Advertisement
Original article| Volume 48, ISSUE 2, P147-162, July 15, 2000

An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia

  • Lori L Altshuler
    Correspondence
    Address reprint requests to Lori L. Altshuler, M.D., UCLA Mood Disorders Research Program, 300 UCLA Medical Plaza, Suite 1544, Los Angeles CA 90095
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)

    Psychiatry Service, West Los Angeles VA Medical Center, Los Angeles, California, USA (LLA, GB, JW, RG, JM)
    Search for articles by this author
  • George Bartzokis
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)

    Psychiatry Service, West Los Angeles VA Medical Center, Los Angeles, California, USA (LLA, GB, JW, RG, JM)

    Department of Psychiatry, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA (GB)

    Psychiatry Service, Little Rock VA Medical Center, North Little Rock, Arkansas, USA (GB), Arkansas
    Search for articles by this author
  • Tom Grieder
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)
    Search for articles by this author
  • John Curran
    Affiliations
    Department of Radiological Sciences, UCLA Medical Center, Los Angeles, California, USA (JC), Los Angeles, California
    Search for articles by this author
  • Tanya Jimenez
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)
    Search for articles by this author
  • Kristin Leight
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)
    Search for articles by this author
  • Jeffery Wilkins
    Affiliations
    Psychiatry Service, West Los Angeles VA Medical Center, Los Angeles, California, USA (LLA, GB, JW, RG, JM)
    Search for articles by this author
  • Robert Gerner
    Affiliations
    Psychiatry Service, West Los Angeles VA Medical Center, Los Angeles, California, USA (LLA, GB, JW, RG, JM)
    Search for articles by this author
  • Jim Mintz
    Affiliations
    Department of Psychiatry, UCLA Neuropsychiatric Institute, Los Angeles, California, USA (LLA, GB, TG, TJ, KL, JM)

    Psychiatry Service, West Los Angeles VA Medical Center, Los Angeles, California, USA (LLA, GB, JW, RG, JM)
    Search for articles by this author

      Abstract

      Background: Hippocampal atrophy has been described in postmortem and magnetic resonance imaging studies of schizophrenia. The specificity of this finding to schizophrenia remains to be determined. The neuropathology of bipolar disorder is understudied, and temporal lobe structures have only recently been evaluated.
      Methods: Twenty-four bipolar, 20 schizophrenic, and 18 normal comparison subjects were evaluated using magnetic resonance brain imaging. Image data were acquired using a three-dimensional spoiled GRASS sequence, and brain images were reformatted in three planes. Temporal lobe structures including the amygdala, hippocampus, parahippocampus, and total temporal lobe were measured to obtain volumes for each structure in the three subject groups. Severity of symptoms in both patient groups was assessed at the time the magnetic resonance images were obtained.
      Results: Hippocampal volumes were significantly smaller in the schizophrenic group than in both bipolar and normal comparison subjects. Further, amygdala volumes were significantly larger in the bipolar group than in both schizophrenic and normal comparison subjects.
      Conclusions: The results suggest differences in affected limbic structures in patients with schizophrenia and bipolar disorder. These specific neuroanatomic abnormalities may shed light on the underlying pathophysiology and presentation of the two disorders.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Biological Psychiatry
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

      1. Aggleton J.P The Amygdala. Wiley-Liss, New York1992
        • Altshuler L.L
        • Bartzokis G
        • Grieder T
        • Curran J
        • Mintz J
        Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia.
        Arch Gen Psychiatry. 1998; 55: 663-664
        • Altshuler L.L
        • Casanova M.F
        • Goldberg T.E
        • Kleinman J.E
        The hippocampus and parahippocampus in schizophrenic, suicide, and control brains.
        Arch Gen Psychiatry. 1990; 47: 1029-1033
        • Altshuler L.L
        • Conrad A
        • Hauser P
        • Li X
        • Guze B
        • Denikoff K
        • et al.
        Reduction of temporal lobe volume in bipolar disorder.
        Arch Gen Psychiatry. 1991; 48: 482-483
        • Andreasen N.C
        The Scale for the Assessment of Negative Symptoms (SANS). The University of Iowa, Iowa City1984
        • Andreasen N.C
        The Scale for the Assessment of Positive Symptoms (SAPS). The University of Iowa, Iowa City1984
        • Andreasen N.C
        • Swayze II, V.W
        • Flaum M
        • Alliger R
        • Cohen G
        Ventricular abnormalities in affective disorder.
