Impaired temporoparietal deactivation with working memory load in antipsychotic-naïve patients with first-episode schizophrenia

Abstract Objectives. Neuroimaging studies have shown abnormal task-related deactivations during working memory (WM) in schizophrenia patients with recent emphasis on brain regions within the default mode network. Using fMRI, we tested whether antipsychotic-naïve schizophrenia patients were impaired at deactivating brain regions that do not subserve WM. Methods. Twenty-three antipsychotic-naïve patients with first-episode schizophrenia and 35 healthy individuals underwent whole-brain 3T fMRI scans while performing a verbal N-back task including 0-back (no WM load), 1-back (low WM load), and 2-back (high WM load) conditions. Results. Contrasting the 2-back and 0-back conditions revealed that patients deactivated default mode network regions to a similar degree as controls. However, patients were impaired in deactivating large bilateral clusters centred on the superior temporal gyrus with increasing WM load. These regions activated with the no WM load condition (0-back) in both groups. Conclusions. Because 0-back activation reflects verbal attention processes, patients’ persistent activation in the 1-back and 2-back conditions may reflect an inability to shift cognitive strategy with onset of WM demands. Since patients were antipsychotic-naïve and task performance was equal to controls, we infer that this impaired temporoparietal deactivation may represent a primary dysfunction in schizophrenia.

[1]  Karl J. Friston,et al.  Multisubject fMRI Studies and Conjunction Analyses , 1999, NeuroImage.

[2]  V. Calhoun,et al.  Aberrant "default mode" functional connectivity in schizophrenia. , 2007, The American journal of psychiatry.

[3]  E. Bramon,et al.  Spatial working memory in individuals at high risk for psychosis: Longitudinal fMRI study , 2010, Schizophrenia Research.

[4]  Karl J. Friston,et al.  Modelling Geometric Deformations in Epi Time Series , 2022 .

[5]  H. Walter,et al.  Changes over time in frontotemporal activation during a working memory task in patients with schizophrenia , 2007, Schizophrenia Research.

[6]  Peter Falkai,et al.  Disturbed functional connectivity within brain networks subserving domain-specific subcomponents of working memory in schizophrenia: relation to performance and clinical symptoms. , 2010, Journal of psychiatric research.

[7]  M. D’Esposito,et al.  Functional MRI studies of spatial and nonspatial working memory. , 1998, Brain research. Cognitive brain research.

[8]  Karl J. Friston,et al.  Movement‐Related effects in fMRI time‐series , 1996, Magnetic resonance in medicine.

[9]  T. Brugha,et al.  SCAN. Schedules for Clinical Assessment in Neuropsychiatry. , 1990, Archives of general psychiatry.

[10]  R. C. Oldfield The assessment and analysis of handedness: the Edinburgh inventory. , 1971, Neuropsychologia.

[11]  Edward E. Smith,et al.  Temporal dynamics of brain activation during a working memory task , 1997, Nature.

[12]  O. Paulson,et al.  Hippocampal and caudate volume reductions in antipsychotic-naive first-episode schizophrenia. , 2010, Journal of psychiatry & neuroscience : JPN.

[13]  D. Barch,et al.  Imaging genetic liability to schizophrenia: systematic review of FMRI studies of patients' nonpsychotic relatives. , 2009, Schizophrenia bulletin.

[14]  P. Mcguire,et al.  Neuroimaging predictors of transition to psychosis—A systematic review and meta-analysis , 2010, Neuroscience & Biobehavioral Reviews.

[15]  D. Manoach Prefrontal cortex dysfunction during working memory performance in schizophrenia: reconciling discrepant findings , 2003, Schizophrenia Research.

[16]  F. Castellanos,et al.  Spontaneous attentional fluctuations in impaired states and pathological conditions: A neurobiological hypothesis , 2007, Neuroscience & Biobehavioral Reviews.

[17]  Neil A. Macmillan,et al.  Detection Theory: A User's Guide , 1991 .

[18]  H. Walter,et al.  Temporally anticorrelated brain networks during working memory performance reveal aberrant prefrontal and hippocampal connectivity in patients with schizophrenia , 2009, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[19]  Karl J. Friston,et al.  Reduced frontotemporal functional connectivity in schizophrenia associated with auditory hallucinations , 2002, Biological Psychiatry.

[20]  M. Egan,et al.  Complexity of prefrontal cortical dysfunction in schizophrenia: more than up or down. , 2003, The American journal of psychiatry.

[21]  Junghee Lee,et al.  Working memory impairments in schizophrenia: a meta-analysis. , 2005, Journal of abnormal psychology.

[22]  M. Greicius,et al.  Default-Mode Activity during a Passive Sensory Task: Uncoupled from Deactivation but Impacting Activation , 2004, Journal of Cognitive Neuroscience.

[23]  C. Svarer,et al.  Decreased frontal serotonin2A receptor binding in antipsychotic-naive patients with first-episode schizophrenia. , 2010, Archives of general psychiatry.

[24]  Jennifer L. Mozolic,et al.  Cross-modal deactivations during modality-specific selective attention , 2008, BMC neurology.

[25]  R. Murray,et al.  Neural correlates of formal thought disorder in schizophrenia: preliminary findings from a functional magnetic resonance imaging study. , 2001, Archives of general psychiatry.

