Abstract

BackgroundThe function, cytoarchitecture and connectivity of the insula cortex are diverse. Cluster analyses have been applied to functional magnetic resonance imaging (MRI) connectivity data to parse this diversity and subdivide the insula into discrete subregions. However, the number of subregions comprising the insula remains vexed and whether these putative subregions are disturbed in neuropsychiatric illness are unknown. The present study aimed to (i) rigorously evaluate the number of subregions (if any) into which the insula can be subdivided based on topographic variation in whole-brain patterns of insula functional connectivity; and, (ii) establish whether the connectional topography of the insula is altered in schizophrenia.MethodsTwo alternative models explaining the heterogeneity of insula connectivity were tested: (Model i) insula comprising discrete subregions, each associated with a distinct connectivity fingerprint; and, (Model ii) connectivity varying as a continuum across insula, without marked boundaries. Cluster analysis was used to delineate discrete subregions, and a novel gradient-based method was developed to evaluate whether connectivity varied continuously across the insula. These models were tested in a sample of individuals with schizophrenia (N=49), healthy comparison individuals (N=52) and an independent validation cohort from the Human Connectome Project (N=50).ResultsCluster analyses indicated that the insula comprised anterior and posterior subregions, with significantly less differentiation in connectivity patterns between these two clusters in the schizophrenia group (right: P=.0038; left: P=.002). The anterior insula was more strongly connected to the sensory-motor, occipital/parietal cortex and posterior lobe of cerebellum in the schizophrenia group, whereas the connectivity between the posterior insula and prefrontal cortex and thalamus was stronger in the patients (PFWE<.05). The dysconnectivity between anterior insula and anterior cingulate cortex was correlated with the severity of emotion withdrawal (Jonckeere-Terpstra test; JT=-3.74, P<.001). Most importantly however, for the majority of individuals in both datasets, the degree of cluster separation between insula subregions identified with cluster analyses was not significantly improved compared to clusters delineated in null data that was generated from white matter, where no clusters were expected. Modeling patterns of insula connectivity as continua of variation across a rostrocaudal axis was found to provide a more parsimonious model than using distinct subregions segregated by sharp boundaries. The variation in connectivity across this rostrocaudal axis was significantly reduced in schizophrenia patients (P=0.02).DiscussionThis is the first study that comprehensively investigate the potential differences in connectional pathology of insula between its anterior and posterior aspects. We conclude that the connectional diversity of the insula inferred from resting-state functional connectivity should be conceptualized as continua of variation, rather than discrete subregions. We posit that the reduced differentiation between the anterior and posterior insula in schizophrenia may impact on the ability in discriminating self-generated from externally-generated sensory information, possibly contributing to hallucinations in the disorder.

Highlights

  • The function, cytoarchitecture and connectivity of the insula cortex are diverse

  • Two alternative models explaining the heterogeneity of insula connectivity were tested: (Model i) insula comprising discrete subregions, each associated with a distinct connectivity fingerprint; and, (Model ii) connectivity varying as a continuum across insula, without marked boundaries

  • The current study aims to explore the 40 Hz auditory steady state responses (ASSR) in first-episode of psychosis patients and individuals at clinical high risk (CHR) of psychosis, and the possible relationship of deficits in gamma-band entrainment to a dysfunctional excitation inhibition balance, as reflected by alterations in cortical GABA and glutamate

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Summary

Results

We find strong correlations of EEG with both PEs in both samples: lower-level PEs show effects early on (Study1: 133ms post-stimulus, Study2: 177ms), higher-level PEs later (Study1: 240ms, Study2: 450ms). The temporal order of these signatures mimics the hierarchical relationship of the PEs, as proposed by our computational model, where lower level beliefs need to be updated before learning can ensue on higher levels. Ketamine significantly reduced the representation of the higher-level PE in Study. (Study has not been unblinded.) Discussion: These studies present first evidence for hierarchical PEs during MMN and demonstrate that single-trial analyses guided by a computational model can distinguish different types (levels) of PEs, which are differentially linked to neuromodulators of demonstrated relevance for schizophrenia. Our analysis approach provides better mechanistic interpretability of pharmacological MMN studies, which will hopefully support the development of computational assays for diagnosis and treatment predictions in schizophrenia. Ye Tian*,1, Chad Bousman, Chenxing Liu, Christos Pantelis, Andrew Zalesky3 1The University of Melbourne; 2University of Calgary; 3The University of Melbourne, Melbourne Neuropsychiatry Centre

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