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1 - Structural imaging of schizophrenia

from Section I - Schizophrenia

Published online by Cambridge University Press:  10 January 2011

Thomas J. Whitford
Affiliation:
Department of Psychiatry Brigham and Women's Hospital Harvard School of Medicine Boston, MA, USA and Department of Psychiatry Melbourne Neuropsychiatry Centre University of Melbourne Melbourne, Australia
Marek Kubicki
Affiliation:
Department of Psychiatry VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA
Martha E. Shenton
Affiliation:
VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA
Martha E. Shenton
Affiliation:
VA Boston Healthcare System and Brigham and Women's Hospital, Harvard Medical School
Bruce I. Turetsky
Affiliation:
University of Pennsylvania
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Summary

Introduction

Emil Kraepelin, one of the founding fathers of the diagnostic concept of schizophrenia, argued that the disorder was underpinned by abnormalities in brain structure. In his 1899 textbook, Kraepelin wrote: “in dementia praecox [schizophrenia], partial damage to, or destruction of, cells of the cerebral cortex must probably occur” (Kraepelin,1907). Since that time, an enormous amount of research has been undertaken with an eye to determining whether or not Kraepelin was correct. Until recently, the question of whether patients with schizophrenia (SZ) exhibit abnormalities in brain structure was more or less synonymous with the question of whether they exhibit abnormalities in gray matter (GM). The GM, so-called because of its grayish appearance in post-mortem tissue sections, is thought to consist primarily of neuron bodies, dendrites, axon terminals and other synaptic infrastructure and certain classes of neuroglia. Until recently, the vast majority of research aimed at investigating the neuroanatomical underpinnings of SZ has focused on GM. This is perhaps understandable, given that GM comprises both the brain's fundamental units of information processing (neurons) and the sites-of-action for most psychotropic medications (synapses). In recent years, however, a growing proportion of contemporary research has begun to focus on the “other half of the brain” (as wryly denoted by Fields, 2004), i.e. the white matter. The white matter (WM) is primarily constituted of myelinated axon sheaths, which form the infrastructure for signal transmission between spatially discrete populations of neurons.

Type
Chapter
Information
Understanding Neuropsychiatric Disorders
Insights from Neuroimaging
, pp. 1 - 29
Publisher: Cambridge University Press
Print publication year: 2010

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References

Agartz, I, Andersson, J L and Skare, S. 2001. Abnormal brain white matter in schizophrenia: a diffusion tensor imaging study. Neuroreport 12, 2251–4.Google Scholar
Andreasen, N C. 1999. A unitary model of schizophrenia: Bleuler's “fragmented phrene” as schizencephaly. Arch Gen Psychiatry 56, 781–7.Google Scholar
Ardekani, B A, Nierenberg, J, Hoptman, M J, Javitt, D C and Lim, K O. 2003. MRI study of white matter diffusion anisotropy in schizophrenia Neuroreport 14, 2025–9.Google Scholar
Ashtari, M, Cottone, J, Ardekani, B, et al. 2007. Disruption of white matter integrity in the inferior longitudinal fasciculus in adolescents with schizophrenia as revealed by fiber tractography. Arch Gen Psychiatry 64, 1270–80.Google Scholar
Bartzokis, G. 2002. Schizophrenia: breakdown in the well-regulated lifelong process of brain development and maturation. Neuropsychopharmacology 27, 672–83.Google Scholar
Baumann, N and Pham-Dinh, D. 2001. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol Rev 81, 871–927.Google Scholar
Beaulieu, C and Allen, P. 1994. Determinants of anisotropic water diffusion in nerves. Mag Res Med 31, 394–400.Google Scholar
Bleuler, E. 1911. Dementia Praecox or the Group of Schizophrenias. New York, NY: International Universities Press.
