Magnetic source imaging evidence of sex differences in cerebral lateralization in schizophrenia.

BACKGROUND It has been postulated that schizophrenia represents a disorder of anomalous cerebral lateralization. This study is a replication of earlier preliminary findings using a multichannel neuromagnetometer, suggesting altered lateralization in schizophrenia in male subjects, with an extension of the findings to female subjects. METHODS We used magnetoencephalography-based magnetic source imaging to estimate the intracranial location of the 100-millisecond latency auditory-evoked field component (M100) in both left and right hemispheres of 20 patients with paranoid schizophrenia and 20 controls without schizophrenia. Neuroanatomical data were obtained by means of magnetic resonance imaging, from which we segmented and computed volumes of both total brain and left and right superior temporal gyri. RESULTS Locations of M100 source were compatible with neuronal generators located in the transverse gyri of Heschl on the superior temporal gyri in both study groups; M100 sources were asymmetric in all the control subjects. The male patient subgroup exhibited significantly less asymmetry than the control group, while the female patient subgroup actually showed significantly more asymmetry. The male patient subgroup generally had smaller superior temporal gyri than the control group. No evidence of total brain volume differences was observed. CONCLUSIONS Our findings support previous magnetoencephalography-based studies suggesting anomalous cerebral lateralization in schizophrenia. Further, in extending our studies to female patients, our data suggest that the nature of this anomaly is sex specific, a finding that, to our knowledge, has not previously been reported.

[1]  P. Teale,et al.  Reproducibility of MEG auditory evoked field source localizations in normal human subjects using a seven-channel gradiometer , 1996, IEEE Transactions on Biomedical Engineering.

[2]  P. Teale,et al.  MEG based brain laterality: Sex differences in normal adults , 1995, Neuropsychologia.

[3]  B. Rockstroh,et al.  Increased Cortical Representation of the Fingers of the Left Hand in String Players , 1995, Science.

[4]  L. DeLisi,et al.  A prospective follow-up study of brain morphology and cognition in first-episode schizophrenic patients: Preliminary findings , 1995, Biological Psychiatry.

[5]  A. Alavi,et al.  Resting cerebral glucose metabolism in first-episode and previously treated patients with schizophrenia relates to clinical features. , 1995, Archives of general psychiatry.

[6]  J. Lieberman,et al.  Gender differences in onset of illness, treatment response, course, and biologic indexes in first-episode schizophrenic patients. , 1995, The American journal of psychiatry.

[7]  G D Pearlson,et al.  Reversal of asymmetry of the planum temporale in schizophrenia. , 1995, The American journal of psychiatry.

[8]  R. Oades,et al.  Serum gonadal steroid hormones in young schizophrenic patients , 1994, Psychoneuroendocrinology.

[9]  G. Fein,et al.  31Phosphorus magnetic resonance spectroscopy of the frontal and parietal lobes in chronic schizophrenia , 1994, Biological Psychiatry.

[10]  J. Ehrhardt,et al.  Thalamic abnormalities in schizophrenia visualized through magnetic resonance image averaging. , 1994, Science.

[11]  M Ashtari,et al.  Absence of regional hemispheric volume asymmetries in first-episode schizophrenia. , 1994, The American journal of psychiatry.

[12]  A. Riecher-Rössler,et al.  Further evidence for a specific role of estradiol in schizophrenia? , 1994, Biological Psychiatry.

[13]  A. Riecher-Rössler,et al.  Influence of the menstrual cycle phase on the therapeutic response in schizophrenia , 1994, Biological Psychiatry.

[14]  P. Teale,et al.  Auditory M100 component 1: relationship to Heschl's gyri. , 1994, Brain research. Cognitive brain research.

[15]  G. Pearlson,et al.  Decreased regional cortical gray matter volume in schizophrenia. , 1994, The American journal of psychiatry.

[16]  Edith V. Sullivan,et al.  Volumetric MRI assessment of temporal lobe structures in schizophrenia , 1994, Biological Psychiatry.

