Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-22T05:39:50.395Z Has data issue: false hasContentIssue false

Schizophrenia as a progressive brain disease

Published online by Cambridge University Press:  16 April 2020

N.E.M. van Haren*
Affiliation:
Rudolf Magnus Institute of Neuroscience, Department of Psychiatry, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands
W. Cahn
Affiliation:
Rudolf Magnus Institute of Neuroscience, Department of Psychiatry, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands
H.E. Hulshoff Pol
Affiliation:
Rudolf Magnus Institute of Neuroscience, Department of Psychiatry, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands
R.S. Kahn
Affiliation:
Rudolf Magnus Institute of Neuroscience, Department of Psychiatry, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands
*
Corresponding author. Department of Psychiatry, A.01.126, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands. Tel.: +31 30 2507130; fax: +31 30 2505443. E-mail address: [email protected] (N.E.M. van Haren).
Get access

Abstract

There is convincing evidence that schizophrenia is characterized by abnormalities in brain volume. At the Department of Psychiatry of the University Medical Centre Utrecht, Netherlands, we have been carrying out neuroimaging studies in schizophrenia since 1995. We focused our research on three main questions. First, are brain volume abnormalities static or progressive in nature? Secondly, can brain volume abnormalities in schizophrenia be explained (in part) by genetic influences? Finally, what environmental factors are associated with the brain volume abnormalities in schizophrenia?

Based on our findings we suggest that schizophrenia is a progressive brain disease. We showed different age-related trajectories of brain tissue loss suggesting that brain maturation that occurs in the third and fourth decade of life is abnormal in schizophrenia. Moreover, brain volume has been shown to be a useful phenotype for studying schizophrenia. Brain volume is highly heritable and twin and family studies show that unaffected relatives show abnormalities that are similar, but usually present to a lesser extent, to those found in the patients. However, also environmental factors play a role. Medication intake is indeed a confounding factor when interpreting brain volume (change) abnormalities, while independent of antipsychotic medication intake brain volume abnormalities appear influenced by the outcome of the illness.

In conclusion, schizophrenia can be considered as a progressive brain disease with brain volume abnormalities that are for a large part influenced by genetic factors. Whether the progressive volume change is also mediated by genes awaits the results of longitudinal twin analyses. One of the main challenges for the coming years, however, will be the search for gene-by-environment interactions on the progressive brain changes in schizophrenia.

Type
Original article
Copyright
Copyright © European Psychiatric Association 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Agartz, I.Sedvall, G.C.Terenius, L.Kulle, B.Frigessi, A.Hall, H.et al.BDNF gene variants and brain morphology in schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2006 Jul 5;141(5):513523.CrossRefGoogle Scholar
American Psychiatric Association, Diagnostic and statistical manual of mental disorders (DSM-IV). 4th edWashington DC: American Psychiatric Association; 1994.Google Scholar
Arango, C.Breier, A.McMahon, R.Carpenter, W.T. Jr.Buchanan, R.W.The relationship of clozapine and haloperidol treatment response to prefrontal, hippocampal, and caudate brain volumes. Am J Psychiatry 2003 Aug;160(8):14211427.CrossRefGoogle ScholarPubMed
Ashburner, J.Friston, K.J.Voxel-based morphometry–the methods. Neuroimage 2000 Jun;11(6 Pt 1):805821.CrossRefGoogle Scholar
Ashburner, J.Friston, K.J.Why voxel-based morphometry should be used. Neuroimage 2001 Dec;14(6):12381243.CrossRefGoogle ScholarPubMed
Baare, W.F.Hulshoff Pol, H.E.Boomsma, D.I.Posthuma, D.De Geus, E.J.Schnack, H.G.et al.Quantitative genetic modeling of variation in human brain morphology. Cereb Cortex 2001 Sep;11(9):816824.CrossRefGoogle ScholarPubMed
Baare, W.F.van Oel, C.J.Hulshoff Pol, H.E.Schnack, H.G.Durston, S.Sitskoorn, M.M.et al.Volumes of brain structures in twins discordant for schizophrenia. Arch Gen Psychiatry 2001 Jan;58(1):3340.CrossRefGoogle Scholar
