Neuropediatrics 2015; 46(03): 171-180
DOI: 10.1055/s-0035-1551574
Review Article
Georg Thieme Verlag KG Stuttgart · New York

Sleep and Epilepsy Syndromes

Bernhard Schmitt
1   Division of Clinical Neurophysiology and Epilepsy, University Children's Hospital, Zurich, Switzerland
› Institutsangaben
Weitere Informationen

Publikationsverlauf

14. Dezember 2014

14. April 2015

Publikationsdatum:
12. Mai 2015 (online)

Abstract

Sleep and epilepsy have a close relationship. About 20% of patients suffer seizures only during the night, approximately 40% only during the day and approximately 35% during the day and night. In certain epilepsy syndromes, the occurrence of seizures is strongly related to sleep or awakening. Infantile spasms appear predominately on awakening, and hypsarrhythmia is sometimes visible only in sleep. Children with Panayiotopoulos syndrome or benign epilepsy with centrotemporal spikes (BECTS) have seizures mostly when asleep, and in both syndromes interictal spike waves are markedly accentuated in slow wave sleep. Electrical status epilepticus during slow sleep/continuous spike wave discharges during sleep (ESES/CSWS), atypical benign partial epilepsy, and Landau–Kleffner syndrome are epileptic encephalopathies with substantial behavioral and cognitive deficits, various seizures, and continuous spike–wave activity during non–rapid eye movement (NREM) sleep. The hallmark of juvenile myoclonic epilepsy and grand mal seizures on awakening are seizure symptoms within 2 hours after awakening, often provoked by sleep deprivation. Nocturnal frontal lobe epilepsy is sometimes mistaken for parasomnia. Differentiation is possible when the clinical symptoms and the frequency of the paroxysmal events per night and month are carefully observed and nocturnal video electroencephalography (EEG) performed. Sleep EEG recordings may be helpful in patients with suspected epilepsy and nonconclusive awake EEG. Depending on the clinical question, sleep recordings should be performed during nap (natural sleep or drug induced), during the night, or after sleep deprivation.