        Am J Psychiatry. 1990; 147: 893-900
        • Arnold S.E
        • Hyman B.T
        • Van Hoesen G.W
        • Damasio A.R
        Some cytoarchitectural abnormalities of the entorhinal cortex in schizophrenia.
        Arch Gen Psychiatry. 1991; 48: 625-632
        • Aylward E.H
        • Roberts-Twillie J.V
        • Barta P.E
        • Kumar A.J
        • Harris G.J
        • Geer M
        • et al.
        Basal ganglia volumes and white matter hyperintensities in patients with bipolar disorder.
        Am J Psychiatry. 1994; 151: 687-693
        • Barta P.E
        • Pearlson G.D
        • Powers R.E
        • Richards S.S
        • Tune L.E
        Auditory hallucinations and smaller superior temporal gyral volume in schizophrenia.
        Am J Psychiatry. 1990; 147: 1457-1462
        • Bartzokis G
        • Altshuler L.L
        • Grieder T
        • Curran J
        • Keen B
        • Dixon W.J
        Reliability of medial temporal lobe volume measurements using reformatted 3D images.
        Psychiatry Res. 1998; 82: 11-24
        • Bartzokis G
        • Mintz J
        • Marx P
        • Osborn D
        • Gutkind D
        • Chiang F
        • et al.
        Reliability of in vivo volume measures of hippocampus and other brain structures using MRI.
        Magn Reson Imaging. 1993; 11: 993-1006
        • Baxter L.R
        • Schwartz J.M
        • Phelps M.E
        • Mazziotta J.C
        • Guze B.H
        • Selin C.E
        • et al.
        Reduction of prefrontal cortex glucose metabolism common to three types of depression.
        Arch Gen Psychiatry. 1989; 46: 243-250
        • Becker T
        • Elmer K
        • Schneider F
        • Schneider M
        • Grodd W
        • Bartels M
        • et al.
        Confirmation of reduced temporal limbic structure volume on magnetic resonance imaging in male patients with schizophrenia.
        Psychiatry Res. 1996; 67: 135-143
      2. Ben-Ari Y The Amygdaloid Complex. Elsevier, Amsterdam1981
        • Bentson J
        • Reza M
        • Winter J
        • Wilson G
        Steroids and apparent cerebral atrophy on CT scans.
        J Comput Assist Tomogr. 1978; 2: 16-23
        • Bilder R.M
        • Bogerts B
        • Ashtari M
        • Wu H
        • Alvir J.M
        • Jody D
        • et al.
        Anterior hippocampal volume reductions predict frontal lobe dysfunction in first episode schizophrenia.
        Schizophr Res. 1995; 17: 47-58
        • Bogerts B
        • Ashtari M
        • Degreef G
        • Alvir J.M.J
        • Bilder R.M
        • Lieberman J.A
        Temporal limbic structure volumes on magnetic resonance images in first episode schizophrenia.
        Psychiatry Res Neuroimaging. 1990; 35: 1-13
        • Bogerts B
        • Falkai P
        • Haupts M
        • Greve B
        • Tapernon-Franz U
        • Heinzmann U
        Postmortem volume measurements of limbic system and basal ganglia structures in chronic schizophrenics.
        Schizophr Res. 1984; 3: 295-301
        • Bogerts B
        • Lieberman J.A
        • Ashtari M
        • Bilder R.M
        • Degreef G
        • Lerner G
        • et al.
        Hippocampus–amygdala volumes and psychopathology in chronic schizophrenia.
        Biol Psychiatry. 1993; 33: 236-246
        • Bogerts B
        • Meertz E
        • Schonfeldt-Bausch R
        Basal ganglia and limbic system pathology in schizophrenia.
        Arch Gen Psychiatry. 1985; 42: 784-791
        • Breier A
        • Buchanan R.W
        • Elkashef A
        • Munson R.C
        • Kirkpatrick B
        • Gellad F
        Brain morphology and schizophrenia.