Block, R.I.O'Leary, D.S.Ehrhardt, J.C.Augustinack, J.C.Ghoneim, M.M.Arndt, S.et al.Effects of frequent marijuana use on brain tissue volume and composition. Neuroreport 2000 Feb 28;113491496.CrossRefGoogle ScholarPubMed
Bookstein, F.L.“Voxel-based morphometry” should not be used with imperfectly registered images. Neuroimage 2001 Dec;14(6):14541462.CrossRefGoogle Scholar
Boos, H.B.Aleman, A.Cahn, W.Pol, H.H.Kahn, R.S.Brain volumes in relatives of patients with schizophrenia: a meta-analysis. Arch Gen Psychiatry 2007 Mar;64(3):297304.CrossRefGoogle ScholarPubMed
Breier, A.Schreiber, J.L.Dyer, J.Pickar, D.National Institute of Mental Health longitudinal study of chronic schizophrenia. Prognosis and predictors of outcome. Arch Gen Psychiatry 1991 Mar;48(3):239246.CrossRefGoogle ScholarPubMed
Brickman, A.M.Buchsbaum, M.S.Ivanov, Z.Borod, J.C.Foldi, N.S.Hahn, E.et al.Internal capsule size in good-outcome and poor-outcome schizophrenia. J Neuropsychiatry Clin Neurosci 2006;18(3):364376.CrossRefGoogle ScholarPubMed
Buchsbaum, M.S.Shihabuddin, L.Brickman, A.M.Miozzo, R.Prikryl, R.Shaw, R.et al.Caudate and putamen volumes in good and poor outcome patients with schizophrenia. Schizophr Res 2003 Nov 1;6415362.CrossRefGoogle ScholarPubMed
Buchsbaum, M.S.Someya, T.Teng, C.Y.Abel, L.Chin, S.Najafi, A.et al.PET and MRI of the thalamus in never-medicated patients with schizophrenia. Am J Psychiatry 1996 Feb;153(2):191199.Google ScholarPubMed
Buckholtz, J.W.Meyer-Lindenberg, A.Honea, R.A.Straub, R.E.Pezawas, L.Egan, M.F.et al.Allelic variation in RGS4 impacts functional and structural connectivity in the human brain. J Neurosci 2007 Feb 14;27715841593.CrossRefGoogle ScholarPubMed
Cahn, W.Hulshoff Pol, H.E.Bongers, M.Schnack, H.G.Mandl, R.C.van Haren, N.E.et al.Brain morphology in antipsychotic-naive schizophrenia: a study of multiple brain structures. Br J Psychiatry 2002 Sep;43 s66s72.CrossRefGoogle ScholarPubMed
Cahn, W.Hulshoff Pol, H.E.Caspers, E.van Haren, N.E.Schnack, H.G.Kahn, R.S.Cannabis and brain morphology in recent-onset schizophrenia. Schizophr Res 2004 Apr 1;672–3305307.CrossRefGoogle ScholarPubMed
Cahn, W.Hulshoff Pol, H.E.Lems, E.B.van Haren, N.E.Schnack, H.G.Van Der Linden, J.A.et al.Brain volume changes in first-episode schizophrenia: a 1-year follow-up study. Arch Gen Psychiatry 2002 Nov;59(11):10021010.CrossRefGoogle ScholarPubMed
Cahn, W.van Haren, N.E.Hulshoff Pol, H.E.Schnack, H.G.Caspers, E.Laponder, D.A.et al.Brain volume changes in the first year of illness and 5-year outcome of schizophrenia. Br J Psychiatry 2006 Oct;189 381382.CrossRefGoogle ScholarPubMed
Callicott, J.H.Straub, R.E.Pezawas, L.Egan, M.F.Mattay, V.S.Hariri, A.R.et al.Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. Proc Natl Acad Sci U S A 2005 Jun 14;1022486278632.CrossRefGoogle ScholarPubMed
Cannon, T.D.Mednick, S.A.Parnas, J.Schulsinger, F.Praestholm, J.Vestergaard, A.Developmental brain abnormalities in the offspring of schizophrenic mothers. II. Structural brain characteristics of schizophrenia and schizotypal personality disorder. Arch Gen Psychiatry 1994 Dec;51(12):955962.CrossRefGoogle ScholarPubMed
Cannon, T.D.Thompson, P.M.van Erp, T.G.Toga, A.W.Poutanen, V.P.Huttunen, M.et al.Cortex mapping reveals regionally specific patterns of genetic and disease-specific gray-matter deficits in twins discordant for schizophrenia. Proc Natl Acad Sci U S A 2002 Mar 5;99(5):32283233.CrossRefGoogle Scholar
Cannon, T.D.van Erp, T.G.Huttunen, M.Lonnqvist, J.Salonen, O.Valanne, L.et al.Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls. Arch Gen Psychiatry 1998 Dec;55(12):10841091.CrossRefGoogle ScholarPubMed
Carpenter, W.T. Jr.Buchanan, R.W.Schizophrenia. N Engl J Med 1994 Mar 10;330(10):681690.CrossRefGoogle ScholarPubMed
Chakos, M.H.Lieberman, J.A.Alvir, J.Bilder, R.Ashtari, M.Caudate nuclei volumes in schizophrenic patients treated with typical antipsychotics or clozapine. Lancet 1995 Feb 18;3458947456457.CrossRefGoogle ScholarPubMed
Chakos, M.H.Lieberman, J.A.Bilder, R.M.Borenstein, M.Lerner, G.Bogerts, B.et al.Increase in caudate nuclei volumes of first-episode schizophrenic patients taking antipsychotic drugs. Am J Psychiatry 1994 Oct;151(10):14301436.Google ScholarPubMed
Davidson, L.McGlashan, T.H.The varied outcomes of schizophrenia. Can J Psychiatry 1997 Feb;42(1):3443.CrossRefGoogle ScholarPubMed