 
  • References

  • 1 Dinner DS, Lüders HO. Relationship of epilepsy and sleep: overview. In: Dinner DS, Lüders HO, , eds. Epilepsy and sleep. Physiological and Clinical Relationships. San Diego, CA: Academic Press; 2001: 2-18
  • 2 Shewmon DW. Ictal aspects with emphasis on unusual variants. In: Dulac O, Chugani HT, Dalla Bernardina B, , eds. Infantile Spasms and West Syndrome. London: WB Saunders Company; 1994: 36-51
  • 3 Watanabe K, Negoro T, Aso K, Matsumoto A. Reappraisal of interictal electroencephalograms in infantile spasms. Epilepsia 1993; 34 (4) 679-685
  • 4 O'Callaghan FJ, Lux AL, Darke K , et al. The effect of lead time to treatment and of age of onset on developmental outcome at 4 years in infantile spasms: evidence from the United Kingdom Infantile Spasms Study. Epilepsia 2011; 52 (7) 1359-1364
  • 5 Rating D, Seidel U, Grimm B, Hanefeld F. The prognostic value of EEG patterns in epilepsies with infantile spasms. Brain Dev 1987; 9 (4) 361-364
  • 6 Kramer U, Sue WC, Mikati MA. Hypsarrhythmia: frequency of variant patterns and correlation with etiology and outcome. Neurology 1997; 48 (1) 197-203
  • 7 Fattinger S, Schmitt B, Bölsterli Heinzle BK, Critelli H, Jenni OG, Huber R. Impaired slow wave sleep downscaling in patients with infantile spasms. Eur J Paediatr Neurol 2015; 19 (2) 134-142
  • 8 Hancock EC, Osborne JP, Edwards SW. Treatment of infantile spasms. Cochrane Database Syst Rev 2013; 6: CD001770
  • 9 Go CY, Mackay MT, Weiss SK , et al; Child Neurology Society; American Academy of Neurology; Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Evidence-based guideline update: medical treatment of infantile spasms. Neurology 2012; 78 (24) 1974-1980
  • 10 Panayiotopoulos CP, Michael M, Sanders S, Valeta T, Koutroumanidis M. Benign childhood focal epilepsies: assessment of established and newly recognized syndromes. Brain 2008; 131 (Pt 9) 2264-2286
  • 11 Specchio N, Trivisano M, Di Ciommo V , et al. Panayiotopoulos syndrome: a clinical, EEG, and neuropsychological study of 93 consecutive patients. Epilepsia 2010; 51 (10) 2098-2107
  • 12 Koutroumanidis M, Ferrie CD, Valeta T, Sanders S, Michael M, Panayiotopoulos CP. Syncope-like epileptic seizures in Panayiotopoulos syndrome. Neurology 2012; 79 (5) 463-467
  • 13 Caraballo R, Cersósimo R, Fejerman N. Panayiotopoulos syndrome: a prospective study of 192 patients. Epilepsia 2007; 48 (6) 1054-1061
  • 14 Specchio N, Trivisano M, Claps D, Battaglia D, Fusco L, Vigevano F. Documentation of autonomic seizures and autonomic status epilepticus with ictal EEG in Panayiotopoulos syndrome. Epilepsy Behav 2010; 19 (3) 383-393
  • 15 Lerman P. Benign partial epilepsy with centro-temporal spikes. In: Roger J, Dravet C, Bureau M, Dreifuss FE, Wolf P, , eds. Epileptic Syndromes in Infancy, Childhood and Adolescence. London and Paris: John Libbey Eurotext Ltd; 1985: 150-158
  • 16 Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for classification of epilepsies and epileptic syndromes. Epilepsia 1985; 26 (3) 268-278
  • 17 Loiseau P, Beaussart M. The seizures of benign childhood epilepsy with Rolandic paroxysmal discharges. Epilepsia 1973; 14 (4) 381-389
  • 18 Eeg-Olofsson O. Rolandic epilepsy. In: Bazil CW, Malow BA, Sammaritano MR, , eds. Sleep and Epilepsy: The Clinical Spectrum. Amsterdam: Elsevier; 2002: 257-263
  • 19 Glauser T, Ben-Menachem E, Bourgeois B , et al; ILAE Subcommission on AED Guidelines. Updated ILAE evidence review of antiepileptic drug efficacy and effectiveness as initial monotherapy for epileptic seizures and syndromes. Epilepsia 2013; 54 (3) 551-563
  • 20 Lerman P, Kivity S. Benign focal epilepsy of childhood. A follow-up study of 100 recovered patients. Arch Neurol 1975; 32 (4) 261-264
