Medial temporal lobe structure and cognition in individuals with schizophrenia and in their non-psychotic siblings

Medial temporal lobe (MTL) structures play a central role in episodic memory. Prior studies suggest that individuals with schizophrenia have deficits in episodic memory as well as structural abnormalities of the medial temporal lobe (MTL). While correlations have been reported between MTL volume loss and episodic memory deficits in such individuals, it is not clear whether such correlations reflect the influence of the disease state or of underlying genetic influences that might contribute to risk. We used high resolution magnetic resonance imaging and probabilistic algorithms for image analysis to determine whether MTL structure, episodic memory performance and the relationship between the two differed among groups of 47 healthy control subjects, 50 control siblings, 39 schizophrenia subjects, and 33 siblings of schizophrenia subjects. High-dimensional large deformation brain mapping was used to obtain volume measures of the hippocampus. Cortical distance mapping was used to obtain volume and thickness measures of the parahippocampal gyrus (PHG) and its substructures: the entorhinal cortex (ERC), the perirhinal cortex (PRC), and the parahippocampal cortex (PHC). Neuropsychological data was used to establish an episodic memory domain score for each subject. Both schizophrenia subjects and their siblings displayed abnormalities in episodic memory performance. Siblings of individuals with schizophrenia, and to a lesser extent, individuals with schizophrenia themselves, displayed abnormalities in measures of MTL structure (volume loss or cortical thinning) as compared to control groups. Further, we observed correlations between structural measures and memory performance in both schizophrenia subjects and their siblings, but not in their respective control groups. These findings suggest that disease-specific genetic factors present in both patients and their relatives may be responsible for correlated abnormalities of MTL structure and memory impairment. The observed attenuated effect of such factors on MTL structure in individuals with schizophrenia may be due to non-genetic influences related to the development and progression of the disease on global brain structure and cognitive processing.

[1]  Michael I. Miller,et al.  Validation of semiautomated methods for quantifying cingulate cortical metrics in schizophrenia , 2004, Psychiatry Research: Neuroimaging.

[2]  M. Kenward,et al.  Small sample inference for fixed effects from restricted maximum likelihood. , 1997, Biometrics.

[3]  R S Kahn,et al.  Structural brain abnormalities in patients with schizophrenia and their healthy siblings. , 2000, The American journal of psychiatry.

[4]  G. Scotti,et al.  Memory functions and temporal-limbic morphology in schizophrenia , 1993, Psychiatry Research: Neuroimaging.

[5]  Jarmo Hietala,et al.  A volumetric MRI study of the entorhinal cortex in first episode neuroleptic-naive schizophrenia , 2002, Biological Psychiatry.

[6]  H. Nyman Neuropsychological function in schizophrenia , 2002, European Psychiatry.

[7]  M. Egan,et al.  Cognitive impairments in patients with schizophrenia displaying preserved and compromised intellect. , 2000, Archives of general psychiatry.

[8]  René S. Kahn,et al.  Cognitive deficits in relatives of patients with schizophrenia: a meta-analysis , 2004, Schizophrenia Research.

[9]  Nicolette Marshall,et al.  A controlled study of brain structure in monozygotic twins concordant and discordant for schizophrenia , 2004, Biological Psychiatry.

[10]  Renaud Jardri,et al.  Cortical activations during auditory verbal hallucinations in schizophrenia: a coordinate-based meta-analysis. , 2011, The American journal of psychiatry.

[11]  Kristen M. Haut,et al.  The Influence of Encoding Strategy on Episodic Memory and Cortical Activity in Schizophrenia , 2005, Biological Psychiatry.

[12]  Sabrina M. Tom,et al.  Dissociable correlates of recollection and familiarity within the medial temporal lobes , 2004, Neuropsychologia.

[13]  D. Barch,et al.  Elevated rates of substance use disorders in non-psychotic siblings of individuals with schizophrenia , 2008, Schizophrenia Research.

[14]  Bruce Fischl,et al.  An MRI-based method for measuring volume, thickness and surface area of entorhinal, perirhinal, and posterior parahippocampal cortex , 2009, Neurobiology of Aging.

[15]  M. Witter,et al.  A Specific Role of the Human Hippocampus in Recall of Temporal Sequences , 2009, The Journal of Neuroscience.

[16]  Michael I. Miller,et al.  Structural abnormalities in gyri of the prefrontal cortex in individuals with schizophrenia and their unaffected siblings , 2010, British Journal of Psychiatry.

[17]  L. Davachi,et al.  Behavioral/systems/cognitive Functional–neuroanatomic Correlates of Recollection: Implications for Models of Recognition Memory , 2022 .