        Arch Gen Psychiatry. 1992; 49: 921-926
        • Breiter H.C
        • Etcoff N.L
        • Whalen P.F
        • Kennedy W.A
        • Rauch S.L
        • Buckner R.L
        • et al.
        Response and habituation of the human amygdala during visual processing of facial expression.
        Neuron. 1996; 17: 875-887
        • Bremner J.D
        • Randall P
        • Scott T.M
        • Bronen R.A
        • Seibyl J.P
        • Southwick S.M
        • et al.
        MRI-based measurement of hippocampal volume in patients with combat-related posttraumatic stress disorder.
        Am J Psychiatry. 1995; 152: 973-981
        • Brothers L
        • Ring B
        • Kling A
        Response of neurons in the macaque amygdala to complex social stimuli.
        Behav Brain Res. 1990; 41: 199-213
        • Brown R
        • Colter N
        • Corsellis J.A
        • Crow T.J
        • Frith C.D
        • Jagoe R
        • et al.
        Postmortem evidence of structural brain changes in schizophrenia.
        Arch Gen Psychiatry. 1986; 43: 36-42
        • Buchanan R.W
        • Breier A
        • Kirpatrick B
        • Elkashet A
        • Munson R.C
        • Gellad F
        • Carpenter W.T
        Structural abnormalities in deficit and nondeficit schizophrenia.
        Am J Psychiatry. 1993; 150: 59-65
        • Chakos M.H
        • Liberman J.A
        • Alvir J
        • Bilder R.M
        • Ashtari M
        Caudate nuclei volumes in schizophrenic patients treated with typical antipsychotics or clozapine.
        Lancet. 1995; 345: 456-457
        • Chakos M.H
        • Liberman J.A
        • Bilder R.M
        • Borenstein M
        • Lerner G
        • Bogerts B
        • et al.
        Increase in caudate nuclei volumes of first-episode schizophrenia patients taking antipsychotic drugs.
        Am J Psychiatry. 1994; 151: 1430-1436
        • Christison G.W
        • Casanova M.F
        • Weinberger D.R
        • Rawlings R
        • Kleinman J.E
        A quantitative investigation of hippocampal pyramidal cell size, shape, and variability of orientation in schizophrenia.
        Arch Gen Psychiatry. 1989; 46: 1027-1032
        • Coffman J.A
        • Bornstein R.A
        • Olson S.C
        • Schwarzkopf S.B
        • Nasrallah H.A
        Cognitive impairment and cerebral structure by MRI in bipolar disorder.
        Biol Psychiatry. 1990; 27: 1188-1196
        • Cuenod C.A
        • Denys A
        • Michot J.L
        • Jehenson P
        • Forette F
        • Kaplan D
        • et al.
        Amygdala atrophy in Alzheimer’s disease.
        Arch Neurol. 1993; 50: 941-945
        • Dauphinais D
        • DeLisi L.E
        • Crow T.J
        • Alexandropolous K
        • Colter N
        • Tuma I
        • Gershon E.S
        Reduction in temporal lobe size in siblings with schizophrenia.
        Psychiatry Res Neuroimaging. 1990; 35: 137-147
        • DeLisi L.E
        • Hoff A.L
        • Schwartz J.E
        • Shields G.W
        • Halthorne S.N
        • Gupta S.M
        • et al.
        Brain morphology in first-episode schizophrenia-like psychotic patients.
        Biol Psychiatry. 1991; 29: 159-175
        • Drevets W.C
        • Price J.L
        • Simpson J.R
        • Todd R.D
        • Reich T
        • Vannier M
        • Ralchle M.E
        Subgenual prefrontal cortex abnormalities in mood disorders.
        Nature. 1997; 386: 824-827
        • Drevets W.C
        • Videen T.O
        • Price J.L
        • Preskorn S.H
        • Carmichael S.T
        • Raichle M.E
        A functional anatomical study of unipolar depression.
        Neuroscience. 1992; 12: 3628-3641
        • Dupont R.M
        • Jernigan T.L
        • Gillin J.C
        • Butters N
        • Delis D.C
        • Hesselink J.R
        Subcortical signal hyperintensities in bipolar patients detected by MRI (letter).
        Psychiatry Res. 1987; 21: 357-358
        • Dupont R.M
        • Jernigan T.L
        • Heindel W
        • Butters N
        • Shafer K
        • Wilson T
        • et al.