[17]  Tyrone D. Cannon,et al.  Clinical subtypes of schizophrenia: differences in brain and CSF volume. , 1994, The American journal of psychiatry.

[18]  Douglas W. Jones,et al.  Gender differences in the normal lateralization of the supratemporal cortex: MRI surface-rendering morphometry of Heschl's gyrus and the planum temporale. , 1994, Cerebral cortex.

[19]  F E Bloom,et al.  Intrasubject reliability and validity of somatosensory source localization using a large array biomagnetometer. , 1994, Electroencephalography and clinical neurophysiology.

[20]  T. Paolo Modulation of brain dopamine transmission by sex steroids. , 1994 .

[21]  S M Breedlove,et al.  Sexual differentiation of the human nervous system. , 1994, Annual review of psychology.

[22]  A. Riecher-Rössler,et al.  Can estradiol modulate schizophrenic symptomatology? , 1994, Schizophrenia bulletin.

[23]  Douglas W. Jones,et al.  Sylvian fissure asymmetries in monozygotic twins: A test of laterality in schizophrenia , 1993, Biological Psychiatry.

[24]  A. Riecher-Rössler,et al.  Generating and testing a causal explanation of the gender difference in age at first onset of schizophrenia , 1993, Psychological Medicine.

[25]  R. Hemmingsen,et al.  Computerised Tomography in Newly Diagnosed Schizophrenia and Schizophreniform Disorder , 1993, British Journal of Psychiatry.

[26]  J. Waddington Schizophrenia: developmental neuroscience and pathobiology , 1993, The Lancet.

[27]  John W. Haller,et al.  Lateralized attentional abnormality in schizophrenia is correlated with severity of symptoms , 1993, Biological Psychiatry.

[28]  A. Riecher-Rössler,et al.  The Influence of Age and Sex on the Onset and Early Course of Schizophrenia , 1993, British Journal of Psychiatry.

[29]  J. Waddington,et al.  Neurodynamics of abnormalities in cerebral metabolism and structure in schizophrenia. , 1993, Schizophrenia bulletin.

[30]  L. Kaufman,et al.  Behavioral lifetime of human auditory sensory memory predicted by physiological measures. , 1992, Science.

[31]  R. Buchanan,et al.  Brain morphology and schizophrenia. A magnetic resonance imaging study of limbic, prefrontal cortex, and caudate structures. , 1992, Archives of general psychiatry.

[32]  M. LeMay,et al.  Abnormalities of the left temporal lobe and thought disorder in schizophrenia. A quantitative magnetic resonance imaging study. , 1992, The New England journal of medicine.

[33]  E. Bigler,et al.  Hemisphere size asymmetry predicts relative verbal and nonverbal intelligence differently in the sexes: An MRI study of structure—Function relations , 1992 .

[34]  Peter Falkai,et al.  Loss of sylvian fissure asymmetry in schizophrenia A quantitative post mortem study , 1992, Schizophrenia Research.

[35]  L. Kaufman,et al.  Human auditory primary and association cortex have differing lifetimes for activation traces , 1992, Brain Research.

[36]  M Kajola,et al.  Modified activity of the human auditory cortex during auditory hallucinations. , 1992, The American journal of psychiatry.

[37]  James C. Ehrhardt,et al.  Subcortical and temporal structures in affective disorder and schizophrenia: A magnetic resonance imaging study , 1992, Biological Psychiatry.

[38]  L. DeLisi,et al.  Anomalous lateral sulcus asymmetry and cognitive function in first-episode schizophrenia. , 1992, Schizophrenia bulletin.

[39]  P. Teale,et al.  Magnetic auditory M100 source location in normal females , 1991, Brain Research Bulletin.

[40]  A. Scheibel,et al.  Hippocampal pyramidal cell disarray in schizophrenia as a bilateral phenomenon. , 1991, Archives of general psychiatry.

[41]  N. Andreasen,et al.  The role of gender in studies of ventricle enlargement in schizophrenia: a predominantly male effect. , 1990, The American journal of psychiatry.

