Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies

András Horváth,1,2 Anikó Papp,1 Anna Szűcs,1 1Department of Neurology, National Institute of Clinical Neurosciences, 2János Szentágothai Doctoral School of Neurosciences, Semmelweis University School of PhD Studies, Budapest, Hungary A...

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Autores principales: Horváth A, Papp A, Szűcs A
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:658d3f50ed5b41628f8ffc398a65b5752021-12-02T01:58:03ZProgress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies1179-1608https://doaj.org/article/658d3f50ed5b41628f8ffc398a65b5752016-03-01T00:00:00Zhttps://www.dovepress.com/progress-in-elucidating-the-pathophysiological-basis-of-nonrapid-eye-m-peer-reviewed-article-NSShttps://doaj.org/toc/1179-1608András Horváth,1,2 Anikó Papp,1 Anna Szűcs,1 1Department of Neurology, National Institute of Clinical Neurosciences, 2János Szentágothai Doctoral School of Neurosciences, Semmelweis University School of PhD Studies, Budapest, Hungary Abstract: Nonrapid eye movement (NREM) or arousal parasomnias are prevalent conditions in children and young adults, apparently provoked by any medical, physical, mental, or pharmacologic/toxic agent disturbing normal biorhythm and causing sleep fragmentation or abundant amount of slow wave sleep. The nadir and the ascending slope of the first sleep cycle of night sleep are the typical periods when NREM parasomnias, especially sleepwalking may occur on sleep-microstructural level; microarousals are the typical moments allowing NREM parasomnias. While sleep-disturbing factors have a clear precipitating effect, a genetic predisposition appears necessary in most cases. A candidate gene for sleepwalking has been identified on chromosome 20q12-q13.12 in one sleepwalking family. NREM parasomnias have a genetic and clinical link with nocturnal-frontal lobe epilepsies; possibly through an abnormality of the acetylcholine-related sleep-control system. The association of NREM parasomnias with the human leukocyte antigen system might be the sign of an autoimmune background to be further clarified. In the treatment of arousal parasomnias, the main tools are adequate sleep hygiene and the management of underlying conditions. Their pharmacotherapy has remained unresolved; the best options are clonazepam and some of the antidepressants, while a psychotherapy approach is also justified. Keywords: sleep disorders, arousal disorders, NREM parasomnia, sleepwalking, sleep terrorHorváth APapp ASzűcs ADove Medical Pressarticlesleep disordersarousal disordersNREM parasomniasleep walkingsleep terrorPsychiatryRC435-571Neurophysiology and neuropsychologyQP351-495ENNature and Science of Sleep, Vol 2016, Iss Issue 1, Pp 73-79 (2016)
institution DOAJ
collection DOAJ
language EN
topic sleep disorders
arousal disorders
NREM parasomnia
sleep walking
sleep terror
Psychiatry
RC435-571
Neurophysiology and neuropsychology
QP351-495
spellingShingle sleep disorders
arousal disorders
NREM parasomnia
sleep walking
sleep terror
Psychiatry
RC435-571
Neurophysiology and neuropsychology
QP351-495
Horváth A
Papp A
Szűcs A
Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
description András Horváth,1,2 Anikó Papp,1 Anna Szűcs,1 1Department of Neurology, National Institute of Clinical Neurosciences, 2János Szentágothai Doctoral School of Neurosciences, Semmelweis University School of PhD Studies, Budapest, Hungary Abstract: Nonrapid eye movement (NREM) or arousal parasomnias are prevalent conditions in children and young adults, apparently provoked by any medical, physical, mental, or pharmacologic/toxic agent disturbing normal biorhythm and causing sleep fragmentation or abundant amount of slow wave sleep. The nadir and the ascending slope of the first sleep cycle of night sleep are the typical periods when NREM parasomnias, especially sleepwalking may occur on sleep-microstructural level; microarousals are the typical moments allowing NREM parasomnias. While sleep-disturbing factors have a clear precipitating effect, a genetic predisposition appears necessary in most cases. A candidate gene for sleepwalking has been identified on chromosome 20q12-q13.12 in one sleepwalking family. NREM parasomnias have a genetic and clinical link with nocturnal-frontal lobe epilepsies; possibly through an abnormality of the acetylcholine-related sleep-control system. The association of NREM parasomnias with the human leukocyte antigen system might be the sign of an autoimmune background to be further clarified. In the treatment of arousal parasomnias, the main tools are adequate sleep hygiene and the management of underlying conditions. Their pharmacotherapy has remained unresolved; the best options are clonazepam and some of the antidepressants, while a psychotherapy approach is also justified. Keywords: sleep disorders, arousal disorders, NREM parasomnia, sleepwalking, sleep terror
format article
author Horváth A
Papp A
Szűcs A
author_facet Horváth A
Papp A
Szűcs A
author_sort Horváth A
title Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
title_short Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
title_full Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
title_fullStr Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
title_full_unstemmed Progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
title_sort progress in elucidating the pathophysiological basis of nonrapid eye movement parasomnias: not yet informing therapeutic strategies
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/658d3f50ed5b41628f8ffc398a65b575
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