Developmental Trajectories of Cortical Thickness in Relation to Schizotypy During Adolescence.

Investigating potential gray matter differences in adolescents presenting higher levels of schizotypy personality traits could bring further insights into the development of schizophrenia spectrum disorders. Research has yet to examine the morphological correlates of schizotypy features during adolescence prospectively, and no information is available on the developmental trajectories from adolescence to adulthood. We employed mixed model regression analysis to investigate developmental trajectories of cortical thickness (CT) in relation to schizotypy dimensions in a cohort of 109 adolescents from the general population for whom MRI-scans were acquired over a 5-year period, culminating in a total of 271 scans. Structural data were processed with FreeSurfer software, statistical analyses were conducted using mixed regression models following a ROI-based approach, and schizotypy was assessed with the Schizotypal Personality Questionnaire (SPQ). Accelerated thinning was observed in the posterior cingulate cortex in relation to high levels of positive schizotypy, whereas high levels of disorganized schizotypy were associated with a similar trajectory pattern in the anterior cingulate cortex. The developmental course of CT in the prefrontal, occipital, and cingulate cortices differed between adolescents expressing higher vs lower levels of negative schizotypy. Participants reporting high scores on all schizotypy dimensions were associated with differential trajectories of CT in posterior cingulate cortex and occipital cortex. Consistently with prospective developmental studies of clinical risk conversion, the negative schizotypy dimension appears to constitute the most informative dimension for psychosis-related psychopathology, as its cerebral correlates in adolescents most closely overlap with results found in clinical high risk for psychosis studies.

[1]  S. Eliez,et al.  Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS , 2019, Molecular Psychiatry.

[2]  Tyrone D. Cannon,et al.  Cortical abnormalities in youth at clinical high-risk for psychosis: Findings from the NAPLS2 cohort , 2019, NeuroImage: Clinical.

[3]  Matthijs Vink,et al.  Symptom attribution and frontal cortical thickness in first‐episode schizophrenia , 2018, Early intervention in psychiatry.

[4]  A. Egerton,et al.  Neuroanatomical changes in people with high schizotypy: relationship to glutamate levels , 2017, Psychological Medicine.

[5]  S. Blakemore,et al.  Development of the Cerebral Cortex across Adolescence: A Multisample Study of Inter-Related Longitudinal Changes in Cortical Volume, Surface Area, and Thickness , 2017, The Journal of Neuroscience.

[6]  S. Eliez,et al.  Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome , 2016, European Psychiatry.

[7]  David W. Evans,et al.  Neural substrates of a schizotypal spectrum in typically-developing children: Further evidence of a normal-pathological continuum , 2016, Behavioural Brain Research.

[8]  D. Hubl,et al.  Psychosis-predictive value of self-reported schizotypy in a clinical high-risk sample. , 2016, Journal of abnormal psychology.

[9]  K. Waldie,et al.  Identifying grey matter changes in schizotypy using partial least squares correlation , 2016, Cortex.

[10]  Murat Yücel,et al.  Brain development during adolescence: A mixed‐longitudinal investigation of cortical thickness, surface area, and volume , 2016, Human brain mapping.

[11]  J. Rapoport,et al.  Severity of Cortical Thinning Correlates With Schizophrenia Spectrum Symptoms. , 2016, Journal of the American Academy of Child and Adolescent Psychiatry.

[12]  Wen-hua Liu,et al.  The neural basis of olfactory function and its relationship with anhedonia in individuals with schizotypy: An exploratory study , 2015, Psychiatry Research: Neuroimaging.

[13]  Eve C. Johnstone,et al.  Grey matter networks in people at increased familial risk for schizophrenia , 2015, Schizophrenia Research.

[14]  Christian Gaser,et al.  Brain structural correlates of schizotypy and psychosis proneness in a non-clinical healthy volunteer sample , 2015, Schizophrenia Research.

[15]  S. Lawrie,et al.  Cortical Surface Area Differentiates Familial High Risk Individuals Who Go on to Develop Schizophrenia , 2015, Biological Psychiatry.

[16]  S. Eliez,et al.  Developing psychosis and its risk states through the lens of schizotypy. , 2015, Schizophrenia bulletin.

[17]  D. Yin,et al.  Neurobiological changes of schizotypy: evidence from both volume-based morphometric analysis and resting-state functional connectivity. , 2015, Schizophrenia bulletin.

[18]  Christina J. Herold,et al.  Comparison of grey matter volume and thickness for analysing cortical changes in chronic schizophrenia: A matter of surface area, grey/white matter intensity contrast, and curvature , 2015, Psychiatry Research: Neuroimaging.

[19]  Tyrone D. Cannon,et al.  Progressive Reduction in Cortical Thickness as Psychosis Develops: A Multisite Longitudinal Neuroimaging Study of Youth at Elevated Clinical Risk , 2015, Biological Psychiatry.