        Magnetic resonance imaging and mood disorders.
        Arch Gen Psychiatry. 1995; 52: 747-755
        • Elkashef A.M
        • Egan M.F
        • Frank J.A
        • Hyde T.M
        • Lewis B.K
        • Wyatt R.J
        Basal ganglia iron in tardive dyskinesia.
        Biol Psychiatry. 1994; 35: 16-21
        • Falkai P
        • Bogerts B
        Cell loss in the hippocampus of schizophrenics.
        Eur Arch Psychiatry Neurol Sci. 1986; 236: 154-161
        • Figiel G.S
        • Krishnan K.R.R
        • Rao V.P
        • Doraiswamy M
        • Ellinwood E.H
        • Nemeroff C.B
        • et al.
        Subcortical hyperintensities on brain magnetic resonance imaging.
        J Neuropsychiatry. 1991; 3: 18-22
      3. Flashman LA, Saykin AJ, Carrol KE, Bono DB, McAllister TW, Weaver JB, et al (1995, October): Relation of hippocampal and neocortical volumetry to functional MRI memory activation in patients with schizophrenia. Paper presented at the 10th annual meeting of the Society for Research in Psychopathology, Iowa City, Iowa.

        • Flaum M
        • Swayze II, V.W
        • O’Leary D.S
        • Yuh W.T.C
        • Ehrhardt J.C
        • Arndt S.V
        • Andreasen N.C
        Effects of diagnosis, laterality, and gender on brain morphology in schizophrenia.
        Am J Psychiatry. 1995; 152: 704-714
        • Frazier J.A
        • Giedd J.N
        • Kaysen D
        • Albus K
        • Hamburger S
        • Alaghband-Rad J
        • et al.
        Childhood-onset schizophrenia.
        Am J Psychiatry. 1996; 153: 564-566
        • Fukuzako H
        • Fukuzako T
        • Hashiguchi T
        • Hokazano Y
        • Takeuchi K
        • Hirakawa K
        • et al.
        Reduction in hippocampal formation volume is caused mainly by its shortening in chronic schizophrenia.
        Biol Psychiatry. 1996; 39: 938-945
        • Gilbertson M.W
        • van Kammen D.P
        Recent and remote memory dissociation.
        Biol Psychiatry. 1997; 42: 585-595
        • Gloor P
        • Olivier A
        • Quesney L.F
        • Andermann F
        • Horowitz S
        The role of the limbic system in experiential phenomena of temporal lobe epilepsy.
        Ann Neurol. 1982; 12: 129-144
        • Goldberg T.E
        • Torrey E.F
        • Berman K.F
        • Weinberger D.R
        Relations between neuropsychological performance and brain morphological and psychological measures in monozygotic twins discordant for schizophrenia.
        Psychiatry Res. 1994; 55: 51-61
        • Gur R.E
        • Cowell P
        • Turetsky B.I
        • Gallacher F
        • Cannon T
        • Bilker W
        • Gur R.C
        A follow-up magnetic resonance imaging study of schizophrenia.
        Arch Gen Psychiatry. 1998; 55: 145-152
        • Halgren E
        The amygdala contribution to emotion and memory.
        in: Ben-Ari Y The Amygdaloid Complex. Elsevier, Amsterdam1981: 395-408
        • Hamilton M
        A rating scale for depression.
        J Neurol Neurosurg Psychiatry. 1960; 12: 56-62
        • Harvey I
        • Persaud R
        • Ron M.A
        • Baker G
        • Murray R.M
        Volumetric MRI measurements in bipolars compared with schizophrenics and healthy controls.
        Psychol Med. 1994; 24: 689-699
        • Hauser P
        • Dauphinais I.D
        • Berrettini W
        • DeLisi L.E
        • Gelernter J
        • Post R.M
        Corpus callosum dimensions measured by magnetic resonance imaging in bipolar affective disorder and schizophrenia.
        Biol Psychiatry. 1989; 26: 659-668
        • Hauser P.H
        • Altshuler L.L
        • Berrettini W
        • Dauphinais I.D
        • Gelernter J
        • Post R.M
        Temporal lobe measurement in primary affective disorder by magnetic resonance imaging.