Davis, K.L.Buchsbaum, M.S.Shihabuddin, L.Spiegel-Cohen, J.Metzger, M.Frecska, E.et al.. Ventricular enlargement in poor-outcome schizophrenia. [see comments]Biol Psychiatry 1998 Jun 1;4311783793.Google ScholarPubMed
Dazzan, P.Morgan, K.D.Orr, K.Hutchinson, G.Chitnis, X.Suckling, J.et al.Different effects of typical and atypical antipsychotics on grey matter in first episode psychosis: the AESOP study. Neuropsychopharmacology 2005;30:765774.CrossRefGoogle ScholarPubMed
Dean, B.Sundram, S.Bradbury, R.Scarr, E.Copolov, D.Studies on [3H]CP-55940 binding in the human central nervous system: regional specific changes in density of cannabinoid-1 receptors associated with schizophrenia and cannabis use. Neuroscience 2001;103(1):915.CrossRefGoogle Scholar
Degreef, G.Ashtari, M.Wu, H.W.Borenstein, M.Geisler, S.Lieberman, J.Follow up MRI study in first episode schizophrenia. Schizophr Res 1991 Oct;5(3):204206.CrossRefGoogle ScholarPubMed
DeLisi, L.E.Defining the course of brain structural change and plasticity in schizophrenia. Psychiatry Res 1999 Nov 8;92119.CrossRefGoogle Scholar
DeLisi, L.E.The significance of age of onset for schizophrenia. Schizophr Bull 1992;18(2):209215.CrossRefGoogle Scholar
DeLisi, L.E.Goldin, L.R.Hamovit, J.R.Maxwell, M.E.Kurtz, D.Gershon, E.S.A family study of the association of increased ventricular size with schizophrenia. Arch Gen Psychiatry 1986 Feb;43(2):148153.CrossRefGoogle ScholarPubMed
DeLisi, L.E.Sakuma, M.Maurizio, A.M.Relja, M.Hoff, A.L.Cerebral ventricular change over the first 10 years after the onset of schizophrenia. Psychiatry Res 2004 Jan 15;130(1):5770.CrossRefGoogle ScholarPubMed
DeLisi, L.E.Sakuma, M.Tew, W.Kushner, M.Hoff, A.L.Grimson, R.Schizophrenia as a chronic active brain process: a study of progressive brain structural change subsequent to the onset of schizophrenia. Psychiatry Res 1997 Jul 4;74(3):129140.CrossRefGoogle ScholarPubMed
DeLisi, L.E.Stritzke, P.Riordan, H.Holan, V.Boccio, A.Kushner, M.et al.The timing of brain morphological changes in schizophrenia and their relationship to clinical outcome. [published erratum appears in Biol Psychiatry 1992 Jun 1;31(11):1172] Biol Psychiatry 1992 Feb 1 31(3):241254.Google ScholarPubMed
DeLisi, L.E.Tew, W.Xie, S.Hoff, A.L.Sakuma, M.Kushner, M.et al.A prospective follow-up study of brain morphology and cognition in first-episode schizophrenic patients: preliminary findings. Biol Psychiatry 1995 Sep 15;38(6):349360.CrossRefGoogle ScholarPubMed
Eaton, W.W.Bilker, W.Haro, J.M.Herrman, H.Mortensen, P.B.Freeman, H.et al.Long-term course of hospitalization for schizophrenia, part II: change with passage of time. Schizophr Bull 1992;18(2):229241.CrossRefGoogle ScholarPubMed
Eaton, W.W.Mortensen, P.B.Herrman, H.Freeman, H.Bilker, W.Burgess, P.et al.Long-term course of hospitalization for schizophrenia, part I: risk for rehospitalization. Schizophr Bull 1992;18(2):217228.CrossRefGoogle ScholarPubMed
van Erp, T.G.Saleh, P.A.Huttunen, M.Lonnqvist, J.Kaprio, J.Salonen, O.et al.Hippocampal volumes in schizophrenic twins. Arch Gen Psychiatry 2004 Apr;61(4):346353.CrossRefGoogle ScholarPubMed
van Erp, T.G.Saleh, P.A.Rosso, I.M.Huttunen, M.Lonnqvist, J.Pirkola, T.et al.Contributions of genetic risk and fetal hypoxia to hippocampal volume in patients with schizophrenia or schizoaffective disorder, their unaffected siblings, and healthy unrelated volunteers. Am J Psychiatry 2002 Sep;159(9):15141520.CrossRefGoogle ScholarPubMed
Ettinger, U.Picchioni, M.Landau, S.Matsumoto, K.van Haren, N.E.Marshall, N.et al.Magnetic resonance imaging of the thalamus and adhesio interthalamica in twins with schizophrenia. Arch Gen Psychiatry 2007 Apr;64(4):401409.CrossRefGoogle ScholarPubMed
Fenton, W.S.McGlashan, T.H.Natural history of schizophrenia subtypes. II. Positive and negative symptoms and long-term course. Arch Gen Psychiatry 1991 Nov;48(11):978986.CrossRefGoogle ScholarPubMed
Galderisi, S.Vita, A.Rossi, A.Stratta, P.Leonardi, M.Maj, M.et al.Qualitative MRI findings in patients with schizophrenia: a controlled study. Psychiatry Res 2000 Apr 10;98(2):117126.CrossRefGoogle ScholarPubMed
Giedd, J.N.Blumenthal, J.Jeffries, N.O.Castellanos, F.X.Liu, H.Zijdenbos, A.et al.Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 1999 Oct;2(10):861863.CrossRefGoogle ScholarPubMed