  • 21 Doose H, Baier WK. Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation. Eur J Pediatr 1989; 149 (3) 152-158
  • 22 Lemke JR, Lal D, Reinthaler EM , et al. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat Genet 2013; 45 (9) 1067-1072
  • 23 Nicolai J, van der Linden I, Arends JB , et al. EEG characteristics related to educational impairments in children with benign childhood epilepsy with centrotemporal spikes. Epilepsia 2007; 48 (11) 2093-2100
  • 24 Binnie CD. Significance and management of transitory cognitive impairment due to subclinical EEG discharges in children. Brain Dev 1993; 15 (1) 23-30
  • 25 Patry G, Lyagoubi S, Tassinari CA. Subclinical “electrical status epilepticus” induced by sleep in children. A clinical and electroencephalographic study of six cases. Arch Neurol 1971; 24 (3) 242-252
  • 26 Morikawa T, Seino M, Osawa T, Yagi K. Five children with continuous spike-wave discharges during sleep. In: Roger J, Dravet C, Bureau M, Dreifuss FE, Wolf P, , eds. Epileptic Syndromes in Infancy, Childhood and Adolescence. London and Paris: John Libbey Eurotext Ltd; 1985: 205-212
  • 27 Carvill GL, Regan BM, Yendle SC , et al. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. Nat Genet 2013; 45 (9) 1073-1076
  • 28 Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989; 30 (4) 389-399
  • 29 Tassinari CA, Rubboli G, Volpi L, Billard C, Bureau M. Electrical status epilepticus during slow sleep (ESES or CSWS) including acquired epileptic aphasia (Landau-Kleffner syndrome). In: Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, , eds. Epileptic Syndromes in Infancy, Childhood and Adolescence. London and Paris: John Libbey Eurotext Ltd; 2005: 295-314
  • 30 Roulet Perez E, Davidoff V, Despland PA, Deonna T. Mental and behavioural deterioration of children with epilepsy and CSWS: acquired epileptic frontal syndrome. Dev Med Child Neurol 1993; 35 (8) 661-674
  • 31 Galanopoulou AS, Bojko A, Lado F, Moshé SL. The spectrum of neuropsychiatric abnormalities associated with electrical status epilepticus in sleep. Brain Dev 2000; 22 (5) 279-295
  • 32 Schmitt B, Wohlrab G. EEG in der Neuropädiatrie. Berlin Heidelberg: Springer-Verlag; 2013
  • 33 Scheltens-de Boer M. Guidelines for EEG in encephalopathy related to ESES/CSWS in children. Epilepsia 2009; 50 (Suppl. 07) 13-17
  • 34 Aeby A, Poznanski N, Verheulpen D, Wetzburger C, Van Bogaert P. Levetiracetam efficacy in epileptic syndromes with continuous spikes and waves during slow sleep: experience in 12 cases. Epilepsia 2005; 46 (12) 1937-1942
  • 35 Guzzetta F, Battaglia D, Veredice C , et al. Early thalamic injury associated with epilepsy and continuous spike-wave during slow sleep. Epilepsia 2005; 46 (6) 889-900
  • 36 Bölsterli BK, Schmitt B, Bast T , et al. Impaired slow wave sleep downscaling in encephalopathy with status epilepticus during sleep (ESES). Clin Neurophysiol 2011; 122 (9) 1779-1787
  • 37 Bölsterli Heinzle BK, Fattinger S, Kurth S , et al. Spike wave location and density disturb sleep slow waves in patients with CSWS (continuous spike waves during sleep). Epilepsia 2014; 55 (4) 584-591
  • 38 Siniatchkin M, Groening K, Moehring J , et al. Neuronal networks in children with continuous spikes and waves during slow sleep. Brain 2010; 133 (9) 2798-2813
  • 39 Veggiotti P, Pera MC, Teutonico F, Brazzo D, Balottin U, Tassinari CA. Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update. Epileptic Disord 2012; 14 (1) 1-11
  • 40 Pera MC, Brazzo D, Altieri N, Balottin U, Veggiotti P. Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: a variable prognosis. Epilepsia 2013; 54 (Suppl. 07) 77-85