[42]  S. Sholl,et al.  Androgen receptors are differentially distributed between right and left cerebral hemispheres of the fetal male rhesus monkey , 1990, Brain Research.

[43]  J. Ehrhardt,et al.  Magnetic resonance imaging of the brain in schizophrenia. The pathophysiologic significance of structural abnormalities. , 1990, Archives of general psychiatry.

[44]  P. Flor-Henry Influence of gender in schizophrenia as related to other psychopathological syndromes. , 1990, Schizophrenia bulletin.

[45]  J. Goldstein,et al.  Gender and the course of schizophrenia: differences in treated outcomes. , 1990, Schizophrenia bulletin.

[46]  T. Crow Temporal lobe asymmetries as the key to the etiology of schizophrenia. , 1990, Schizophrenia bulletin.

[47]  M. Tsuang,et al.  The role of gender in identifying subtypes of schizophrenia: a latent class analytic approach. , 1990, Schizophrenia bulletin.

[48]  H. Nasrallah,et al.  Gender differences in schizophrenia on MRI brain scans. , 1990, Schizophrenia bulletin.

[49]  M. Seeman,et al.  The role of estrogens in schizophrenia gender differences. , 1990, Schizophrenia bulletin.

[50]  P. Teale,et al.  Late auditory magnetic sources may differ in the left hemisphere of schizophrenic patients. A preliminary report. , 1989, Archives of general psychiatry.

[51]  M Reite,et al.  Source location of a 50 msec latency auditory evoked field component. , 1988, Electroencephalography and clinical neurophysiology.

[52]  P. Teale,et al.  Source origin of a 50-msec latency auditory evoked field component in young schizophrenic men , 1988, Biological Psychiatry.

[53]  J. Goldstein Gender differences in the course of schizophrenia. , 1988, The American journal of psychiatry.

[54]  K. Lehnertz,et al.  Tonotopic organization of the human auditory cortex revealed by transient auditory evoked magnetic fields. , 1988, Electroencephalography and clinical neurophysiology.

[55]  Bruce G. Link,et al.  Gender and the expression of schizophrenia. , 1988, Journal of Psychiatric Research.

[56]  J. Sarvas Basic mathematical and electromagnetic concepts of the biomagnetic inverse problem. , 1987, Physics in medicine and biology.

[57]  B. Bogerts,et al.  Basal Ganglia and Limbic System Pathology in Schizophrenia: A Morphometric Study of Brain Volume and Shrinkage , 1985 .

[58]  N. Geschwind,et al.  Cerebral lateralization. Biological mechanisms, associations, and pathology: I. A hypothesis and a program for research. , 1985, Archives of neurology.

[59]  A. Loranger Sex difference in age at onset of schizophrenia. , 1984, Archives of general psychiatry.

[60]  S. Bressler,et al.  Shadows of thought: shifting lateralization of human brain electrical patterns during brief visuomotor task. , 1983, Science.

[61]  L. Kaufman,et al.  Tonotopic organization of the human auditory cortex. , 1982, Science.

[62]  D. Weinberger,et al.  Asymmetrical volumes of the right and left frontal and occipital regions of the human brain , 1982, Annals of neurology.

[63]  A. Oke,et al.  Lateralization of norepinephrine in human thalamus. , 1978, Science.

[64]  E. Robins,et al.  Research diagnostic criteria: rationale and reliability. , 1978, Archives of general psychiatry.

[65]  N. Geschwind,et al.  Right-left asymmetrics in the brain. , 1978, Science.

[66]  John M. Davis Dose equivalence of the anti-psychotic drugs , 1974 .

[67]  M. Merzenich,et al.  Representation of the cochlear partition of the superior temporal plane of the macaque monkey. , 1973, Brain research.

[68]  A. Forrest,et al.  SEX DIFFERENCES AND THE SCHIZOPHRENIC EXPERIENCE , 1971, Acta psychiatrica Scandinavica.

[69]  A. Tunturi A difference in the representation of auditory signals for the left and right ears in the iso-frequency contours of the right middle ectosylvian auditory cortex of the dog. , 1952, The American journal of physiology.