        J Neuropsychiatry Clin Neurosci. 1989; 1: 128-134
        • Heckers S
        • Heinsen H
        • Geiger B
        • Beckmann H
        Hippocampal neuron number in schizophrenia. A stereological study.
        Arch Gen Psychiatry. 1991; 48: 1002-1008
        • Heckers S
        • Heinsen Y
        • Beckman H
        Cortex, white matter, and basal ganglia in schizophrenia.
        Biol Psychiatry. 1991; 29: 556-566
        • Heimer L
        • Switzer R.D
        • Van Hoesen G.W
        Ventral striatum and ventral pallidum. Components of the motor system?.
        Trends Neurosci. 1982; 5: 83-87
        • Hirayasu V
        • Shenton M.E
        • Salisbury D.F
        • Dickey C.C
        • Fischer I.A
        • Mazzoni P
        • et al.
        Lower left temporal lobe MRI volumes in patients with first-episode schizophrenia compared with psychotic patients with first-episode affective disorder and normal subjects.
        Am J Psychiatry. 1998; 155: 1384-1391
        • Hokama H
        • Shenton M.E
        • Nestor P.G
        • Kikinis R
        • Levitt J
        • Metcalf D
        • et al.
        Caudate, putamen, and globus pallidus volume in schizophrenia.
        Psychiatry Res Neuroimaging. 1995; 61: 209-229
        • Jakob H
        • Beckman H
        Prenatal developmental disturbances in the limbic allocortex in schizophrenics.
        J Neural Transm. 1986; 65: 303-326
        • Jernigan T.L
        • Zisook S
        • Heaton R.K
        • Mornville J.T
        • Hesselink J.R
        • Braff D.L
        Magnetic resonance imaging abnormalities in lenticular nuclei and cerebral cortex in schizophrenia.
        Arch Gen Psychiatry. 1991; 48: 881-890
        • Jeste D.V
        • Lohr J.B
        Hippocampal pathologic findings in schizophrenia.
        Arch Gen Psychiatry. 1989; 46: 1019-1024
        • Johnstone E.C
        • Owens D.G
        • Crow T.J
        • Frith C.D
        • Alexandropolis K
        • Bydder G
        • Colter N
        Temporal lobe structure as determined by nuclear magnetic resonance in schizophrenia and bipolar affective disorder.
        J Neurol Neurosurg Psychiatry. 1989; 52: 736-741
        • Jurjus G.J
        • Nasrallah H.A
        • Brogan M
        • Olson S.C
        Developmental brain anomalies in schizophrenia and bipolar disorder.
        J Neuropsychiatry. 1993; 5: 375-378
        • Karaken D.A
        • Gur R.C
        • Mozley P.D
        • Mozley L.H
        • Saykin A.J
        • Shtasel D.L
        • Gur R.E
        Cognitive functioning and neuroanatomic volume measures in schizophrenia.
        Neuropsychology. 1995; 9: 211-219
        • Kato T
        • Shioiri T
        • Murashita J
        • Hamakawa H
        • Inubushi T
        • Takhashi S
        Phosphorus-31 magnetic resonance spectroscopy and ventricular enlargement in bipolar disorder.
        Psychiatry Res Neuroimaging. 1994; 55: 41-50
        • Kawasaki Y
        • Maeda Y
        • Urata K
        • Higashima M
        • Yamaguchi N
        • Suzuki M
        • et al.
        A quantitative magnetic resonance imaging study of patients with schizophrenia.
        Eur Arch Psychiatry Clin Neurosci. 1993; 242: 268-272
        • Kelsoe J.R
        • Cadet J.L
        • Pickar D
        • Weinberger D.R
        Quantitative neuroanatomy in schizophrenia.
        Arch Gen Psychiatry. 1988; 45: 533-541
        • Keshavan M.S
        • Bagwell W.W
        • Haas G.L
        • Sweeney J.A
        • Schoole N.R
        • Pettegrew J.W
        Changes in caudate volume with neuroleptic treatment.
        Lancet. 1994; 344: 1434
        • Kesslak J.P
        • Nalcioglu O
        • Cotman C.W
        Quantification of magnetic resonance scans for hippocampal and parahippocampal atrophy in Alzheimer’s disease.