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

[19]  I. Gottesman,et al.  The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.

[20]  H. Rusinek,et al.  Cognitive performance in schizophrenia: relationship to regional brain volumes and psychiatric symptoms , 2002, Psychiatry Research: Neuroimaging.

[21]  A. Meyer-Lindenberg,et al.  Heritability of Brain Morphology Related to Schizophrenia: A Large-Scale Automated Magnetic Resonance Imaging Segmentation Study , 2008, Biological Psychiatry.

[22]  Luis Martí-Bonmatí,et al.  Increased amygdala and parahippocampal gyrus activation in schizophrenic patients with auditory hallucinations: An fMRI study using independent component analysis , 2010, Schizophrenia Research.

[23]  Guy B. Williams,et al.  The human perirhinal cortex and semantic memory , 2004, The European journal of neuroscience.

[24]  Jerry L. Prince,et al.  Topology correction in brain cortex segmentation using a multiscale, graph-based algorithm , 2002, IEEE Transactions on Medical Imaging.

[25]  Tsutomu Hashikawa,et al.  Cytoarchitectonic and chemoarchitectonic subdivisions of the perirhinal and parahippocampal cortices in macaque monkeys , 2007, The Journal of comparative neurology.

[26]  D. Amend,et al.  Reduced hippocampal N-acetylaspartate without volume loss in schizophrenia , 1999, Schizophrenia Research.

[27]  Carey E. Priebe,et al.  Validation of Alternating Kernel Mixture Method: Application to Tissue Segmentation of Cortical and Subcortical Structures , 2008, Journal of biomedicine & biotechnology.

[28]  M. Bar,et al.  The parahippocampal cortex mediates spatial and nonspatial associations. , 2007, Cerebral cortex.

[29]  J. Pruessner,et al.  Selective abnormal modulation of hippocampal activity during memory formation in first-episode psychosis. , 2007, Archives of general psychiatry.

[30]  Lei Wang,et al.  Hippocampal deformities in the unaffected siblings of schizophrenia subjects , 2003, Biological Psychiatry.

[31]  R. Kahn,et al.  Memory impairment in schizophrenia: a meta-analysis. , 1999, The American journal of psychiatry.

[32]  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.

[33]  M. Miller,et al.  Hippocampal deformities in schizophrenia characterized by high dimensional brain mapping. , 2002, The American journal of psychiatry.

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

[35]  R. Freedman,et al.  Studies on the hippocampal formation: From basic development to clinical applications: Studies on schizophrenia , 2010, Progress in Neurobiology.

[36]  Rutger Goekoop,et al.  Deactivation of the parahippocampal gyrus preceding auditory hallucinations in schizophrenia. , 2010, The American journal of psychiatry.

[37]  Michael I. Miller,et al.  Basal Ganglia Shape Abnormalities in the Unaffected Siblings of Schizophrenia Patients , 2008, Biological Psychiatry.

[38]  J. Fleiss,et al.  Intraclass correlations: uses in assessing rater reliability. , 1979, Psychological bulletin.

[39]  Raymond C K Chan,et al.  Facial emotion processing in schizophrenia: a meta-analysis of functional neuroimaging data. , 2010, Schizophrenia bulletin.

[40]  J. Lieberman,et al.  Antipsychotic drug effects on brain morphology in first-episode psychosis. , 2005, Archives of general psychiatry.

[41]  R. Kahn,et al.  Volumes of brain structures in twins discordant for schizophrenia. , 2001, Archives of general psychiatry.

[42]  B. Turetsky,et al.  Event-related fMRI of frontotemporal activity during word encoding and recognition in schizophrenia. , 2004, The American journal of psychiatry.

[43]  R. Insausti,et al.  The parahippocampal gyrus in the baboon: anatomical, cytoarchitectonic and magnetic resonance imaging (MRI) studies. , 2004, Cerebral cortex.

[44]  Alexander Hammers,et al.  Evidence of a smaller left hippocampus and left temporal horn in both patients with first episode schizophrenia and normal control subjects , 2000, Psychiatry Research: Neuroimaging.

[45]  Konstantine K. Zakzanis,et al.  Neurocognitive Deficit in Schizophrenia: A Quantitative Review of the Evidence , 1998 .

[46]  Stephan Heckers,et al.  Hippocampal and parahippocampal volumes in schizophrenia: a structural MRI study. , 2006, Schizophrenia bulletin.

[47]  Sabina M. Gonzales,et al.  Prefrontal activation deficits during episodic memory in schizophrenia. , 2009, The American journal of psychiatry.

