Investigating the Link between Circadian Clock Gene Expressions, Chronotype, Insomnia, and Daytime Sleepiness in Patients with Obstructive Sleep Apnea.
Humans
Male
Sleep Initiation and Maintenance Disorders
/ genetics
Female
Sleep Apnea, Obstructive
/ genetics
Middle Aged
Circadian Clocks
/ genetics
Adult
Circadian Rhythm
/ genetics
Polysomnography
ARNTL Transcription Factors
/ genetics
CLOCK Proteins
/ genetics
Gene Expression Regulation
Sleepiness
Surveys and Questionnaires
Chronotype
Cryptochromes
OSA
chronotype
circadian clock
genes
insomnia
sleep medicine
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
21 Aug 2024
21 Aug 2024
Historique:
received:
13
07
2024
revised:
16
08
2024
accepted:
19
08
2024
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
29
8
2024
Statut:
epublish
Résumé
This study aimed to investigate the relationship between obstructive sleep apnea (OSA), circadian rhythms, and individual sleep-wake preferences, as measured by chronotype, and to assess the association between circadian clock gene expression and subjective sleep-related variables. A total of 184 individuals were recruited, underwent polysomnography (PSG), and completed questionnaires including a chronotype questionnaire (CQ), insomnia severity index (ISI), and Epworth sleepiness scale (ESS). Blood samples were collected in the evening before and morning after PSG. Gene expression analysis included BMAL1, CLOCK, PER1, CRY1, NPAS2, and NR1D1. In the OSA group, the subjective amplitude (AM score of CQ) positively correlated with all circadian clock genes in the morning (R ≥ 0.230 and The findings highlight the complex interplay between OSA, circadian rhythms, and sleep-related variables, suggesting potential determinants of morning chronotype in OSA and implicating disrupted circadian clock function in subjective feelings of energy throughout the day. Further research is warranted to elucidate underlying mechanisms and guide personalized management strategies.
Identifiants
pubmed: 39201748
pii: ijms25169062
doi: 10.3390/ijms25169062
pii:
doi:
Substances chimiques
ARNTL Transcription Factors
0
CLOCK Proteins
EC 2.3.1.48
BMAL1 protein, human
0
CRY1 protein, human
0
Cryptochromes
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Science Centre, Poland
ID : 2018/31/N/NZ5/03931