Evidence map›Paper›PMID 39375341›Full record

ArticleTranslational psychiatry2024

Circadian clock dysregulation: a potential mechanism of depression in obstructive sleep apnea patients.

Agata Gabryelska, Szymon Turkiewicz, Piotr Kaczmarski, Adrian Gajewski, Piotr Białasiewicz, Dominik Strzelecki, Maciej Chałubiński, Marcin Sochal

Abstract read
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Agata GabryelskaDepartment of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, Lodz, Poland. agata.gabryelska@gmail.com.ORCID 0000-0002-4430-6488
Szymon TurkiewiczDepartment of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, Lodz, Poland.ORCID 0000-0001-6399-8742
Piotr KaczmarskiDepartment of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, Lodz, Poland.ORCID 0000-0001-6875-7024
Adrian GajewskiDepartment of Immunology and Allergy, Medical University of Lodz, Lodz, Poland.
Piotr BiałasiewiczDepartment of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, Lodz, Poland.
Dominik StrzeleckiDepartment of Affective and Psychotic Disorders, Medical University of Lodz, Lodz, Poland.
Maciej ChałubińskiDepartment of Immunology and Allergy, Medical University of Lodz, Lodz, Poland.
Marcin SochalDepartment of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, Lodz, Poland.

Funding

Narodowe Centrum Nauki (National Science Centre) 2018/31/N/NZ5/03931
6 · The paper itself

Abstract

Obstructive sleep apnea (OSA) is characterized by co-occurrence with affective disorders. Our study aims to investigate the association of circadian clock gene expressions, and the presence and severity of depressive symptoms in OSA patients. The study included 184 individuals, who underwent polysomnography (PSG) and had their peripheral blood collected in the evening before and the morning after the PSG. Patients were divided into two groups: the OSA (apnea-hypopnea index (AHI) > 5) and the control group (AHI < 5). RNA was extracted from peripheral blood leukocytes. Expression levels of the selected genes (BMAL1, CLOCK, PER1, CRY1, NPAS2, and NR1D1) were assessed by qRT-PCR. Questionnaire data was collected in the morning (including the Insomnia Severity Index (ISI), Epworth Sleepiness Scale (ESS), Chronotype Questionnaire (CQ), and Montgomery-Åsberg Depression Rating Scale (MADRS)). The expression of all examined circadian clock genes in OSA patients was upregulated in the morning compared to the evening (except NPAS2). No differences were observed between OSA and control groups at either time point. Additionally, there was a positive correlation between the severity of depressive symptoms (assessed with MADRS) and morning expression of circadian genes in the group of OSA patients. Finally, in multivariable linear regression, ISI score (B = 0.750, p < 0.001), AM score of CQ (B = 0.416, p = 0.007), and morning PER1 gene expression (B = 4.310, p = 0.042) were found to be predictive factors for greater severity of depression symptoms in OSA patients. Dysregulated circadian clock gene expression in OSA patients is linked to depressive symptom severity, suggesting circadian disruption may underlie affective symptoms in OSA.

Indexed as

Circadian ClocksDepressionPolysomnographySleep Apnea, ObstructiveAdultARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsCircadian RhythmCLOCK ProteinsCryptochromesFemaleHumansMaleMiddle AgedNerve Tissue ProteinsSeverity of Illness IndexARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsBMAL1 protein, humanCLOCK protein, humanCLOCK ProteinsCRY1 protein, humanCryptochromesNerve Tissue ProteinsNPAS2 protein, human

Identifiers

PMID39375341
PMCPMC11458778

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.