[48]  Andrea Federspiel,et al.  New evidence for involvement of the entorhinal region in schizophrenia: a combined MRI volumetric and DTI study , 2005, NeuroImage.

[49]  M. Keshavan,et al.  Parahippocampal gyrus in first episode psychotic disorders: a structural magnetic resonance imaging study , 2004, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[50]  James D. Christensen,et al.  Cerebral Cortical Gray Expansion Associated with Two Second-Generation Antipsychotics , 2005, Biological Psychiatry.

[51]  Andy C. H. Lee,et al.  Differentiating the Roles of the Hippocampus and Perirhinal Cortex in Processes beyond Long-Term Declarative Memory: A Double Dissociation in Dementia , 2006, The Journal of Neuroscience.

[52]  L. DeLisi,et al.  Schizophrenia as a chronic active brain process: a study of progressive brain structural change subsequent to the onset of schizophrenia , 1997, Psychiatry Research: Neuroimaging.

[53]  Alan C. Evans,et al.  Amygdala–hippocampal volume and verbal memory in first-degree relatives of schizophrenic patients , 2001, Psychiatry Research: Neuroimaging.

[54]  H. Soininen,et al.  MR volumetric analysis of the human entorhinal, perirhinal, and temporopolar cortices. , 1998, AJNR. American journal of neuroradiology.

[55]  Denis Dooley,et al.  Atlas of the Human Brain. , 1971 .

[56]  Lei Wang,et al.  Thalamic Shape Abnormalities in Individuals with Schizophrenia and Their Nonpsychotic Siblings , 2007, The Journal of Neuroscience.

[57]  Carey E. Priebe,et al.  Segmenting magnetic resonance images via hierarchical mixture modelling , 2006, Comput. Stat. Data Anal..

[58]  Robert A. Bornstein,et al.  The Wechsler Memory Scale—Revised , 1990 .

[59]  David R Roalf,et al.  Decrements in volume of anterior ventromedial temporal lobe and olfactory dysfunction in schizophrenia. , 2003, Archives of general psychiatry.

[60]  E. Kaplan,et al.  Integrating clinical assessment with cognitive neuroscience: construct validation of the California Verbal Learning Test. , 1988, Journal of consulting and clinical psychology.

[61]  Michael I. Miller,et al.  Cingulate gyrus neuroanatomy in schizophrenia subjects and their non-psychotic siblings , 2008, Schizophrenia Research.

[62]  M. Miller,et al.  Statistical Analysis of Hippocampal Asymmetry in Schizophrenia , 2001, NeuroImage.

[63]  Nikos Makris,et al.  Left hippocampal volume as a vulnerability indicator for schizophrenia: a magnetic resonance imaging morphometric study of nonpsychotic first-degree relatives. , 2002, Archives of general psychiatry.

[64]  Vincent Magnotta,et al.  Hippocampal volume deficits and shape deformities in young biological relatives of schizophrenia probands , 2010, NeuroImage.

[65]  R. Gur,et al.  Neuropsychological function in schizophrenia. Selective impairment in memory and learning. , 1991, Archives of general psychiatry.

[66]  Kelly Rehm,et al.  Regionally specific cortical thinning and gray matter abnormalities in the healthy relatives of schizophrenia patients. , 2006, Cerebral cortex.

[67]  K. Hawkins,et al.  Memory deficits in patients with schizophrenia: preliminary data from the Wechsler Memory Scale-Third Edition support earlier findings. , 1999, Journal of psychiatry & neuroscience : JPN.

[68]  U. Grenander,et al.  Hippocampal morphometry in schizophrenia by high dimensional brain mapping. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[69]  Jason P. Mitchell,et al.  Multiple routes to memory: Distinct medial temporal lobe processes build item and source memories , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[70]  C. Reynolds,et al.  Wechsler memory scale-revised , 1988 .

[71]  A. Gharabaghi,et al.  The parahippocampal gyrus as a multimodal association area in psychosis , 2010, Journal of Clinical Neuroscience.

[72]  Deanna M Barch,et al.  Factors mediating cognitive deficits and psychopathology among siblings of individuals with schizophrenia. , 2005, Schizophrenia bulletin.

[73]  Eve C. Johnstone,et al.  Structural Gray Matter Differences between First-Episode Schizophrenics and Normal Controls Using Voxel-Based Morphometry , 2002, NeuroImage.

[74]  J. Jolles,et al.  Cognitive performance in relation to MRI temporal lobe volume in schizophrenic patients and healthy control subjects. , 2000, The Journal of neuropsychiatry and clinical neurosciences.