  • 41 Seegmüller C, Deonna T, Dubois CM , et al. Long-term outcome after cognitive and behavioral regression in nonlesional epilepsy with continuous spike-waves during slow-wave sleep. Epilepsia 2012; 53 (6) 1067-1076
  • 42 Aicardi J, Chevrie JJ. Atypical benign partial epilepsy of childhood. Dev Med Child Neurol 1982; 24 (3) 281-292
  • 43 Doose H. Symptomatology in children with focal sharp waves of genetic origin. Eur J Pediatr 1989; 149 (3) 210-215
  • 44 Hahn A. Atypical benign partial epilepsy/pseudo-Lennox syndrome. Epileptic Disord 2000; 2 (Suppl. 01) S11-S17
  • 45 Landau WM, Kleffner FR. Syndrome of acquired aphasia with convulsive disorder in children. Neurology 1957; 7 (8) 523-530
  • 46 Caraballo RH, Cejas N, Chamorro N, Kaltenmeier MC, Fortini S, Soprano AM. Landau-Kleffner syndrome: a study of 29 patients. Seizure 2014; 23 (2) 98-104
  • 47 Deonna TW. Acquired epileptiform aphasia in children (Landau-Kleffner syndrome). J Clin Neurophysiol 1991; 8 (3) 288-298
  • 48 Janz D, Christian W. Impulsiv-Petit mal. Dtsch Z Nervenheilkd 1957; 176 (3) 346-386
  • 49 Genton P, Thomas P, Kasteleijn-Nolst Trenité DG, Medina MT, Salas-Puig J. Clinical aspects of juvenile myoclonic epilepsy. Epilepsy Behav 2013; 28 (Suppl. 01) S8-S14
  • 50 Kasteleijn-Nolst Trenité DG, Schmitz B, Janz D , et al. Consensus on diagnosis and management of JME: From founder's observations to current trends. Epilepsy Behav 2013; 28 (Suppl. 01) S87-S90
  • 51 Mayer TA, Schroeder F, May TW, Wolf PT. Perioral reflex myoclonias: a controlled study in patients with JME and focal epilepsies. Epilepsia 2006; 47 (6) 1059-1067
  • 52 Thomas P, Genton P, Gelisse P, Wolf P. Juvenile myoclonic epilepsy. In: Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, , eds. Epileptic Syndromes in Infancy, Childhood and Adolescence. London and Paris: John Libbey Eurotext Ltd; 2005: 367-388
  • 53 Serafini A, Rubboli G, Gigli GL, Koutroumanidis M, Gelisse P. Neurophysiology of juvenile myoclonic epilepsy. Epilepsy Behav 2013; 28 (Suppl. 01) S30-S39
  • 54 Schmitz B, Yacubian EM, Feucht M, Hermann B, Trimble M. Neuropsychology and behavior in juvenile myoclonic epilepsy. Epilepsy Behav 2013; 28 (Suppl. 01) S72-S73
  • 55 Crespel A, Gelisse P, Reed RC , et al. Management of juvenile myoclonic epilepsy. Epilepsy Behav 2013; 28 (Suppl. 01) S81-S86
  • 56 Senf P, Schmitz B, Holtkamp M, Janz D. Prognosis of juvenile myoclonic epilepsy 45 years after onset: seizure outcome and predictors. Neurology 2013; 81 (24) 2128-2133
  • 57 Janz D. Epilepsy with grand mal on awakening and sleep-waking cycle. Clin Neurophysiol 2000; 111 (Suppl. 02) S103-S110
  • 58 Genton P, Gonzales Sanchez M, Thomas P. Epilepsy with Grand Mal on awakening. In: Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, , eds. Epileptic Syndromes in Infancy, Childhood and Adolescence. London and Paris: John Libbey Eurotext Ltd; 2005: 389-394
  • 59 Holtkamp M, Kowski AB, Merkle H, Janz D. Long-term outcome in epilepsy with grand mal on awakening: forty years of follow-up. Ann Neurol 2014; 75 (2) 298-302
  • 60 Derry CP. Sleeping in fits and starts: a practical guide to distinguishing nocturnal epilepsy from sleep disorders. Pract Neurol 2014; 14 (6) 391-398
  • 61 Provini F, Plazzi G, Tinuper P, Vandi S, Lugaresi E, Montagna P. Nocturnal frontal lobe epilepsy. A clinical and polygraphic overview of 100 consecutive cases. Brain 1999; 122 (Pt 6) 1017-1031
  • 62 Scheffer IE, Bhatia KP, Lopes-Cendes I , et al. Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder. Brain 1995; 118 (Pt 1) 61-73
  • 63 Heron SE, Smith KR, Bahlo M , et al. Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet 2012; 44 (11) 1188-1190
  • 64 Picard F, Makrythanasis P, Navarro V , et al. DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy. Neurology 2014; 82 (23) 2101-2106