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Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice

Sleep problems have not been directly reported in phenylketonuria (PKU). In PKU, the metabolic pathway of phenylalanine is disrupted, which, among others, causes deficits in the neurotransmitters and sleep modulators dopamine, norepinephrine, and serotonin. Understanding sleep problems in PKU patien...

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Autores principales: Bruinenberg, Vibeke M., Gordijn, Marijke C. M., MacDonald, Anita, van Spronsen, Francjan J., Van der Zee, Eddy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405067/
https://www.ncbi.nlm.nih.gov/pubmed/28491049
http://dx.doi.org/10.3389/fneur.2017.00167
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author Bruinenberg, Vibeke M.
Gordijn, Marijke C. M.
MacDonald, Anita
van Spronsen, Francjan J.
Van der Zee, Eddy A.
author_facet Bruinenberg, Vibeke M.
Gordijn, Marijke C. M.
MacDonald, Anita
van Spronsen, Francjan J.
Van der Zee, Eddy A.
author_sort Bruinenberg, Vibeke M.
collection PubMed
description Sleep problems have not been directly reported in phenylketonuria (PKU). In PKU, the metabolic pathway of phenylalanine is disrupted, which, among others, causes deficits in the neurotransmitters and sleep modulators dopamine, norepinephrine, and serotonin. Understanding sleep problems in PKU patients may help explain the pathophysiology of brain dysfunction in PKU patients. In this explorative study, we investigated possible sleep problems in adult treated PKU patients and untreated PKU mice. In the PKU patients, sleep characteristics were compared to healthy first degree relatives by assessment of sleep disturbances, sleep–wake patterns, and sleepiness with the help of four questionnaires: Holland sleep disorder questionnaire, Pittsburgh sleep quality index, Epworth sleepiness scale, and Munich Chronotype Questionnaire. The results obtained with the questionnaires show that PKU individuals suffer more from sleep disorders, a reduced sleep quality, and an increased latency to fall asleep and experience more sleepiness during the day. In the PKU mice, activity patterns were recorded with passive infrared recorders. PKU mice switched more often between active and non-active behavior and shifted a part of their resting behavior into the active period, confirming that sleep quality is affected as a consequence of PKU. Together, these results give the first indication that sleep problems are present in PKU. More detailed future research will give a better understanding of these problems, which could ultimately result in the improvement of treatment strategies by including sleep quality as an additional treatment target.
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spelling pubmed-54050672017-05-10 Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice Bruinenberg, Vibeke M. Gordijn, Marijke C. M. MacDonald, Anita van Spronsen, Francjan J. Van der Zee, Eddy A. Front Neurol Neuroscience Sleep problems have not been directly reported in phenylketonuria (PKU). In PKU, the metabolic pathway of phenylalanine is disrupted, which, among others, causes deficits in the neurotransmitters and sleep modulators dopamine, norepinephrine, and serotonin. Understanding sleep problems in PKU patients may help explain the pathophysiology of brain dysfunction in PKU patients. In this explorative study, we investigated possible sleep problems in adult treated PKU patients and untreated PKU mice. In the PKU patients, sleep characteristics were compared to healthy first degree relatives by assessment of sleep disturbances, sleep–wake patterns, and sleepiness with the help of four questionnaires: Holland sleep disorder questionnaire, Pittsburgh sleep quality index, Epworth sleepiness scale, and Munich Chronotype Questionnaire. The results obtained with the questionnaires show that PKU individuals suffer more from sleep disorders, a reduced sleep quality, and an increased latency to fall asleep and experience more sleepiness during the day. In the PKU mice, activity patterns were recorded with passive infrared recorders. PKU mice switched more often between active and non-active behavior and shifted a part of their resting behavior into the active period, confirming that sleep quality is affected as a consequence of PKU. Together, these results give the first indication that sleep problems are present in PKU. More detailed future research will give a better understanding of these problems, which could ultimately result in the improvement of treatment strategies by including sleep quality as an additional treatment target. Frontiers Media S.A. 2017-04-26 /pmc/articles/PMC5405067/ /pubmed/28491049 http://dx.doi.org/10.3389/fneur.2017.00167 Text en Copyright © 2017 Bruinenberg, Gordijn, MacDonald, van Spronsen and Van der Zee. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Bruinenberg, Vibeke M.
Gordijn, Marijke C. M.
MacDonald, Anita
van Spronsen, Francjan J.
Van der Zee, Eddy A.
Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title_full Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title_fullStr Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title_full_unstemmed Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title_short Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice
title_sort sleep disturbances in phenylketonuria: an explorative study in men and mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405067/
https://www.ncbi.nlm.nih.gov/pubmed/28491049
http://dx.doi.org/10.3389/fneur.2017.00167
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