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Altered Neurovascular Coupling in Obstructive Sleep Apnoea: Assessment via CBF-ALFF Spatial Coupling.

Created on 09 Oct 2026

Authors

Hong Liu, Xin Huang, Shusheng Gong, Lu Lu, Zhenchang Wang, Xiaoshuai Li, Bin Liu

Published in

The British journal of radiology. Oct 09, 2026. Epub Oct 09, 2026.

Abstract

To investigate alterations in CBF-ALFF spatial coupling in obstructive sleep apnoea (OSA).
Thirty-two patients with OSA and 32 healthy controls(HCs) matched for sex, age, and education background were recruited for this work. All participants received arterial spin labelling (ASL) and resting-state functional MRI (rs-fMRI) examinations. Cerebral blood flow (CBF) and amplitude of low-frequency fluctuation (ALFF) maps were derived from ASL and fMRI data, respectively. Between-group comparisons were performed to identify differences in ALFF, CBF, and CBF-ALFF coupling metrics. Subsequently, correlation analyses were conducted in OSA patients to investigate whether CBF/ALFF ratios derived from brain regions exhibiting significant group-level differences were associated with polysomnographic and clinical parameters.
Patients with OSA exhibited reduced global spatial CBF-ALFF coupling relative to HCs. Regionally, decreased CBF/ALFF ratios were primarily observed in the left parahippocampal gyrus, whereas increased ratios were located mainly in the default mode network (DMN), including the left precuneus, right angular gyrus, and left inferior parietal lobule.
This study demonstrated disrupted spatial CBF-ALFF coupling in OSA patients. Such coupling alterations reflect broad OSA-associated pathophysiological changes, including but not limited to neurovascular dysfunction, offering new insights into the neuropathological mechanisms of OSA.
Using combined BOLD and ASL imaging, this study provides the first characterization of both global and regional CBF-ALFF coupling alterations in OSA, revealing distinct uncoupling signatures in the DMN and medial temporal lobe that deepen our understanding of OSA-related neurovascular pathophysiology.

PMID:
42853094
Bibliographic data and abstract were imported from PubMed on 09 Oct 2026.

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