Borgwardt, S, Riecher-Rössler, A, Dazzan, P, et al. 2007. Regional gray matter volume abnormalities in the at risk mental state. Biol Psychiatry 61, 1148–56.Google Scholar
Bourgeois, J P and Rakic, P. 1993. Changes of synaptic density in the primary visual cortex of the macaque monkey from fetal to adult stage. J Neurosci 13, 2801–20.Google Scholar
Brambilla, P, Cerini, R, Gasparini, A, et al. 2005. Investigation of corpus callosum in schizophrenia with diffusion imaging. Schizophr Res 79, 201–10.Google Scholar
Buchsbaum, M, Tang, C, Peled, S, et al. 1998. MRI white matter diffusion anisotropy and PET metabolic rate in schizophrenia. Neuroreport 9, 425–30.Google Scholar
Buchsbaum, M S, Friedman, J, Buchsbaum, B R, et al. 2006. Diffusion tensor imaging in schizophrenia. Biol Psychiatry 60, 1181–7.Google Scholar
Burns, J, Job, D, Bastin, M E, et al. 2003. Structural disconnectivity in schizophrenia: a diffusion tensor magnetic resonance imaging study. Br J Psychiatry 182, 439–43.Google Scholar
Butler, P, Hoptman, M, Nierenberg, J, Foxe, J, Javitt, D and Lim, K. 2006. Visual white matter integrity in schizophrenia. Am J Psychiatry 163, 2011–3.Google Scholar
Cahn, W, Pol, H E, Lems, E B, et al. 2002. Brain volume changes in first-episode schizophrenia: a 1-year follow-up study. Arch Gen Psychiatry 59, 1002–10.Google Scholar
Cheung, V, Cheung, C, McAlonan, G, et al. 2008. A diffusion tensor imaging study of structural dysconnectivity in never-medicated, first-episode schizophrenia. Psychol Med 38, 877–85.Google Scholar
Crow, T. 1998. Schizophrenia as a transcallosal misconnection syndrome. Schizophr Res 30, 111–4.Google Scholar
Davatzikos, C. 2004. Why voxel-based morphometric analysis should be used with great caution when characterizing group differences. Neuroimage 23, 17–20.Google Scholar
Bellis, M, Keshavan, M, Beers, S, et al. 2001. Sex differences in brain maturation during childhood and adolescence. Cereb Cortex 11, 552–7.Google Scholar
Douaud, G, Smith, S, Jenkinson, M, et al. 2007. Anatomically related grey and white matter abnormalities in adolescent-onset schizophrenia. Brain 130, 2375–86.Google Scholar
Ellison-Wright, I, Glahn, D, Laird, A, Thelen, S and Bullmore, E. 2008. The anatomy of first-episode and chronic schizophrenia: an anatomical likelihood estimation meta-analysis. Am J Psychiatry 165, 1015–23.Google Scholar
Ennis, D and Kindlmann, G. 2006. Orthogonal tensor invariants and the analysis of diffusion tensor magnetic resonance images. Magn Reson Med 55, 136–46.Google Scholar
Federspiel, A, Begré, S, Kiefer, C, Schroth, G, Strik, W and Dierks, T. 2006. Alterations of white matter connectivity in first episode schizophrenia. Neurobiol Dis 22, 702–9.Google Scholar
Feinberg, I. 1978. Efference copy and corollary discharge: implications for thinking and its disorders. Schizophr Bull 4, 636–40.Google Scholar
Feinberg, I. 1982. Schizophrenia: caused by a fault in programmed synaptic elimination during adolescence? J Psychiatr Res 17, 319–34.Google Scholar
Fields, R. 2004. The other half of the brain. Sci Am 290, 54–61.Google Scholar
Fields, R. 2008. White matter in learning, cognition and psychiatric disorders. Trends Neurosci 31, 361–70.Google Scholar
Foong, J, Maier, M, Clark, C A, Barker, G J, Miller, D H and Ron, M A. 2000. Neuropathological abnormalities of the corpus callosum in schizophrenia: a diffusion tensor imaging study. J Neurol Neurosurg Psychiatry 68, 242–4.Google Scholar
Foong, J, Symms, M R, Barker, G J, Maier, M, Miller, D H and Ron, M A. 2002. Investigating regional white matter in schizophrenia using diffusion tensor imaging. Neuroreport 13, 333–6.Google Scholar
Ford, J M, Mathalon, D H, Heinks, T, Kalba, S, Faustman, W O and Roth, W T. 2001. Neurophysiological evidence of corollary discharge dysfunction in schizophrenia. Am J Psychiatry 158, 2069–71.Google Scholar
Friedman, J, Tang, C, Carpenter, D, et al. 2008. Diffusion tensor imaging findings in first-episode and chronic schizophrenia patients. Am J Psychiatry 165, 1024–32.Google Scholar
Friston, K. 1999. Schizophrenia and the disconnection hypothesis. Acta Psychiatr Scand Suppl 395, 68–79.Google Scholar
Frith, C D. 1992. The Cognitive Neuropsychology of Schizophrenia. Hove, UK: Lawrence Erlbaum Associates.