        Neurology. 1991; 41: 51-54
        • Ketter T.A
        • Andreason P.J
        • George M.S
        • Lee C
        • Gill D.S
        • Parekh P.I
        • et al.
        Anterior paralimbic mediation of procaine-induced emotional and psychosensory experiences.
        Arch Gen Psychiatry. 1996; 53: 59-69
        • Killiany R.J
        • Moss M.B
        • Albert M.S
        • Sandor T
        • Tieman J
        • Jolesz F
        Temporal lobe regions on magnetic resonance imaging identify patients with early Alzheimer’s disease.
        Arch Neurol. 1993; 50: 949-954
        • Kling A.S
        • Tachiki K
        • Lloyd R
        Neurochemical correlates of the Kluver-Bucy syndrome by in vivo microdialysis in monkey.
        Behav Brain Res. 1993; 56: 161-170
        • Kovelman J.A
        • Scheibel A.B
        A neurohistological correlate of schizophrenia.
        Biol Psychiatry. 1984; 19: 1601-1621
        • LeDoux J.E
        Emotional memory systems in the brain.
        Behav Brain Res. 1993; 58: 69-79
        • Lewine R.J
        • Hudgins P
        • Brown F
        • Caudle J
        • Risch S.C
        Differences in qualitative brain morphology findings in schizophrenia, major depression, bipolar disorder and normal volunteers.
        Schizophr Res. 1995; 15: 253-259
        • McCarley R.W
        • Shenton M.E
        • O’Donnell B.F
        • Faux S.F
        • Kikinis R
        • Nestor P.G
        • Jolesz F.A
        Auditory P300 abnormalities and left posterior superior temporal gyrus volume reduction in schizophrenia.
        Arch Gen Psychiatry. 1993; 50: 190-197
        • McDonald W.M
        • Krishnan K.R.R
        • Doraiswamy P.M
        • Blazer D.G
        Occurrence of subcortical hyperintensities in elderly subjects with mania.
        Psychiatry Res Neuroimaging. 1991; 40: 211-220
        • Morris J.S
        • Frith C.D
        • Perrett D.I
        • Rowland D
        • Young A.W
        • Calder A.J
        • Dolan R.J
        A differential neural response in the human amygdala to fearful and happy facial expressions.
        Nature. 1996; 31: 812-814
        • Nasrallah H.A
        • McCalley-Whitters M
        • Jacoby C.G
        Cerebral ventricular enlargement in young manic males—a controlled CT study.
        J Affect Disord. 1982; 4: 15-19
        • Nauta W.J.H
        Fiber degeneration following lesions of the amygdaloid complex in the monkey.
        J Anat. 1961; 95: 515-531
        • Nauta W.J.H
        The problem of the frontal lobe.
        J Psychiatr Res. 1971; 8: 167-187
        • Nelson M.D
        • Saykin A.J
        • Flashman L.A
        • Riordan H.J
        Hippocampal volume reduction in schizophrenia as assessed by magnetic resonance imaging.
        Arch Gen Psychiatry. 1998; 55: 433-440
        • Norris S.D
        • Krishnan K.R
        • Ahearn E
        Structural changes in the brain of patients with bipolar affective disorder by MRI.
        Prog Neuropsychopharmacol Biol Psychiatry. 1997; 21: 1323-1337
        • Overall J.E
        The Brief Psychiatric Rating Scale (BPRS).
        Psychopharmacol Bull. 1988; 24: 97-99
        • Pearlson G.D
        • Barta P.E
        • Powers R.E
        • Menon R.R
        • Richards S.S
        • Aylward E.H
        • et al.
        Medial and superior temporal gyral volumes and cerebral asymmetry in schizophrenia versus bipolar disorder.
        Biol Psychiatry. 1997; 41: 1-14
        • Pearlson G.D
        • Garbacz D.J
        • Breakey W.R
        • Ahn H.S
        • DePaulo J.R
        Lateral ventricular enlargement associated with persistent unemployment and negative symptoms in both schizophrenia and bipolar disorder.
        Psychiatry Res. 1984; 12: 1-9
        • Pearlson G.D
        • Harris G.J
        • Powers R.E
        • Barta P.E
        • Camargo E.E
        • Chase G.A
        • et al.