Gogate, N.Giedd, J.Janson, K.Rapoport, J.L.Brain imaging in normal and abnormal brain development: new perspectives for child psychiatry. Clin Neurosci Res 2001;1:283290.CrossRefGoogle Scholar
Gottesman, IISchizophrenia genesis – the origins of madness. New York: W.H. Freeman and Company; 1991.Google Scholar
Gur, R.E.Cowell, P.Turetsky, B.I.Gallacher, F.Cannon, T.Bilker, W.et al.A follow-up magnetic resonance imaging study of schizophrenia. Relationship of neuroanatomical changes to clinical and neurobehavioral measures. Arch Gen Psychiatry 1998 Feb;55(2):145152.CrossRefGoogle ScholarPubMed
Gur, R.E.Cowell, P.E.Latshaw, A.Turetsky, B.I.Grossman, R.I.Arnold, S.E.et al.Reduced dorsal and orbital prefrontal gray matter volumes in schizophrenia. Arch Gen Psychiatry 2000 Aug;57(8):761768.CrossRefGoogle Scholar
Gur, R.E.Maany, V.Mozley, P.D.Swanson, C.Bilker, W.Gur, R.C.Subcortical MRI volumes in neuroleptic-naive and treated patients with schizophrenia. [see comments]Am J Psychiatry 1998 Dec;155(12):17111717.CrossRefGoogle ScholarPubMed
Gur, R.E.Turetsky, B.I.Cowell, P.E.Finkelman, C.Maany, V.Grossman, R.I.et al.Temporolimbic volume reductions in schizophrenia. Arch Gen Psychiatry 2000 Aug;57(8):769775.CrossRefGoogle Scholar
Gurling, H.M.Critchley, H.Datta, S.R.McQuillin, A.Blaveri, E.Thirumalai, S.et al.Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Arch Gen Psychiatry 2006 Aug;63(8):844854.CrossRefGoogle Scholar
Harding, C.M.Course types in schizophrenia: an analysis of European and American studies. Schizophr Bull 1988;14(4):633643.CrossRefGoogle ScholarPubMed
van Haren, N.E.Cahn, W.Hulshoff Pol, H.E.Schnack, H.G.Caspers, E.Lemstra, A.et al.Brain volumes as predictor of outcome in recent-onset schizophrenia: a multi-center MRI study. Schizophr Res 2003 Nov 1;64(1);4152.CrossRefGoogle ScholarPubMed
van Haren, N.E.Hulshoff Pol, H.E.Schnack, H.G.Cahn, W.Brans, R.G.Carati, I.et al.Progressive brain volume decrease across the course of the illness in schizophrenia: a 5-year follow-up MRI study. Biol Psychiatry 63 2008 Jan 1;(1):106113.CrossRefGoogle Scholar
van Haren, N.E.Hulshoff Pol, H.E.Schnack, H.G.Cahn, W.Mandl, R.C.Collins, D.L.et al.Focal gray matter changes in schizophrenia across the course of the illness: a 5-year follow-up study. Neuropsychopharmacology 2008 Apr;18(4):312315.Google Scholar
van Haren, N.E.Picchioni, M.M.McDonald, C.Marshall, N.Davis, N.Ribchester, T.et al.A controlled study of brain structure in monozygotic twins concordant and discordant for schizophrenia. Biol Psychiatry 2004 Sep 15;56(6):454461.CrossRefGoogle Scholar
Harrison, P.J.The neuropathology of schizophrenia. A critical review of the data and their interpretation. Brain 1999 Apr;122(Pt 4):593624.CrossRefGoogle ScholarPubMed
Haug, J.O.Pneumoencephalographic studies in mental disease. Acta Psychiatr Scand 1962;38(Suppl. 165):1104.Google ScholarPubMed
Hirayasu, Y.Shenton, M.E.Salisbury, D.F.Frumin, M.Fischer, I.A.Farrell, D.et al.Progressive change in posterior superior temporal gyrus in schizophrenia. Biol Psychiatry 1999;45:S117 Ref type: abstractGoogle Scholar
Ho, B.C.Andreasen, N.C.Nopoulos, P.Arndt, S.Magnotta, V.Flaum, M.Progressive structural brain abnormalities and their relationship to clinical outcome: a longitudinal magnetic resonance imaging study early in schizophrenia. Arch Gen PsychiatryJun 2003;60(6):585594.CrossRefGoogle Scholar
Ho, B.C.Milev, P.O'Leary, D.S.Librant, A.Andreasen, N.C.Wassink, T.H.Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers. Arch Gen Psychiatry 2006 Jul;63(7):731740.CrossRefGoogle ScholarPubMed
Ho, B.C.Wassink, T.H.O'Leary, D.S.Sheffield, V.C.Andreasen, N.C.Catechol-O-methyl transferase Val(158)Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow. Mol Psychiatry 2005 Mar;10(3):229.CrossRefGoogle ScholarPubMed
Hoffman, W.F.Ballard, L.Turner, E.H.Casey, D.E.Three-year follow-up of older schizophrenics: extrapyramidal syndromes, psychiatric symptoms, and ventricular brain ratio. Biol Psychiatry 1991 Nov 1;309913926.CrossRefGoogle ScholarPubMed
Hulshoff Pol, H.E.Brans, R.G.van Haren, N.E.Schnack, H.G.Langen, M.Baare, W.F.et al.Gray and white matter volume abnormalities in monozygotic and same-gender dizygotic twins discordant for schizophrenia. Biol Psychiatry 2004 Jan 15;55(2):126130.CrossRefGoogle Scholar
Hulshoff Pol, H.E.Schnack, H.G.Bertens, M.G.van Haren, N.E.van der Tweel, I.Staal, W.G.et al.Volume changes in gray matter in patients with schizophrenia. Am J Psychiatry 2002 Feb;159(2):244250.CrossRefGoogle ScholarPubMed
