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Aberrant network topology of cortical-subcortical circuits in schizophrenia and bipolar disorder: a graph theory study

Aug 2026 · Frontiers in Psychiatry · Vol 17 · 0 citations · 73 references
Medicine

TL;DR

These results revealed global-level network abnormalities in both SCH and BD, with more extensive nodal- and module-level abnormalities in SCH, which could be useful biomarkers for differential diagnosis as well as treatment guidance and response evaluation.

Abstract

Background Schizophrenia (SCH) or bipolar disorder (BD) patients exhibit a variety of abnormalities in brain network organization and function. More comprehensive characterization of both shared and disease-specific network features could provide essential clues to the underlying pathogenesis of these disorders, as well as potential therapeutic targets. Objective In this study, we used graph theory methods to examine the common and specific characteristics of brain network between schizophrenia and bipolar disorder. Method The patients of schizophrenia (n = 89) , patients of bipolar disorder (n = 57) and healthy control (HC) subjects (n = 45) were recruited. Resting-state functional magnetic resonance images were analyzed with a group-level connectivity matrix (GCM) threshold varying from 0.10 to 0.40 in 0.02 steps. Results Network synchronization at the global level was significantly reduced in both SCH and BD groups compared to the HC group. Patients also exhibited impaired nodal parameters (nodal degree and betweenness centrality), especially SCH patients, in the hippocampus, temporal lobe, parietal lobe, and occipital lobe. The SCH group demonstrated sparser edges [fewer functional connectivity (FC) pathways] within somatosensory-motor Module I, denser edges (stronger FC) within limbic Module V, and reduced edge density between Module I and Module IV (including the default mode network), while both SCH and BD patients displayed denser edges between attention control Module III and Module V. Conclusions These results revealed global-level network abnormalities in both SCH and BD, with more extensive nodal- and module-level abnormalities in SCH. These distinct topological characteristics could be useful biomarkers for differential diagnosis as well as treatment guidance and response evaluation.

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