Frith, C D, Blakemore, S and Wolpert, D M. 2000. Explaining the symptoms of schizophrenia: abnormalities in the awareness of action. Brain Res Rev 31, 357–63.Google Scholar
Frith, C D and Done, D J. 1989. Experiences of alien control in schizophrenia reflect a disorder in the central monitoring of action. Psychol Med 19, 359–63.Google Scholar
Fujiwara, H, Namiki, C, Hirao, K, et al. 2007. Anterior and posterior cingulum abnormalities and their association with psychopathology in schizophrenia: a diffusion tensor imaging study. Schizophr Res 95, 215–22.Google Scholar
Garner, B, Pariante, C, Wood, S, et al. 2005. Pituitary volume predicts future transition to psychosis in individuals at ultra-high risk of developing psychosis. Biol Psychiatry 58, 417–23.Google Scholar
Glahn, D, Laird, A, Ellison-Wright, I, et al. 2008. Meta-analysis of gray matter anomalies in schizophrenia: application of anatomic likelihood estimation and network analysis. Biol Psychiatry 64, 774–81.Google Scholar
Gur, R E, Cowell, P, Turetsky, B I, et al. 1998. A follow-up magnetic resonance imaging study of schizophrenia: relationship of neuroanatomical changes to clinical and neurobehavioral measures. Arch Gen Psychiatry 55, 145–52.Google Scholar
Gurrera, R, Nakamura, M, Kubicki, M, et al. 2007. The uncinate fasciculus and extraversion in schizotypal personality disorder: a diffusion tensor imaging study. Schizophr Res 90, 360–2.Google Scholar
Hao, Y, Liu, Z, Jiang, T, et al. 2006. White matter integrity of the whole brain is disrupted in first-episode schizophrenia. Neuroreport 17, 23–6.Google Scholar
Hirayasu, Y, Tanaka, S, Shenton, M E, et al. 2001. Prefrontal gray matter volume reduction in first episode schizophrenia. Cerebral Cortex 11, 374–81.Google Scholar
Honea, R, Crow, T J, Passingham, D and Mackay, C E. 2005. Regional deficits in brain volume in schizophrenia: a meta-analysis of voxel-based morphometry studies. Am J Psychiatry 162, 2233–45.Google Scholar
Hubl, D, Koenig, T, Strik, W, et al. 2004. Pathways that make voices: white matter changes in auditory hallucinations. Arch Gen Psychiatry 61, 658–68.Google Scholar
Jahanshahi, M and Frith, C. 1998. Willed action and its impairments. Cogn Neuropsychol 15, 483.Google Scholar
Jones, D K, Catani, M, Pierpaoli, C, et al. 2006. Age effects on diffusion tensor magnetic resonance imaging tractography measures of frontal cortex connections in schizophrenia. Hum Brain Mapp 27, 230–8.Google Scholar
Kanaan, R A, Kim, J S, Kaufmann, W E, Pearlson, G D, Barker, G J and McGuire, P K. 2005. Diffusion tensor imaging in schizophrenia. Biol Psychiatry 58, 921–9.Google Scholar
Kanaan, R A, Shergill, S S, Barker, G J, et al. 2006. Tract-specific anisotropy measurements in diffusion tensor imaging. Psychiatry Res 146, 73–82.Google Scholar
Karlsgodt, K, Erp, T, Poldrack, R, Bearden, C, Nuechterlein, K and Cannon, T. 2008. Diffusion tensor imaging of the superior longitudinal fasciculus and working memory in recent-onset schizophrenia. Biol Psychiatry 63, 512–8.Google Scholar
Kasai, K, Shenton, M E, Salisbury, D F, et al. 2003. 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 60, 766–75.Google Scholar
Kawashima, T, Nakamura, M, Boiux, S, et al. 2009. Uncinate fasciculus abnormalities in recent onset schizophrenia and affective psychosis: a diffusion tensor imaging study. Schiz Res 110, 119–26.Google Scholar
Kendi, M, Kendi, A, Lehericy, S, et al. 2008. Structural and diffusion tensor imaging of the fornix in childhood- and adolescent-onset schizophrenia. J Am Acad Child Adolesc Psychiatry 47, 826–32.Google Scholar
Keshavan, M S, Anderson, S and Pettegrew, J W. 1994. Is schizophrenia due to excessive synaptic pruning in the prefrontal cortex? The Feinberg hypothesis revisited. J Psychiatr Res 28, 239–65.Google Scholar
Konopaske, G, Dorph-Petersen, K, Sweet, R, et al. 2008. Effect of chronic antipsychotic exposure on astrocyte and oligodendrocyte numbers in macaque monkeys. Biol Psychiatry 63, 759–65.Google Scholar
Kraepelin, E, ed. 1907. Textbook of Psychiatry. London: Macmillan.