        Quantitative changes in the mesial temporal volume, regional cerebral blood flow, and cognition in Alzheimer’s disease.
        Arch Gen Psychiatry. 1992; 49: 402-408
        • Pearlson G.D
        • Veroff A.E
        Computerized tomographic scan changes in manic-depressive illness.
        Lancet. 1981; 2: 470
        • Pribram K.H
        The hippocampal system and recombinant processing.
        in: Isaacson R.L Pribram K.H The Hippocampus. Plenum Press, New York1986: 329-370
        • Price J.L
        The efferent projections of the amygdaloid complex in the rat, cat and monkey.
        in: Ben-Ari Y The Amygdaloid Complex. Elsevier, Amsterdam1981: 121-132
        • Regier D.A
        • Farmer M.E
        • Rae D.S
        • Locke B.Z
        • Keith S.J
        • Judd L.L
        • Goodwin F.K
        Comorbidity of mental disorders with alcohol and other drug abuse.
        JAMA. 1990; 264: 2511-2518
        • Risch S.C
        • Lewine R.J
        • Kalin N.H
        • Jewart R.D
        • Risby E.D
        • Caudle J.M
        • et al.
        Limbic-hypothalamic-pituitary-adrenal axis activity and ventricular-to-brain ratio studies in affective illness and schizophrenia.
        Neuropsychopharmacology. 1992; 6: 95-100
        • Rolls E.T
        Neurophysiology and functions of the primate amygdala.
        in: Aggleton J.P The Amygdala. Wiley-Liss, New York1992: 143-165
        • Rossi A
        • Stratta P
        • Di Michele V
        • Gallucci M
        • Splendiani A
        • de Cataldo S
        • Casacchia M
        Temporal lobe structure by magnetic resonance in bipolar affective disorders and schizophrenia.
        J Affect Disord. 1991; 21: 19-22
        • Rossi A
        • Stratta P
        • Mancini F
        • Gallucci M
        • Mattei P
        • Core L
        • et al.
        Magnetic resonance imaging findings of amygdala-anterior hippocampus shrinkage in male patients with schizophrenia.
        Psychiatry Res. 1994; 52: 43-53
        • Roy P.D
        • Zipursky R.B
        • Saint-Cyr J.A
        • Bury A
        • Langevin R
        • Seeman M.V
        Temporal horn enlargement is present in schizophrenia and bipolar disorder.
        Biol Psychiatry. 1998; 44: 418-422
        • Saykin A.J
        • Gur R.C
        • Gur R.E
        • Mozley P.D
        • Mozley L.H
        • Resnick S.M
        • et al.
        Neuropsychological function in schizophrenia.
        Arch Gen Psychiatry. 1991; 48: 618-624
        • Saykin A.J
        • Shtasel D.L
        • Gur R.E
        • Kester D.B
        • Mozley L.H
        • Stafiniak P
        • Gur R.C
        Neuropsychological deficits in neuroleptic-naı̈ve, first episode schizophrenic patients.
        Arch Gen Psychiatry. 1994; 51: 124-131
        • Schlaepfer T.E
        • Harris G.J
        • Tien A.Y
        • Peng L.W
        • Lee S
        • Federman E
        • et al.
        Decreased regional cortical gray matter volume in schizophrenia.
        Am J Psychiatry. 1994; 151: 842-848
        • Schneider F
        • Grodd W
        • Weiss U
        • Klose U
        • Mayar K.R
        • Nagele T
        • Gur R.C
        Functional MRI reveals left amygdala activation during emotion.
        Psychiatry Res Neuroimaging. 1997; 76: 75-82
        • Seab J.P
        • Jagust W.J
        • Wong S.T.S
        • Roos M.S
        • Reed B.R
        • Budinger T.F
        Quantitative NMR measurements of hippocampal atrophy in Alzheimer’s disease.
        Magn Reson Med. 1988; 8: 200-208
        • Servan-Schreiber D
        • Perlstein W.M
        • Cohen J.D
        • Mintun M
        Selective pharmacological activation of limbic structures in human volunteers.
        J Neuropsychiatry Clin Neurosci. 1998; 10: 148-159
        • Shenton M.E
        • Kikinis R
        • Jolesz F.A
        • Pollak S.D
        • LeMay M
        • Wible C.G
        • et al.
