ArticleScientific reports2025
Exploring differences in signaling pathways of the circadian clock and neuromodulators in obstructive sleep apnea.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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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.
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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.
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Who cites it
6 citing papers in PubMed.
- Molecular Drivers of Cognitive Decline and Neuroprotection in Obstructive Sleep Apnea: A Narrative Review.Antioxidants (Basel, Switzerland) · 2026Review
- BDNF Haploinsufficiency Limits Voluntary Exercise-Induced Adult Hippocampal Neurogenesis.Biology · 2026Article
- Review
- Associations Between Sleep Deprivation, Circadian Gene Expression, Depressive Symptoms, and Psychomotor Performance-Preliminary Results.Journal of clinical medicine · 2026Article
- The vicious cycle of circadian disruption and obstructive sleep apnea: implications for cancer risk.Journal of the National Cancer Center · 2026Article
- Circadian Blood Pressure Phenotyping Identifies Subtype-Specific Risk and Outcomes in Acute Ischemic Stroke: A Prospective Study.Translational stroke research · 2025Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Obstructive sleep apnea (OSA) is a prevalent disorder characterized by recurring upper airway obstructions, leading to disrupted sleep and systemic complications. The complexity of OSA suggests intricate interactions between neuromodulators and circadian clock genes. This study aimed to explore the expression levels of circadian rhythm genes and neurotrophins (NTs) in OSA patients compared to controls. Participants (166 OSA patients, 64 controls) were enrolled. Blood samples collected post-polysomnography (PSG), underwent RNA extraction from peripheral blood lymphocytes and RT-PCR was performed for gene expression analysis. In the OSA group, the expression of BMAL1, CLOCK, CRY1, PER1, NPAS2, NR1D1, and HIF-1β was positively correlated with BDNF expression (p < 0.05 for all). Conversely, in the control group, only PER1 mRNA showed a correlation with BDNF expression (R = 0.280, p = 0.017). NF-κβ expression demonstrated a positive correlation with BMAL1, CLOCK, CRY1, PER1, NPAS2, NR1D1, HIF-1α, and HIF-1β expressions in both groups (p < 0.05 for all). HIF-1α and HIF1-β mRNA expressions were positively correlated with BMAL1, CLOCK, CRY1, PER1, NPAS2, and NR1D1 expressions regardless of the presence of OSA (p < 0.05 for all). The study underscores the intricate interactions among circadian rhythm genes, NTs, and transcription factors in OSA, providing a basis for potential targeted therapeutic interventions.
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