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Chronic upregulation of circadian clock protein per1 among OSA patients
INTRODUCTION: PER1 is a repressor protein involved in regulating circadian rhythm. While obstructive sleep apnea (OSA) is characterized by recurred pauses in breathing caused by the collapse of the upper airways it might be associated with disruption of the circadian clock. OBJECTIVES: The study aim...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476071/ http://dx.doi.org/10.1192/j.eurpsy.2021.1479 |
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author | Gabryelska, A. Sochal, M. Bialasiewicz, P. |
author_facet | Gabryelska, A. Sochal, M. Bialasiewicz, P. |
author_sort | Gabryelska, A. |
collection | PubMed |
description | INTRODUCTION: PER1 is a repressor protein involved in regulating circadian rhythm. While obstructive sleep apnea (OSA) is characterized by recurred pauses in breathing caused by the collapse of the upper airways it might be associated with disruption of the circadian clock. OBJECTIVES: The study aimed to assess PER1 protein in OSA patients and evaluate its association with PSG parameters. METHODS: The study included 40 individuals, who underwent diagnostic polysomnography (PSG) examination. Based apnea-hypopnea index (AHI) patients were divided into groups: control (AHI<5; n=10) and OSA (AHI5; n=30). All participants had their peripheral blood collected in the evening (9:00-10:00 pm) before and in the morning (6:00-7:00 am) after the PSG. PER1 protein concertation measurements were performed using ELISA. Funding: National Science Centre, Poland-2018/31/N/NZ5/03931. RESULTS: The control and OSA group were match in sex and age, while differed regarding BMI (p=0.039), desaturation index (p<0.001) and AHI (p<0.001). PER1 protein level was elevated in OSA group compared to control both in the evening (322.384.1vs.208.460.1pg/ml;p<0.001) and morning (314.891.9vs.228.157.3pg/ml;p=0.002). No difference was observed between evening and morning PER1 level (p=0.946). Morning PER1 correlated with AHI (r=0.400; p=0.011), desaturation index (r=0.391;p=0.013), age (r=-0.312;p=0.049) and BMI (r=0.383;p=0.015). In a multiple linear regression model (R(2)=0.268;p=0.003) morning PER1 protein level was influenced by age (p=0.006) and AHI (p=0.025), while BMI and desaturation index were not significant. CONCLUSIONS: OSA patients might suffer from circadian clock disruption, which is mainly associated with the severity of the disorder and age. Further studies are needed as this dysregulation can result in metabolic and mood disorders often observed in this group of patients. |
format | Online Article Text |
id | pubmed-9476071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94760712022-09-29 Chronic upregulation of circadian clock protein per1 among OSA patients Gabryelska, A. Sochal, M. Bialasiewicz, P. Eur Psychiatry Abstract INTRODUCTION: PER1 is a repressor protein involved in regulating circadian rhythm. While obstructive sleep apnea (OSA) is characterized by recurred pauses in breathing caused by the collapse of the upper airways it might be associated with disruption of the circadian clock. OBJECTIVES: The study aimed to assess PER1 protein in OSA patients and evaluate its association with PSG parameters. METHODS: The study included 40 individuals, who underwent diagnostic polysomnography (PSG) examination. Based apnea-hypopnea index (AHI) patients were divided into groups: control (AHI<5; n=10) and OSA (AHI5; n=30). All participants had their peripheral blood collected in the evening (9:00-10:00 pm) before and in the morning (6:00-7:00 am) after the PSG. PER1 protein concertation measurements were performed using ELISA. Funding: National Science Centre, Poland-2018/31/N/NZ5/03931. RESULTS: The control and OSA group were match in sex and age, while differed regarding BMI (p=0.039), desaturation index (p<0.001) and AHI (p<0.001). PER1 protein level was elevated in OSA group compared to control both in the evening (322.384.1vs.208.460.1pg/ml;p<0.001) and morning (314.891.9vs.228.157.3pg/ml;p=0.002). No difference was observed between evening and morning PER1 level (p=0.946). Morning PER1 correlated with AHI (r=0.400; p=0.011), desaturation index (r=0.391;p=0.013), age (r=-0.312;p=0.049) and BMI (r=0.383;p=0.015). In a multiple linear regression model (R(2)=0.268;p=0.003) morning PER1 protein level was influenced by age (p=0.006) and AHI (p=0.025), while BMI and desaturation index were not significant. CONCLUSIONS: OSA patients might suffer from circadian clock disruption, which is mainly associated with the severity of the disorder and age. Further studies are needed as this dysregulation can result in metabolic and mood disorders often observed in this group of patients. Cambridge University Press 2021-08-13 /pmc/articles/PMC9476071/ http://dx.doi.org/10.1192/j.eurpsy.2021.1479 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Gabryelska, A. Sochal, M. Bialasiewicz, P. Chronic upregulation of circadian clock protein per1 among OSA patients |
title | Chronic upregulation of circadian clock protein per1 among OSA patients |
title_full | Chronic upregulation of circadian clock protein per1 among OSA patients |
title_fullStr | Chronic upregulation of circadian clock protein per1 among OSA patients |
title_full_unstemmed | Chronic upregulation of circadian clock protein per1 among OSA patients |
title_short | Chronic upregulation of circadian clock protein per1 among OSA patients |
title_sort | chronic upregulation of circadian clock protein per1 among osa patients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476071/ http://dx.doi.org/10.1192/j.eurpsy.2021.1479 |
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