[26]  D. Glahn,et al.  Beyond hypofrontality: A quantitative meta‐analysis of functional neuroimaging studies of working memory in schizophrenia , 2005, Human brain mapping.

[27]  Russell A. Poldrack,et al.  The effect of working memory performance on functional MRI in schizophrenia , 2005, Schizophrenia Research.

[28]  R. Murray,et al.  Mapping auditory hallucinations in schizophrenia using functional magnetic resonance imaging. , 2000, Archives of general psychiatry.

[29]  Karl J. Friston,et al.  Brain activations in schizophrenia during a graded memory task studied with functional neuroimaging. , 1998, Archives of general psychiatry.

[30]  Karl J. Friston,et al.  Regional Brain Activity in Chronic Schizophrenic Patients during the Performance of a Verbal Fluency Task , 1995, British Journal of Psychiatry.

[31]  Murat Yücel,et al.  Task-induced deactivation of midline cortical regions in schizophrenia assessed with fMRI , 2007, Schizophrenia Research.

[32]  Greg G. Brown,et al.  Dysregulation of working memory and default‐mode networks in schizophrenia using independent component analysis, an fBIRN and MCIC study , 2009, Human brain mapping.

[33]  J. Gabrieli,et al.  Hyperactivity and hyperconnectivity of the default network in schizophrenia and in first-degree relatives of persons with schizophrenia , 2009, Proceedings of the National Academy of Sciences.

[34]  Henrik Walter,et al.  Working memory dysfunction in schizophrenia compared to healthy controls and patients with depression: Evidence from event-related fMRI , 2007, NeuroImage.

[35]  C. D. Frith,et al.  Abnormal monitoring of inner speech: a physiological basis for auditory hallucinations , 1995, The Lancet.

[36]  J. Binder,et al.  A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging , 2003, Journal of Cognitive Neuroscience.

[37]  G L Shulman,et al.  INAUGURAL ARTICLE by a Recently Elected Academy Member:A default mode of brain function , 2001 .

[38]  C. Chabris,et al.  Neural mechanisms of general fluid intelligence , 2003, Nature Neuroscience.

[39]  A. Meyer-Lindenberg,et al.  Dysfunctional prefrontal regional specialization and compensation in schizophrenia. , 2006, The American journal of psychiatry.

[40]  A. Baddeley,et al.  The multi-component model of working memory: Explorations in experimental cognitive psychology , 2006, Neuroscience.

[41]  Elvira Bramon,et al.  Superior temporal lobe dysfunction and frontotemporal dysconnectivity in subjects at risk of psychosis and in first-episode psychosis , 2011 .

[42]  Anders M. Dale,et al.  Reliability in multi-site structural MRI studies: Effects of gradient non-linearity correction on phantom and human data , 2006, NeuroImage.

[43]  Karl J. Friston,et al.  Local and Distributed Effects of Apomorphine on Fronto-Temporal Function in Acute Unmedicated Schizophrenia , 1996, The Journal of Neuroscience.

[44]  Paul Allen,et al.  Neural correlates of the misattribution of speech in schizophrenia , 2007, British Journal of Psychiatry.

[45]  V Menon,et al.  Modality effects in verbal working memory: differential prefrontal and parietal responses to auditory and visual stimuli , 2004, NeuroImage.

[46]  Karl J. Friston,et al.  Schizophrenia: a disconnection syndrome? , 1995, Clinical neuroscience.

[47]  M. Chee,et al.  fMRI study of maintenance and manipulation processes within working memory in first-episode schizophrenia. , 2005, The American journal of psychiatry.

[48]  Fabio Sambataro,et al.  Treatment with Olanzapine is Associated with Modulation of the Default Mode Network in Patients with Schizophrenia , 2010, Neuropsychopharmacology.

[49]  J B Poline,et al.  Evidence for abnormal cortical functional connectivity during working memory in schizophrenia. , 2001, The American journal of psychiatry.

[50]  E. Bramon,et al.  Superior temporal lobe dysfunction and frontotemporal dysconnectivity in subjects at risk of psychosis and in first‐episode psychosis , 2009, Human brain mapping.

[51]  Philip K. McGuire,et al.  Neural correlates of executive function and working memory in the ‘at-risk mental state’ , 2007, British Journal of Psychiatry.

[52]  R. Salvador,et al.  Failure to deactivate in the prefrontal cortex in schizophrenia: dysfunction of the default mode network? , 2008, Psychological Medicine.

[53]  G. Shulman,et al.  Medial prefrontal cortex and self-referential mental activity: Relation to a default mode of brain function , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[54]  E. Bullmore,et al.  Effects of gamma-aminobutyric acid-modulating drugs on working memory and brain function in patients with schizophrenia. , 2007, Archives of general psychiatry.

[55]  C. Frith,et al.  Functional neuroanatomy of verbal self-monitoring , 1996, NeuroImage.

[56]  Maurizio Corbetta,et al.  The human brain is intrinsically organized into dynamic, anticorrelated functional networks. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[57]  S. Kay,et al.  The positive and negative syndrome scale (PANSS) for schizophrenia. , 1987, Schizophrenia bulletin.

[58]  R H Logie,et al.  Visuospatial working memory, movement control and executive demands. , 1995, British journal of psychology.

[59]  C. Frith,et al.  Pathophysiology of ‘positive’ thought disorder in schizophrenia , 1998, British Journal of Psychiatry.