[20]  P. DeRosse,et al.  Evidence from structural and diffusion tensor imaging for frontotemporal deficits in psychometric schizotypy. , 2015, Schizophrenia bulletin.

[21]  J. Muñiz,et al.  Schizotypal Personality Questionnaire: New sources of validity evidence in college students , 2014, Psychiatry Research.

[22]  R. Kahn,et al.  Cortical thickness in individuals with non-clinical and clinical psychotic symptoms. , 2014, Brain : a journal of neurology.

[23]  N. Koutsouleris,et al.  Genetics, Cognition, and Neurobiology of Schizotypal Personality: A Review of the Overlap with Schizophrenia , 2013, Front. Psychiatry.

[24]  Eve C. Johnstone,et al.  Cortical thickness in first-episode schizophrenia patients and individuals at high familial risk: A cross-sectional comparison , 2013, Schizophrenia Research.

[25]  Stephan Eliez,et al.  Sex differences in thickness, and folding developments throughout the cortex , 2013, NeuroImage.

[26]  D. Prvulovic,et al.  Association between psychotic symptoms and cortical thickness reduction across the schizophrenia spectrum. , 2013, Cerebral cortex.

[27]  Ying Lu,et al.  Model selection in linear mixed effect models , 2012, J. Multivar. Anal..

[28]  Bruce Fischl,et al.  Within-subject template estimation for unbiased longitudinal image analysis , 2012, NeuroImage.

[29]  R. Kahn,et al.  Progressive structural brain changes during development of psychosis. , 2012, Schizophrenia bulletin.

[30]  Bruce Fischl,et al.  Avoiding asymmetry-induced bias in longitudinal image processing , 2011, NeuroImage.

[31]  A. Mechelli,et al.  Neuroanatomical abnormalities that predate the onset of psychosis: a multicenter study. , 2011, Archives of general psychiatry.

[32]  Bruce Fischl,et al.  Highly accurate inverse consistent registration: A robust approach , 2010, NeuroImage.

[33]  Arthur W. Toga,et al.  The contributions of disease and genetic factors towards regional cortical thinning in schizophrenia: The UCLA family study , 2010, Schizophrenia Research.

[34]  N. Andreasen,et al.  Global and regional cortical thinning in first-episode psychosis patients: relationships with clinical and cognitive features , 2010, Psychological Medicine.

[35]  Anders M. Dale,et al.  CORTICAL THICKNESS AND SUBCORTICAL VOLUMES IN SCHIZOPHRENIA AND BIPOLAR DISORDER , 2010, Schizophrenia Research.

[36]  Manuel Desco,et al.  Gyral and Sulcal Cortical Thinning in Adolescents with First Episode Early-Onset Psychosis , 2009, Biological Psychiatry.

[37]  S. Lawrie,et al.  Progressive temporal lobe grey matter loss in adolescents with schizotypal traits and mild intellectual impairment , 2009, Psychiatry Research: Neuroimaging.

[38]  J Ormel,et al.  Schizotypy and brain structure: a voxel-based morphometry study , 2009, Psychological Medicine.

[39]  Reginald S. Lee,et al.  Multilevel Modeling: A Review of Methodological Issues and Applications , 2009 .

[40]  Monte S. Buchsbaum,et al.  Cortical gray and white matter volume in unmedicated schizotypal and schizophrenia patients , 2008, Schizophrenia Research.

[41]  R. Bentall,et al.  Psychological factors in people at ultra-high risk of psychosis: comparisons with non-patients and associations with symptoms , 2006, Psychological Medicine.

[42]  S. Lewis,et al.  The Presence of Neurological Soft Signs Along the Psychosis Proneness Continuum , 2005, Schizophrenia bulletin.

[43]  R. Woods,et al.  Cortical Thinning in Cingulate and Occipital Cortices in First Episode Schizophrenia , 2005, Biological Psychiatry.

[44]  Marianna D. Eddy,et al.  Regionally localized thinning of the cerebral cortex in schizophrenia , 2003, Schizophrenia Research.

[45]  R. McCarley,et al.  The brain in schizotypal personality disorder: a review of structural MRI and CT findings. , 2002, Harvard review of psychiatry.

[46]  Alan C. Evans,et al.  Focal gray matter density changes in schizophrenia. , 2001, Archives of general psychiatry.

[47]  J. Rapoport,et al.  Mapping adolescent brain change reveals dynamic wave of accelerated gray matter loss in very early-onset schizophrenia , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[48]  A W Toga,et al.  Brain abnormalities in early-onset schizophrenia spectrum disorder observed with statistical parametric mapping of structural magnetic resonance images. , 2000, The American journal of psychiatry.

[49]  P. McKenna,et al.  Schizophrenia – a Brain Disease? a Critical Review of Structural and Functional Cerebral Abnormality in the Disorder , 1995, British Journal of Psychiatry.