Bilateral hippocampal increase following first-episode psychosis is associated with good clinical, functional and cognitive outcomes

Background Hippocampal pathology has been proposed to underlie clinical, functional and cognitive impairments in schizophrenia. The hippocampus is a highly plastic brain region; examining change in volume, or change bilaterally, over time, can advance understanding of the substrate of recovery in psychosis. Method Magnetic resonance imaging and outcome data were collected at baseline and 6-year follow-up in 42 first-episode psychosis subjects and 32 matched controls, to investigate whether poorer outcomes are associated with loss of global matter and hippocampal volumes. Bilateral hippocampal increase (BHI) over time, as a marker of hippocampal plasticity was hypothesized to be associated with better outcomes. Regression analyses were performed on: (i) clinical and functional outcomes with grey matter volume change and BHI as predictor variables; and (ii) cognitive outcome with BHI as predictor. Results BHI was present in 29% of psychosis participants. There was no significant grey matter loss over time in either patient or control groups. Less severe illness course and lesser symptom severity were associated with BHI, but not with grey matter change. Employment and global function were associated with BHI and with less grey matter loss. Superior delayed verbal recall was also associated with BHI. Conclusions BHI occurs in a minority of patients following their first psychotic episode and is associated with good outcome across clinical, functional and cognitive domains.

[1]  R. Murray,et al.  The Myth of Schizophrenia as a Progressive Brain Disease , 2012, Schizophrenia bulletin.

[2]  F. Walker,et al.  Stress and inflammation: an emerging story. , 2013 .

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

[4]  Martha Elizabeth Shenton,et al.  Longitudinal loss of gray matter volume in patients with first-episode schizophrenia: DARTEL automated analysis and ROI validation , 2012, NeuroImage.

[5]  J. Ballenger,et al.  Are There Progressive Brain Changes in Schizophrenia? A Meta-Analysis of Structural Magnetic Resonance Imaging Studies , 2012 .

[6]  Nancy C. Andreasen,et al.  Progressive Brain Change in Schizophrenia: A Prospective Longitudinal Study of First-Episode Schizophrenia , 2011, Biological Psychiatry.

[7]  Anthony A Grace,et al.  Hippocampal dysregulation of dopamine system function and the pathophysiology of schizophrenia. , 2011, Trends in pharmacological sciences.

[8]  E. Bullmore,et al.  The University of Birmingham ( Live System ) Are There Progressive Brain Changes in Schizophrenia ? A Meta-Analysis of Structural Magnetic Resonance Imaging Studies , 2016 .

[9]  R. Murray,et al.  Stress and inflammation reduce brain-derived neurotrophic factor expression in first-episode psychosis: a pathway to smaller hippocampal volume. , 2011, The Journal of clinical psychiatry.

[10]  R. Murray,et al.  Lack of progression of brain abnormalities in first-episode psychosis: a longitudinal magnetic resonance imaging study , 2010, Psychological Medicine.

[11]  A. Wagner,et al.  The hippocampal formation in schizophrenia. , 2010, The American journal of psychiatry.

[12]  Robin M. Murray,et al.  Higher cortisol levels are associated with smaller left hippocampal volume in first-episode psychosis , 2010, Schizophrenia Research.

[13]  Peter Falkai,et al.  Hippocampal plasticity in response to exercise in schizophrenia. , 2010, Archives of general psychiatry.

[14]  Christos Pantelis,et al.  Cognitive functioning in schizophrenia, schizoaffective disorder and affective psychoses: meta-analytic study , 2009, British Journal of Psychiatry.

[15]  S. Bouix,et al.  A prospective longitudinal volumetric MRI study of superior temporal gyrus gray matter and amygdala–hippocampal complex in chronic schizophrenia , 2009, Schizophrenia Research.

[16]  Florin Dolcos,et al.  The role of trauma-related distractors on neural systems for working memory and emotion processing in posttraumatic stress disorder. , 2009, Journal of psychiatric research.

[17]  E. Bullmore,et al.  Meta-Analysis of Gray Matter Anomalies in Schizophrenia: Application of Anatomic Likelihood Estimation and Network Analysis , 2008, Biological Psychiatry.

[18]  Hilleke E. Hulshoff Pol,et al.  Progressive Brain Volume Loss in Schizophrenia Over the Course of the Illness: Evidence of Maturational Abnormalities in Early Adulthood , 2008, Biological Psychiatry.

[19]  Alan C. Evans,et al.  Focal Gray Matter Changes in Schizophrenia across the Course of the Illness: A 5-Year Follow-Up Study , 2007, Neuropsychopharmacology.

[20]  J. Lieberman,et al.  Brain volume in first-episode schizophrenia , 2006, British Journal of Psychiatry.