        Abnormalities of the left temporal lobe and thought disorder in schizophrenia.
        N Engl J Med. 1992; 327: 604-612
        • Spitzer R.L
        • Williams J.B.W
        • Gibbon M
        • First M.B
        Structured Clinical Interview for DSM IV. New York State Psychiatric Institute, Biometrics Research Department, New York1994
        • Squillace K.M
        • Post R.M
        • Savard R
        • Erwin-Gorman M
        Life charting of the longitudinal course of affective illness.
        in: Post R.M Ballenger J.C Neurobiology of Mood Disorders. Williams & Williams, Baltimore1984
        • Strakowski S.M
        • DelBello M.P
        • Sax K.W
        • Zimmerman M.E
        • Shear P.K
        • Hawkins J.M
        • Larson E.R
        Brain magnetic resonance imaging of structural abnormalities in bipolar disorder.
        Arch Gen Psychiatry. 1999; 56: 254-260
        • Strakowski S.M
        • Wilson D.R
        • Tohen M
        • Woods B.T
        • Douglass A.W
        • Stoll A.L
        Structural brain abnormalities in mania at first hospitalization.
        Biol Psychiatry. 1993; 33: 602-609
        • Suddath R.L
        • Casanova M.F
        • Goldberg T.E
        • Daniel D.G
        • Kelsoe J.R
        • Weinberger D.R
        Temporal lobe pathology in schizophrenia.
        Am J Psychiatry. 1989; 146: 464-472
        • Suddath R.L
        • Christison G.W
        • Torrey B.F
        • Casanova M.F
        • Weinberger D.R
        Anatomical abnormalities in the brain of monozygotic twins discordant for schizophrenia.
        N Engl J Med. 1990; 322: 789-794
        • Swayze II, V.W
        • Andreasen N.C
        • Alliger R.J
        • Ehrhardt J.C
        • Yuh W.T.C
        Structural brain abnormalities in bipolar affective disorder.
        Arch Gen Psychiatry. 1990; 47: 1054-1059
        • Swayze II, V.W
        • Andreasen N.C
        • Alliger R.J
        • Yuh W.T.C
        • Ehrhardt J.C
        Subcortical and temporal structures in affective disorder and schizophrenia.
        Biol Psychiatry. 1992; 31: 221-240
        • Turetsky B.T
        • Cowell P.E
        • Gur R.C
        • Grossman R.I
        • Shtasel D.L
        • Gur R.E
        Frontal and temporal lobe brain volumes in schizophrenia.
        Arch Gen Psychiatry. 1995; 52: 1061-1070
        • Videbech P
        MRI findings in patients with affective disorder.
        Acta Psychiatr Scand. 1997; 96: 157-168
        • Weinberger D.R
        A connectionist approach to the prefrontal cortex.
        J Neuropsychiatry Clin Neurosci. 1993; 5: 241-253
        • Weinberger D.R
        • Berman K.F
        • Suddath R
        • Torrey E.F
        Evidence of dysfunction of a prefrontal-limbic network in schizophrenia.
        Am J Psychiatry. 1992; 149: 890-897
        • Weiskrantz L
        Behavioral changes associated with ablation of the amygdaloid complex in monkeys.
        J Comp Physiol Psychol. 1956; 49: 381-391
        • Woods B.T
        • Brennan S
        • Yurgelun-Todd D
        • Young T
        • Panzarino P
        MRI abnormalities in major psychiatric disorders.
        J Neuropsychiatry Clin Neurosci. 1995; 7: 49-53
        • Woods B.T
        • Yurgelun-Todd D
        • Mikulis D
        • Pillay S.S
        Age-related MRI abnormalities in bipolar illness.
        Biol Psychiatry. 1995; 38: 846-847
        • Young R.C
        • Biggs J.T
        • Ziegler V.E
        • Meyer D.A
        A rating scale for mania.
        Br J Psychiatry. 1978; 133: 429-435
        • Zipursky R.B
        • Marsh L
        • Lim K.O
        • DeMent S
        • Shear P.K
        • Sullivan E.V
        • et al.
        Volumetric MRI assessment of temporal lobe structures in schizophrenia.
        Biol Psychiatry. 1994; 35: 501-516