Kubicki, M, McCarley, R, Westin, C F, et al. 2007. A review of diffusion tensor imaging studies in schizophrenia. J Psychiatr Res 41, 15–30.Google Scholar
Kubicki, M, Park, H, Westin, C F, et al. 2005. DTI and MTR abnormalities in schizophrenia: analysis of white matter integrity. Neuroimage 26, 1109–18.Google Scholar
Kubicki, M, Westin, C F, Maier, S E, et al. 2002. Uncinate fasciculus findings in schizophrenia: a magnetic resonance diffusion tensor imaging study. Am J Psychiatry 159, 813–20.Google Scholar
Kubicki, M, Westin, C F, Nestor, P G, et al. 2003. Cingulate fasciculus integrity disruption in schizophrenia: a magnetic resonance diffusion tensor imaging study. Biol Psychiatry 54, 1171–80.Google Scholar
Kumra, S, Ashtari, M, Cervellione, K, et al. 2005. White matter abnormalities in early-onset schizophrenia: a voxel-based diffusion tensor imaging study. J Am Acad Child Adolesc Psychiatry 44, 934–41.Google Scholar
Kumra, S, Ashtari, M, McMeniman, M, et al. 2004. Reduced frontal white matter integrity in early-onset schizophrenia: a preliminary study. Biol Psychiatry 55, 1138–45.Google Scholar
Kuroki, N, Kubicki, M, Nestor, P G, et al. 2006. Fornix integrity and hippocampal volume in male schizophrenic patients. Biol Psychiatry 60, 22–31.Google Scholar
Kyriakopoulos, M, Vyas, N, Barker, G, Chitnis, X and Frangou, S. 2008. A diffusion tensor imaging study of white matter in early-onset schizophrenia. Biol Psychiatry 63, 519–23.Google Scholar
Lawrie, S M, Buechel, C, Whalley, H C, Frith, C D, Friston, K J and Johnstone, E C. 2002. Reduced frontotemporal functional connectivity in schizophrenia associated with auditory hallucinations. Biological Psychiatry 51, 1008–11.Google Scholar
Lim, K O, Hedehus, M, Moseley, M, Crespigny, A, Sullivan, E V and Pfefferbaum, A. 1999. Compromised white matter tract integrity in schizophrenia inferred from diffusion tensor imaging. Arch Gen Psychiatry 56, 367–74.Google Scholar
Manoach, D, Ketwaroo, G, Polli, F, et al. 2007. Reduced microstructural integrity of the white matter underlying anterior cingulate cortex is associated with increased saccadic latency in schizophrenia. Neuroimage 37, 599–610.Google Scholar
McIntosh, A M, Maniega, S M, Lymer, G K S, et al. 2008. White matter tractography in bipolar disorder and schizophrenia. Biol Psychiatry 64, 1088–92.Google Scholar
Minami, T, Nobuhara, K, Okugawa, G, et al. 2003. Diffusion tensor magnetic resonance imaging of disruption of regional white matter in schizophrenia. Neuropsychobiology 47, 141–5.Google Scholar
Mitelman, S, Torosjan, Y, Newmark, R, et al. 2007. Internal capsule, corpus callosum and long associative fibers in good and poor outcome schizophrenia: a diffusion tensor imaging survey. Schizophr Res 92, 211–24.Google Scholar
Miyata, J, Hirao, K, Namiki, C, et al. 2007. Interfrontal commissural abnormality in schizophrenia: tractography-assisted callosal parcellation. Schizophr Res 97, 236–41.Google Scholar
Mori, T, Ohnishi, T, Hashimoto, R, et al. 2007. Progressive changes of white matter integrity in schizophrenia revealed by diffusion tensor imaging. Psychiatry Res 154, 133–45.Google Scholar
Nestor, P, Kubicki, M, Niznikiewicz, M, Gurrera, R, McCarley, R and Shenton, M. 2008. Neuropsychological disturbance in schizophrenia: a diffusion tensor imaging study. Neuropsychology 22, 246–54.Google Scholar
O'Daly, O, Frangou, S, Chitnis, X and Shergill, S. 2007. Brain structural changes in schizophrenia patients with persistent hallucinations. Psychiatry Res 156, 15–21.Google Scholar
Pakkenberg, B. 1993. Total nerve cell number in neocortex in chronic schizophrenics and controls estimated using optical dissectors. Biol Psychiatry 34, 768–72.Google Scholar
Pantelis, C, Velakoulis, D, McGorry, P D, et al. 2003. Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison. Lancet 361, 281–8.Google Scholar
Park, H J, Westin, C F, Kubicki, M, et al. 2004. White matter hemisphere asymmetries in healthy subjects and in schizophrenia: a diffusion tensor MRI study. Neuroimage 23, 213–23.Google Scholar
