ArticleFrontiers in neuroscience2025
Changes of regional brain activity in frontal areas associated with cognitive impairment in obstructive sleep apnea-hypopnea syndrome patients: a resting-state fMRI study.
Article in Frontiers in neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Arterial Hypertension as a Modulator of Cognitive Response to CPAP Therapy in Moderate-to-Severe Obstructive Sleep Apnea.Medicina (Kaunas, Lithuania) · 2026Article
- Neurocognitive Recovery Following Continuous Positive Airway Pressure Therapy in Patients with Moderate to Severe Obstructive Sleep Apnea.Journal of clinical medicine · 2025Article
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Authors and funding
8 authors.
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Abstract
Introduction: Obstructive sleep apnea-hypopnea syndrome (OSAHS) can lead to cognitive impairment, however, its central neural mechanism is still unclear. Methods: Resting-state functional magnetic resonance imaging (rs-fMRI) data were collected from 31 severe OSAHS patients and 28 healthy controls (HCs). Both regional homogeneity (ReHo) and fractional amplitude of low-frequency fluctuation (fALFF) measures were calculated and compared between groups. Moreover, the correlations between abnormal regions and Montreal Cognitive Assessment (MoCA) scores were evaluated using Pearson correlation analysis. Finally, ROC analysis was performed to evaluate the values of abnormal brain regions for distinguishing OSAHS patients from HCs. Results: OSAHS patients had decreased MoCA scores when compared with HCs. In comparison with HCs, increased ReHo values were found in the left and right rolandic operculum of OSAHS patients. In addition, decreased fALFF values were identified in the right superior frontal gyrus, right postcentral gyrus, left angular gyrus while increased fALFF values were identified in the left thalamus, right thalamus and right putamen of OSAHS patients. Positive relationships were found between fALFF values of the right superior frontal gyrus and MoCA scores in the patient group. The results of ROC analysis showed that the combined model of (ReHo and fALFF values of all abnormal brain regions) could effectively distinguish OSAHS from HCs. Conclusion: Severe OSAHS patients showed decreased brain activities, which were associated with the decreased cognition of patients. In addition, abnormal brain regions could help distinguishing OSAHS patients from HCs. These findings provided new insights about the potential pathogenesis of cognitive impairment caused by OSAHS from the perspective of changes in brain activity.
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