[21]  木下 善弘,et al.  分子精神医学のための臨床評価(第6回)Schedules for Clinical Assessment in Neuropsychiatry(SCAN) , 2006 .

[22]  Robin M. Murray,et al.  Gray matter abnormalities associated with duration of untreated psychosis , 2006, Schizophrenia Research.

[23]  Patricia Desmond,et al.  Hippocampal and amygdala volumes according to psychosis stage and diagnosis: a magnetic resonance imaging study of chronic schizophrenia, first-episode psychosis, and ultra-high-risk individuals. , 2006, Archives of general psychiatry.

[24]  Georg Kemmler,et al.  Longitudinal volumetric MRI study in first- and multiple-episode male schizophrenia patients , 2005, Psychiatry Research: Neuroimaging.

[25]  T. Crow,et al.  Regional deficits in brain volume in schizophrenia: a meta-analysis of voxel-based morphometry studies. , 2005, The American journal of psychiatry.

[26]  John Suckling,et al.  Different Effects of Typical and Atypical Antipsychotics on Grey Matter in First Episode Psychosis: the ÆSOP Study , 2005, Neuropsychopharmacology.

[27]  Guido Gerig,et al.  Duration of illness and treatment effects on hippocampal volume in male patients with schizophrenia , 2005, British Journal of Psychiatry.

[28]  L. DeLisi,et al.  Cerebral ventricular change over the first 10 years after the onset of schizophrenia , 2004, Psychiatry Research: Neuroimaging.

[29]  John Suckling,et al.  The structural brain correlates of neurological soft signs in AESOP first-episode psychoses study. , 2004, Brain : a journal of neurology.

[30]  Ron Kikinis,et al.  Progressive decrease of left Heschl gyrus and planum temporale gray matter volume in first-episode schizophrenia: a longitudinal magnetic resonance imaging study. , 2003, Archives of general psychiatry.

[31]  Stephan Heckers,et al.  Impaired hippocampal recruitment during normal modulation of memory performance in schizophrenia , 2003, Biological Psychiatry.

[32]  R. Kahn,et al.  Brain volume changes in first-episode schizophrenia: a 1-year follow-up study. , 2002, Archives of general psychiatry.

[33]  A. Dale,et al.  Whole Brain Segmentation Automated Labeling of Neuroanatomical Structures in the Human Brain , 2002, Neuron.

[34]  D. Barch,et al.  Working and long-term memory deficits in schizophrenia: is there a common prefrontal mechanism? , 2002, Journal of abnormal psychology.

[35]  Patricia Desmond,et al.  A longitudinal study of hippocampal volume in first episode psychosis and chronic schizophrenia , 2001, Schizophrenia Research.

[36]  E. Laska,et al.  Recovery from psychotic illness: A 15- and 25-year international follow-up study , 2001, British Journal of Psychiatry.

[37]  R. Murray,et al.  Meta-analysis of regional brain volumes in schizophrenia. , 2000, The American journal of psychiatry.

[38]  E T Bullmore,et al.  A modified fuzzy clustering algorithm for operator independent brain tissue classification of dual echo MR images. , 1999, Magnetic resonance imaging.

[39]  Anders M. Dale,et al.  Cortical Surface-Based Analysis I. Segmentation and Surface Reconstruction , 1999, NeuroImage.

[40]  John A. Sweeney,et al.  Superior temporal gyrus and the course of early schizophrenia: progressive, static, or reversible? , 1998, Journal of psychiatric research.

[41]  Tyrone D. Cannon,et al.  A follow-up magnetic resonance imaging study of schizophrenia. Relationship of neuroanatomical changes to clinical and neurobehavioral measures. , 1998, Archives of general psychiatry.

[42]  Alan C. Evans,et al.  A nonparametric method for automatic correction of intensity nonuniformity in MRI data , 1998, IEEE Transactions on Medical Imaging.

[43]  R. Heinrichs,et al.  Neurocognitive deficit in schizophrenia: a quantitative review of the evidence. , 1998, Neuropsychology.

[44]  L. Petrangeli,et al.  Schedules for Clinical Assessment in Neuropsychiatry , 1997, Epidemiologia e Psichiatria Sociale.

[45]  O. Spreen,et al.  A Compendium of Neuropsychological Tests: Administration, Norms, and Commentary , 1991 .

[46]  N C Andreasen,et al.  Negative symptoms in schizophrenia , 1982 .

[47]  Nancy C. Andreasen,et al.  Negative symptoms in schizophrenia , 1982 .

[48]  J. Fleiss,et al.  The global assessment scale. A procedure for measuring overall severity of psychiatric disturbance. , 1976, Archives of general psychiatry.

[49]  M. Annett A classification of hand preference by association analysis. , 1970, British journal of psychology.

[50]  H. M. Luykx,et al.  Duration of illness. , 1961, Human biology.