-frequency oscillations recorded from depth macroelectrodes in patients with focal epilepsy [J].
Bagshaw, Andrew P. ;
Jacobs, Julia ;
LeVan, Pierre ;
Dubeau, Francois ;
Gotman, Jean .
EPILEPSIA, 2009, 50 (04) :617-628
[5]  
Berry R., 2017, The AASM Manual for the Scoring of Sleep and Associated Events: Rules, Terminology and Technical Specifications
[6]   Data mining neocortical high-frequency oscillations in epilepsy and controls [J].
Blanco, Justin A. ;
Stead, Matt ;
Krieger, Abba ;
Stacey, William ;
Maus, Douglas ;
Marsh, Eric ;
Viventi, Jonathan ;
Lee, Kendall H. ;
Marsh, Richard ;
Litt, Brian ;
Worrell, Gregory A. .
BRAIN, 2011, 134 :2948-2959
[7]   HIGH-FREQUENCY NETWORK OSCILLATION IN THE HIPPOCAMPUS [J].
BUZSAKI, G ;
HORVATH, Z ;
URIOSTE, R ;
HETKE, J ;
WISE, K .
SCIENCE, 1992, 256 (5059) :1025-1027
[8]   Activation of phasic pontine-wave generator prevents rapid eye movement sleep deprivation-induced learning impairment in the rat: A mechanism for sleep-dependent plasticity [J].
Datta, S ;
Mavanji, V ;
Ulloor, J ;
Patterson, EH .
JOURNAL OF NEUROSCIENCE, 2004, 24 (06) :1416-1427
[9]   Avoidance task training potentiates phasic pontine-wave density in the rat: A mechanism for sleep-dependent plasticity [J].
Datta, S .
JOURNAL OF NEUROSCIENCE, 2000, 20 (22) :8607-8613
[10]   The whats and whens of sleep-dependent memory consolidation [J].
Diekelmann, Susanne ;
Wilhelm, Ines ;
Born, Jan .
SLEEP MEDICINE REVIEWS, 2009, 13 (05) :309-321