Hulshoff Pol, H.E.Schnack, H.G.Mandl, R.C.Cahn, W.Collins, D.L.Evans, A.C.et al.Focal white matter density changes in schizophrenia: reduced inter-hemispheric connectivity. Neuroimage 2004 Jan;21(1):2735.CrossRefGoogle ScholarPubMed
Hulshoff Pol, H.E.Schnack, H.G.Mandl, R.C.van Haren, N.E.Koning, H.Collins, D.L.et al.Focal gray matter density changes in schizophrenia. Arch Gen Psychiatry 2001 Dec;58(12):11181125.CrossRefGoogle Scholar
Illowsky, B.P.Juliano, D.M.Bigelow, L.B.Weinberger, D.R.Stability of CT scan findings in schizophrenia: results of an 8 year follow-up study. J Neurol Neurosurg Psychiatry 1988 Feb;51(2):209213.CrossRefGoogle ScholarPubMed
Ingraham, L.J.Kety, S.S.Adoption studies of schizophrenia. Am J Med Genet 2000;97(1):1822.3.0.CO;2-L>CrossRefGoogle ScholarPubMed
Jaskiw, G.E.Juliano, D.M.Goldberg, T.E.Hertzman, M.Urow-Hamell, E.Weinberger, D.R.Cerebral ventricular enlargement in schizophreniform disorder does not progress. A seven year follow-up study. Schizophr Res 1994 Dec;14(1):2328.CrossRefGoogle Scholar
Johnstone, E.C.Crow, T.J.Frith, C.D.Husband, J.Kreel, L.Cerebral ventricular size and cognitive impairment in chronic schizophrenia. Lancet 1976 Oct 30;2(7992):924926.CrossRefGoogle ScholarPubMed
Joyal, C.C.Laakso, M.P.Tiihonen, J.Syvalahti, E.Vilkman, H.Laakso, A.et al.A volumetric MRI study of the entorhinal cortex in first episode neuroleptic-naive schizophrenia. Biol Psychiatry 2002 Jun 15;51(12):10051007.CrossRefGoogle ScholarPubMed
Joyal, C.C.Laakso, M.P.Tiihonen, J.Syvalahti, E.Vilkman, H.Laakso, A.et al.The amygdala and schizophrenia: a volumetric magnetic resonance imaging study in first-episode, neuroleptic-naive patients. Biol Psychiatry 54112003 Dec 1 13021304.CrossRefGoogle Scholar
Kasai, K.Shenton, M.E.Salisbury, D.F.Hirayasu, Y.Lee, C.U.Ciszewski, A.A.et al.Progressive decrease of left superior temporal gyrus gray matter volume in patients with first-episode schizophrenia. Am J Psychiatry 2003 Jan;160(1):156164.CrossRefGoogle ScholarPubMed
Kasai, K.Shenton, M.E.Salisbury, D.F.Hirayasu, Y.Onitsuka, T.Spencer, M.H.et al.Progressive decrease of left Heschl gyrus and planum temporale gray matter volume in first-episode schizophrenia: a longitudinal magnetic resonance imaging study. Arch Gen Psychiatry 2003 Aug;60(8):766775.CrossRefGoogle ScholarPubMed
Keller, A.Castellanos, F.X.Vaituzis, A.C.Jeffries, N.O.Giedd, J.N.Rapoport, J.L.Progressive loss of cerebellar volume in childhood-onset schizophrenia. Am J Psychiatry 2003 Jan;160(1):128133.CrossRefGoogle ScholarPubMed
Kemali, D.Maj, M.Galderisi, S.Milici, N.Salvati, A.Ventricle-to-brain ratio in schizophrenia: a controlled follow-up study. Biol Psychiatry 1989 Nov;26(7):756759.CrossRefGoogle ScholarPubMed
Kendler, K.S.Diehl, S.R.The genetics of schizophrenia: a current, genetic-epidemiologic perspective. Schizophr Bull 1993;19(2):261285.CrossRefGoogle ScholarPubMed
Keshavan, M.S.Bagwell, W.W.Haas, G.L.Sweeney, J.A.Schooler, N.R.Pettegrew, J.W.Changes in caudate volume with neuroleptic treatment. [letter]Lancet 1994 Nov 19;344(8934):1434.CrossRefGoogle ScholarPubMed
Keshavan, M.S.Diwadkar, V.A.Harenski, K.Rosenberg, D.R.Sweeney, J.A.Pettegrew, J.W.Abnormalities of the corpus callosum in first episode, treatment naive schizophrenia. J Neurol Neurosurg Psychiatry 2002 Jun;72(6):757760.CrossRefGoogle ScholarPubMed
Keshavan, M.S.Haas, G.L.Kahn, C.E.Aguilar, E.Dick, E.L.Schooler, N.R.et al.Superior temporal gyrus and the course of early schizophrenia: progressive, static, or reversible? J Psychiatr Res 1998 May;32(3–4):161167.CrossRefGoogle ScholarPubMed
Keshavan, M.S.Rosenberg, D.Sweeney, J.A.Pettegrew, J.W.Decreased caudate volume in neuroleptic-naive psychotic patients. Am J Psychiatry 1998 Jun;155(6):774778.Google ScholarPubMed
Laakso, M.P.Tiihonen, J.Syvalahti, E.Vilkman, H.Laakso, A.Alakare, B.et al.A morphometric MRI study of the hippocampus in first-episode, neuroleptic-naive schizophrenia. Schizophr Res 2001 May 30;50(1–2):37.CrossRefGoogle ScholarPubMed
Lawrie, S.M.Whalley, H.Kestelman, J.N.Abukmeil, S.S.Byrne, M.Hodges, A.et al.Magnetic resonance imaging of brain in people at high risk of developing schizophrenia. Lancet 1999 Jan 2;353(9146):3033.CrossRefGoogle ScholarPubMed
