• Something wrong with this record ?

Sleep Disruption in Epilepsy: Ictal and Interictal Epileptic Activity Matter

L. Peter-Derex, P. Klimes, V. Latreille, S. Bouhadoun, F. Dubeau, B. Frauscher,

. 2020 ; 88 (5) : 907-920. [pub] 20200921

Language English Country United States

Document type Journal Article, Research Support, Non-U.S. Gov't

OBJECTIVE: Disturbed sleep is common in epilepsy. The direct influence of nocturnal epileptic activity on sleep fragmentation remains poorly understood. Stereo-electroencephalography paired with polysomnography is the ideal tool to study this relationship. We investigated whether sleep-related epileptic activity is associated with sleep disruption. METHODS: We visually marked sleep stages, arousals, seizures, and epileptic bursts in 36 patients with focal drug-resistant epilepsy who underwent combined stereo-electroencephalography/polysomnography during presurgical evaluation. Epileptic spikes were detected automatically. Spike and burst indices (n/sec/channel) were computed across four 3-second time windows (baseline sleep, pre-arousal, arousal, and post-arousal). Sleep stage and anatomic localization were tested as modulating factors. We assessed the intra-arousal dynamics of spikes and their relationship with the slow wave component of non-rapid eye-movement sleep (NR) arousals. RESULTS: The vast majority of sleep-related seizures (82.4%; 76.5% asymptomatic) were followed by awakenings or arousals. The epileptic burst index increased significantly before arousals as compared to baseline and postarousal, irrespective of sleep stage or brain area. A similar pre-arousal increase was observed for the spike index in NR stage 2 and rapid eye-movement sleep. In addition, the spike index increased during the arousal itself in neocortical channels, and was strongly correlated with the slow wave component of NR arousals (r = 0.99, p < 0.0001). INTERPRETATION: Sleep fragmentation in focal drug-resistant epilepsy is associated with ictal and interictal epileptic activity. The increase in interictal epileptic activity before arousals suggests its participation in sleep disruption. An additional increase in the spike rate during arousals may result from a sleep-wake boundary instability, suggesting a bidirectional relationship. ANN NEUROL 2020;88:907-920.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20027657
003      
CZ-PrNML
005      
20210114152210.0
007      
ta
008      
210105s2020 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1002/ana.25884 $2 doi
035    __
$a (PubMed)32833279
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Peter-Derex, Laure $u Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada. Center for Sleep Medicine and Respiratory Diseases, Lyon University Hospital, Lyon 1 University, Lyon, France. Lyon Neuroscience Research Center, CNRS UMR5292 / INSERM, U1028, Lyon, France.
245    10
$a Sleep Disruption in Epilepsy: Ictal and Interictal Epileptic Activity Matter / $c L. Peter-Derex, P. Klimes, V. Latreille, S. Bouhadoun, F. Dubeau, B. Frauscher,
520    9_
$a OBJECTIVE: Disturbed sleep is common in epilepsy. The direct influence of nocturnal epileptic activity on sleep fragmentation remains poorly understood. Stereo-electroencephalography paired with polysomnography is the ideal tool to study this relationship. We investigated whether sleep-related epileptic activity is associated with sleep disruption. METHODS: We visually marked sleep stages, arousals, seizures, and epileptic bursts in 36 patients with focal drug-resistant epilepsy who underwent combined stereo-electroencephalography/polysomnography during presurgical evaluation. Epileptic spikes were detected automatically. Spike and burst indices (n/sec/channel) were computed across four 3-second time windows (baseline sleep, pre-arousal, arousal, and post-arousal). Sleep stage and anatomic localization were tested as modulating factors. We assessed the intra-arousal dynamics of spikes and their relationship with the slow wave component of non-rapid eye-movement sleep (NR) arousals. RESULTS: The vast majority of sleep-related seizures (82.4%; 76.5% asymptomatic) were followed by awakenings or arousals. The epileptic burst index increased significantly before arousals as compared to baseline and postarousal, irrespective of sleep stage or brain area. A similar pre-arousal increase was observed for the spike index in NR stage 2 and rapid eye-movement sleep. In addition, the spike index increased during the arousal itself in neocortical channels, and was strongly correlated with the slow wave component of NR arousals (r = 0.99, p < 0.0001). INTERPRETATION: Sleep fragmentation in focal drug-resistant epilepsy is associated with ictal and interictal epileptic activity. The increase in interictal epileptic activity before arousals suggests its participation in sleep disruption. An additional increase in the spike rate during arousals may result from a sleep-wake boundary instability, suggesting a bidirectional relationship. ANN NEUROL 2020;88:907-920.
650    _2
$a dospělí $7 D000328
650    _2
$a arousal $7 D001143
650    _2
$a refrakterní epilepsie $7 D000069279
650    _2
$a elektroencefalografie $7 D004569
650    _2
$a epilepsie $x komplikace $7 D004827
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a polysomnografie $7 D017286
650    _2
$a záchvaty $x komplikace $7 D012640
650    _2
$a spánková deprivace $x etiologie $7 D012892
650    _2
$a stadia spánku $7 D012894
650    _2
$a poruchy spánku a bdění $x etiologie $7 D012893
650    _2
$a spánek pomalých vln $7 D000077310
650    _2
$a mladý dospělý $7 D055815
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Klimes, Petr $u Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada. Institute of Scientific Instruments, The Czech Academy of Sciences, Brno, Czech Republic.
700    1_
$a Latreille, Véronique $u Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada.
700    1_
$a Bouhadoun, Sarah $u Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada.
700    1_
$a Dubeau, François $u Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada.
700    1_
$a Frauscher, Birgit $u Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada.
773    0_
$w MED00000428 $t Annals of neurology $x 1531-8249 $g Roč. 88, č. 5 (2020), s. 907-920
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32833279 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20210105 $b ABA008
991    __
$a 20210114152208 $b ABA008
999    __
$a ok $b bmc $g 1607992 $s 1118837
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 88 $c 5 $d 907-920 $e 20200921 $i 1531-8249 $m Annals of neurology $n Ann Neurol $x MED00000428
LZP    __
$a Pubmed-20210105

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...