AUTHOR=Jing Mei , Guo Min , Wang Xinrui , Zhang Peng , Gu Chenchen , Zhang Nan , Ding Zhiqiang , Su Kelei 

TITLE=Changes of regional brain activity in frontal areas associated with cognitive impairment in obstructive sleep apnea-hypopnea syndrome patients: a resting-state fMRI study

JOURNAL=Frontiers in Neuroscience

VOLUME=Volume 19 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2025.1587180

DOI=10.3389/fnins.2025.1587180

ISSN=1662-453X

ABSTRACT=IntroductionObstructive sleep apnea-hypopnea syndrome (OSAHS) can lead to cognitive impairment, however, its central neural mechanism is still unclear.MethodsResting-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.ResultsOSAHS 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.ConclusionSevere 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.