Lieberman, J.A.Is schizophrenia a neurodegenerative disorder? A clinical and neurobiological perspective. Biol Psychiatry 1999 Sep 15;46(6):729739.CrossRefGoogle ScholarPubMed
Lieberman, J.A.Chakos, M.Wu, H.Alvir, J.Hoffman, E.Robinson, D.et al.Longitudinal study of brain morphology in first episode schizophrenia. Biol Psychiatry 2001 Mar 15;49(6):487499.CrossRefGoogle ScholarPubMed
Lieberman, J.A.Tollefson, G.D.Charles, C.Zipursky, R.Sharma, T.Kahn, R.S.et al.Antipsychotic drug effects on brain morphology in first-episode psychosis. Arch Gen Psychiatry 2005 Apr;62(4):361370.CrossRefGoogle ScholarPubMed
Mathalon, D.H.Sullivan, E.V.Lim, K.O.Pfefferbaum, A.Progressive brain volume changes and the clinical course of schizophrenia in men: a longitudinal magnetic resonance imaging study. Arch Gen Psychiatry 2001 Feb;58(2):148157.CrossRefGoogle ScholarPubMed
McGlashan, T.H.A selective review of recent North American long-term follow-up studies of schizophrenia. Schizophr Bull 1988;14(4):515542.CrossRefGoogle ScholarPubMed
McIntosh, A.M.Baig, B.J.Hall, J.Job, D.Whalley, H.C.Lymer, G.K.et al.Relationship of catechol-O-methyltransferase variants to brain structure and function in a population at high risk of psychosis. Biol Psychiatry 2007 May 15;61(10):11271134.CrossRefGoogle Scholar
Mitelman, S.A.Newmark, R.E.Torosjan, Y.Chu, K.W.Brickman, A.M.Haznedar, M.M.et al.White matter fractional anisotropy and outcome in schizophrenia. Schizophr Res 2006 Oct;87(1–3):138159.CrossRefGoogle Scholar
Mitelman, S.A.Shihabuddin, L.Brickman, A.M.Hazlett, E.A.Buchsbaum, M.S.MRI assessment of gray and white matter distribution in Brodmann's areas of the cortex in patients with schizophrenia with good and poor outcomes. Am J Psychiatry 2003 Dec;160(12):21542168.CrossRefGoogle ScholarPubMed
Mitelman, S.A.Shihabuddin, L.Brickman, A.M.Hazlett, E.A.Buchsbaum, M.S.Volume of the cingulate and outcome in schizophrenia. Schizophr Res 2005 Jan 1;72(2–3):91108.CrossRefGoogle Scholar
Narr, K.L.Cannon, T.D.Woods, R.P.Thompson, P.M.Kim, S.Asunction, D.et al.Genetic contributions to altered callosal morphology in schizophrenia. J Neurosci 2002 May 1;22(9):37203729.CrossRefGoogle Scholar
Narr, K.L.van Erp, T.G.Cannon, T.D.Woods, R.P.Thompson, P.M.Jang, S.et al.A twin study of genetic contributions to hippocampal morphology in schizophrenia. Neurobiol Dis 2002 Oct;11(1):8395.CrossRefGoogle Scholar
Nasrallah, H.A.Olson, S.C.McCalley-Whitters, M.Chapman, S.Jacoby, C.G.Cerebral ventricular enlargement in schizophrenia. A preliminary follow-up study. Arch Gen Psychiatry 1986 Feb;43(2):157159.CrossRefGoogle ScholarPubMed
Nelson, M.D.Saykin, A.J.Flashman, L.A.Riordan, H.J.Hippocampal volume reduction in schizophrenia as assessed by magnetic resonance imaging: a meta-analytic study. [see comments]Arch Gen Psychiatry 1998 May;55(5):433440.CrossRefGoogle ScholarPubMed
Noga, J.T.Bartley, A.J.Jones, D.W.Torrey, E.F.Weinberger, D.R.Cortical gyral anatomy and gross brain dimensions in monozygotic twins discordant for schizophrenia. Schizophr Res 1996 Oct 18;22(1):2740.CrossRefGoogle Scholar
Ohnishi, T.Hashimoto, R.Mori, T.Nemoto, K.Moriguchi, Y.Iida, H.et al.The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia. Brain 2006 Feb;129(Pt 2):399410.CrossRefGoogle ScholarPubMed
van Os, J.Fahy, T.A.Jones, P.Harvey, I.Lewis, S.Williams, M.et al.Increased intracerebral cerebrospinal fluid spaces predict unemployment and negative symptoms in psychotic illness. A prospective study. Br J Psychiatry 1995 Jun;166(6):750758.CrossRefGoogle ScholarPubMed
Pantelis, C.Yucel, M.Wood, S.J.Velakoulis, D.Sun, D.Berger, G.et al.Structural brain imaging evidence for multiple pathological processes at different stages of brain development in schizophrenia. Schizophr Bull 2005 Jul;31(3):672696.CrossRefGoogle Scholar
Papiol, S.Molina, V.Desco, M.Rosa, A.Reig, S.Gispert, J.D.et al.Ventricular enlargement in schizophrenia is associated with a genetic polymorphism at the interleukin-1 receptor antagonist gene. Neuroimage 2005 Oct 1;27(4):10021006.CrossRefGoogle ScholarPubMed
Prasad, K.M.Patel, A.R.Muddasani, S.Sweeney, J.Keshavan, M.S.The entorhinal cortex in first-episode psychotic disorders: a structural magnetic resonance imaging study. Am J Psychiatry 2004 Sep;161(9):16121619.CrossRefGoogle ScholarPubMed
