Authors
Liang Gong, Duan Liu, Bei Zhang, Haoyu Li, Yuan He, Ronghua Xu, Wenjun Zhou, Chunhua Xi
Published in
Brain and behavior. Volume 16. Issue 10. Pages e71830.
Abstract
Chronic insomnia disorder (CID) is highly comorbid with depression and anxiety, yet the neurostructural basis of this affective comorbidity remains unclear. This study aimed to investigate individualized structural covariance network (iSCN) alterations in CID and their associations with depressive and anxiety symptoms using a novel dynamic time warping (DTW) approach.
A total of 257 CID patients and 247 good sleep controls (GSCs) underwent T1-weighted structural magnetic resonance imaging. Individualized SCNs were constructed based on gray matter volume using the DTW algorithm to quantify interregional morphological similarity. Graph theory analysis was applied to assess global and nodal network topological properties. Clinical symptoms were evaluated using standardized scales (PSQI, SDS, SAS). FINDINGS: Compared with GSCs, patients with CID exhibited significant disruptions in global network topology, including reduced local efficiency, global efficiency, and small-world properties (Gamma and Sigma). At the nodal level, both increased and decreased nodal degree and betweenness centrality were observed in regions involved in emotion regulation, arousal, and sensory processing, including the orbitofrontal cortex, amygdala, thalamus, and caudate nucleus. These nodal metrics were significantly associated with depressive and anxiety symptom severity after correction for multiple comparisons.
Our findings demonstrate that CID is characterized by disrupted iSCN organization, and that nodal alterations within emotion-, arousal-, and sensory-related regions are associated with the severity of depressive and anxiety symptoms. These findings identify altered large-scale structural coordination as a neural correlate of affective symptom burden in CID.
PMID:
42885342
Bibliographic data and abstract were imported from PubMed on 16 Oct 2026.
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