Prasad, K.M.Rohm, B.R.Keshavan, M.S.Parahippocampal gyrus in first episode psychotic disorders: a structural magnetic resonance imaging study. Prog Neuropsychopharmacol Biol Psychiatry 2004 Jul;28(4):651658.CrossRefGoogle ScholarPubMed
Puri, B.K.Hutton, S.B.Saeed, N.Oatridge, A.Hajnal, J.V.Duncan, L.et al.A serial longitudinal quantitative MRI study of cerebral changes in first-episode schizophrenia using image segmentation and subvoxel registration. Psychiatry Res 2001 Apr 10;106(2):141150.CrossRefGoogle ScholarPubMed
Raz, S.Raz, N.Structural brain abnormalities in the major psychoses: a quantitative review of the evidence from computerized imaging. Psychol Bull 1990 Jul;108(1):93108.CrossRefGoogle ScholarPubMed
Reveley, A.M.Reveley, M.A.Clifford, C.A.Murray, R.M.Cerebral ventricular size in twins discordant for schizophrenia. Lancet 1982 Mar 6;1(8271):540541.CrossRefGoogle Scholar
Rijsdijk, F.V.van Haren, N.E.Picchioni, M.M.McDonald, C.Toulopoulou, T.Pol, H.E.et al.Brain MRI abnormalities in schizophrenia: same genes or same environment?. Psychol Med 2005 Oct;35(10):13991409.CrossRefGoogle ScholarPubMed
Rossi, A.Bustini, M.Prosperini, P.Marinangeli, M.G.Splendiani, A.Daneluzzo, E.et al.Neuromorphological abnormalities in schizophrenic patients with good and poor outcome. Acta Psychiatr Scand 2000 Feb;101(2):161166.CrossRefGoogle ScholarPubMed
Rujescu, D.Meisenzahl, E.M.Giegling, I.Kirner, A.Leinsinger, G.Hegerl, U.et al.Methionine homozygosity at codon 129 in the prion protein is associated with white matter reduction and enlargement of CSF compartments in healthy volunteers and schizophrenic patients. Neuroimage 2002 Jan;15(1):200206.CrossRefGoogle ScholarPubMed
Scheepers, F.E.de Wied, C.C.Hulshoff Pol, H.E.van de, F.W.Van Der Linden, J.A.Kahn, R.S.The effect of clozapine on caudate nucleus volume in schizophrenic patients previously treated with typical antipsychotics. Neuropsychopharmacology 2001 Jan;24(1):4754.CrossRefGoogle ScholarPubMed
Schnack, H.G.van Haren, N.E.M.Hulshoff Pol, H.E.Picchioni, M.Weisbrod, M.Sauer, H.et al.Reliability of brain volumes from multicenter MRI acquisition: a calibration study. Hum Brain Mapp 2004;22:312320.CrossRefGoogle ScholarPubMed
Seidman, L.J.Faraone, S.V.Goldstein, J.M.Goodman, J.M.Kremen, W.S.Toomey, R.et al.Thalamic and amygdala-hippocampal volume reductions in first-degree relatives of patients with schizophrenia: an MRI-based morphometric analysis. Biol Psychiatry 1999 Oct 1;46(7):941954.CrossRefGoogle ScholarPubMed
Sharma, T.Lancaster, E.Lee, D.Lewis, S.Sigmundsson, T.Takei, N.et al.Brain changes in schizophrenia. Volumetric MRI study of families multiply affected with schizophrenia–the Maudsley family study 5. Br J Psychiatry 1998 Aug;173:132138.CrossRefGoogle ScholarPubMed
Silverman, J.M.Smith, C.J.Guo, S.L.Mohs, R.C.Siever, L.J.Davis, K.L.Lateral ventricular enlargement in schizophrenic probands and their siblings with schizophrenia-related disorders. Biol Psychiatry 1998 Jan 15;43(2):97106.CrossRefGoogle ScholarPubMed
Spinks, R.Nopoulos, P.Ward, J.Fuller, R.Magnotta, V.A.Andreasen, N.C.Globus pallidus volume is related to symptom severity in neuroleptic naive patients with schizophrenia. Schizophr Res 2005 Mar 1;73(2–3):229233.CrossRefGoogle ScholarPubMed
Sponheim, S.R.Iacono, W.G.Beiser, M.Stability of ventricular size after the onset of psychosis in schizophrenia. Psychiatry Res 1991 May;40(1):2129.CrossRefGoogle ScholarPubMed
Sporn, A.L.Greenstein, D.K.Gogtay, N.Jeffries, N.O.Lenane, M.Gochman, P.et al.Progressive brain volume loss during adolescence in childhood-onset schizophrenia. Am J Psychiatry 2003 Dec;160(12):21812189.CrossRefGoogle ScholarPubMed
Staal, W.G.Hulshoff Pol, H.E.Kahn, R.S.Outcome of schizophrenia in relation to brain abnormalities. Schizophr Bull 1999;25(2):337348.CrossRefGoogle ScholarPubMed
Staal, W.G.Hulshoff Pol, H.E.Schnack, H.van der Schot, A.C.Kahn, R.S.Partial volume decrease of the thalamus in relatives of patients with schizophrenia. Am J Psychiatry 1998 Dec;155(12):17841786.CrossRefGoogle ScholarPubMed
Staal, W.G.Hulshoff Pol, H.E.Schnack, H.G.Hoogendoorn, M.L.Jellema, K.Kahn, R.S.Structural brain abnormalities in patients with schizophrenia and their healthy siblings. Am J Psychiatry 2000 Mar;157(3):416421.CrossRefGoogle ScholarPubMed
Staal, W.G.Hulshoff Pol, H.E.Schnack, H.G.van Haren, N.E.Seifert, N.Kahn, R.S.Structural brain abnormalities in chronic schizophrenia at the extremes of the outcome spectrum. Am J Psychiatry 2001 Jul;158(7):11401142.CrossRefGoogle ScholarPubMed
Steen, R.G.Mull, C.McClure, R.Hamer, R.M.Lieberman, J.A.Brain volume in first-episode schizophrenia: systematic review and meta-analysis of magnetic resonance imaging studies. Br J Psychiatry 2006 Jun;188:510518.CrossRefGoogle ScholarPubMed
Suddath, R.L.Christison, G.W.Torrey, E.F.Casanova, M.F.Weinberger, D.R.Anatomical abnormalities in the brains of monozygotic twins discordant for schizophrenia. [published erratum appears in N Engl J Med 1990 May 31;322(22):1616; see comments]N Engl J Med 1990 Mar 22;322(12):789794.Google Scholar
Szeszko, P.R.Lipsky, R.Mentschel, C.Robinson, D.Gunduz-Bruce, H.Sevy, S.et al.Brain-derived neurotrophic factor Val66Met polymorphism and volume of the hippocampal formation. Mol Psychiatry 2005 Jul;10(7):631636.CrossRefGoogle ScholarPubMed
Upadhyaya, A.R.El-Sheikh, R.MacMaster, F.P.Diwadkar, V.A.Keshavan, M.S.Pituitary volume in neuroleptic-naive schizophrenia: a structural MRI study. Schizophr Res 2007 Feb;90(1–3):266273.CrossRefGoogle ScholarPubMed
Van Horn, J.D.McManus, I.C.Ventricular enlargement in schizophrenia. A meta-analysis of studies of the ventricle:brain ratio (VBR). Br J Psychiatry 1992 May;160:687697.CrossRefGoogle Scholar
Vita, A.Giobbio, G.M.Dieci, M.Garbarini, M.Morganti, C.Comazzi, M.et al.Stability of cerebral ventricular size from the appearance of the first psychotic symptoms to the later diagnosis of schizophrenia. Biol Psychiatry 1994 Jun 15;35(12):960962.CrossRefGoogle ScholarPubMed
Vita, A.Sacchetti, E.Valvassori, G.Cazzullo, C.L.Brain morphology in schizophrenia: a 2- to 5-year CT scan follow-up study. Acta Psychiatr Scand 1988 Nov;78(5):618621.CrossRefGoogle ScholarPubMed
Wassink, T.H.Andreasen, N.C.Nopoulos, P.Flaum, M.Cerebellar morphology as a predictor of symptom and psychosocial outcome in schizophrenia. Biol Psychiatry 1999 Jan 1;45(1):4148.CrossRefGoogle Scholar
Weinberger, D.R.Computed tomography (CT) findings in schizophrenia: speculation on the meaning of it all. J Psychiatr Res 1984;18(4):477490.CrossRefGoogle Scholar
Weinberger, D.R.DeLisi, L.E.Neophytides, A.N.Wyatt, R.J.Familial aspects of CT scan abnormalities in chronic schizophrenic patients. Psychiatry Res 1981 Feb;4(1):6571.CrossRefGoogle ScholarPubMed
Weinberger, D.R.McClure, R.K.Neurotoxicity, neuroplasticity, and magnetic resonance imaging morphometry: what is happening in the schizophrenic brain?. Arch Gen Psychiatry 2002 Jun;59(6):553558.CrossRefGoogle ScholarPubMed
Westmoreland Corson, P.Nopoulos, P.Andreasen, N.C.Heckel, D.Arndt, S.Caudate size in first-episode neuroleptic-naive schizophrenic patients measured using an artificial neural network. Biol Psychiatry 1999 Sep 1;46(5):712720.CrossRefGoogle Scholar
Westmoreland Corson, P.W.Nopoulos, P.Miller, D.D.Arndt, S.Andreasen, N.C.Change in basal ganglia volume over 2 years in patients with schizophrenia: typical versus atypical neuroleptics. Am J Psychiatry 1999 Aug;156(8):12001204.Google Scholar
Wood, S.J.Velakoulis, D.Smith, D.J.Bond, D.Stuart, G.W.McGorry, P.D.et al.A longitudinal study of hippocampal volume in first episode psychosis and chronic schizophrenia. Schizophr Res 2001 Oct 1;52(1–2):3746.CrossRefGoogle ScholarPubMed
Woods, B.T.Is schizophrenia a progressive neurodevelopmental disorder? Toward a unitary pathogenetic mechanism. Am J Psychiatry 1998 Dec;155(12):16611670.CrossRefGoogle Scholar
Woods, B.T.Yurgelun-Todd, D.Benes, F.M.Frankenburg, F.R.Pope, H.G. Jr.McSparren, J.Progressive ventricular enlargement in schizophrenia: comparison to bipolar affective disorder and correlation with clinical course. Biol Psychiatry 1990 Feb 1;27(3):341352.CrossRefGoogle ScholarPubMed
Wright, I.C.Rabe-Hesketh, S.Woodruff, P.W.David, A.S.Murray, R.M.Bullmore, E.T.Meta-analysis of regional brain volumes in schizophrenia. Am J Psychiatry 2000 Jan;157(1):1625.CrossRefGoogle Scholar
Zammit, S.Allebeck, P.Andreasson, S.Lundberg, I.Lewis, G.Self reported cannabis use as a risk factor for schizophrenia in Swedish conscripts of 1969: historical cohort study. BMJ 2002 Nov 23;325(7374):1199.CrossRefGoogle ScholarPubMed
Rais, M.Cahn, W.Van Haren, N.Schnack, H.Caspers, E.Hulshoff Pol, H.et al.Excessive brain volume loss over time in cannabis-using first-episode schizophrenia patients. Am J Psychiatry 2008 Apr;165(4):490496.CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.