Pearlson, G D and Marsh, L. 1999. Structural brain imaging in schizophrenia: a selective review. Biol Psychiatry 46, 627–49.Google Scholar
Pekny, M and Nilsson, M. 2005. Astrocyte activation and reactive gliosis. Glia 50, 427–34.Google Scholar
Pfefferbaum, A, Mathalon, D H, Sullivan, E V, Rawles, J M, Zipursky, R B and Lim, K O. 1994. A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood. Arch Neurol 51, 874–87.Google Scholar
Pfefferbaum, A and Sullivan, E V. 2003. Increased brain white matter diffusivity in normal adult aging: relationship to anisotropy and partial voluming. Magn Reson Med 49, 953–61.Google Scholar
Price, G, Bagary, M S, Cercignani, M, Altmann, D R and Ron, M A. 2005. The corpus callosum in first episode schizophrenia: a diffusion tensor imaging study. J Neurol Neurosurg Psychiatry 76, 585–7.Google Scholar
Price, G, Cercignani, M, Bagary, M, et al. 2006. A volumetric MRI and magnetization transfer imaging follow-up study of patients with first-episode schizophrenia. Schizophr Res 87, 100–08.Google Scholar
Price, G, Cercignani, M, Parker, G, et al. 2008. White matter tracts in first-episode psychosis: a DTI tractography study of the uncinate fasciculus. Neuroimage 39, 949–55.Google Scholar
Price, G, Cercignani, M, Parker, G J, et al. 2007. Abnormal brain connectivity in first-episode psychosis: a diffusion MRI tractography study of the corpus callosum. Neuroimage 35, 458–66.Google Scholar
Purves, D and Lichtman, J W. 1980. Elimination of synapses in the developing nervous system. Science 210, 153–7.Google Scholar
Roberts, G, Colter, N, Lofthouse, R, Bogerts, B, Zech, M and Crow, T. 1986. Gliosis in schizophrenia: a survey. Biol Psychiatry 21, 1043–50.Google Scholar
Rosenberger, G, Kubicki, M, Nestor, P, et al. 2008. Age-related deficits in fronto-temporal connections in schizophrenia: a diffusion tensor imaging study. Schizophr Res 102, 181–8.Google Scholar
Rotarska-Jagiela, A and Linden, D. 2008. The corpus callosum in schizophrenia-volume and connectivity changes affect specific regions. Neuroimage 39, 1522–32.Google Scholar
Roy, K, Murtie, J, El-Khodor, B, et al. 2007. Loss of erbB signaling in oligodendrocytes alters myelin and dopaminergic function, a potential mechanism for neuropsychiatric disorders. Proc Natl Acad Sci U S A 104, 8131–6.Google Scholar
Salisbury, D, Kuroki, N, Kasai, K, Shenton, M and McCarley, R. 2007. Progressive and interrelated functional and structural evidence of post-onset brain reduction in schizophrenia. Arch Gen Psychiatry 64, 521–9.Google Scholar
Scherk, H and Falkai, P. 2006. Effects of antipsychotics on brain structure. Curr Opin Psychiatry 19, 145–50.Google Scholar
Schlösser, R, Nenadic, I, Wagner, G, et al. 2007. White matter abnormalities and brain activation in schizophrenia: a combined DTI and fMRI study. Schizophr Res 89, 1–11.Google Scholar
Schneiderman, J S, Buchsbaum, M S, Haznedar, M, et al. 2009. Age and diffusion anisotropy in adolescent and adult patients with schizophrenia. Neuroimage 45, 662–71.Google Scholar
Seal, M, Yücel, M, Fornito, A, et al. 2008. Abnormal white matter microstructure in schizophrenia: a voxelwise analysis of axial and radial diffusivity. Schizophr Res 101, 106–10.Google Scholar
Seeman, P and Kapur, S. 2000. Schizophrenia: more dopamine, more D2 receptors. Proc Natl Acad Sci U S A 97, 7673–5.Google Scholar
Selemon, L D and Goldman-Rakic, P S. 1999. The reduced neuropil hypothesis: a circuit based model of schizophrenia. Biol Psychiatry 45, 17–25.Google Scholar
Seok, J, Park, H, Chun, J, et al. 2007. White matter abnormalities associated with auditory hallucinations in schizophrenia: a combined study of voxel-based analyses of diffusion tensor imaging and structural magnetic resonance imaging. Psychiatry Res 156, 93–104.Google Scholar
Shenton, M, Dickey, C, Frumin, M and McCarley, R. 2001. A review of MRI findings in schizophrenia. Schizophr Res 49, 1–52.Google Scholar
Shergill, S, Kanaan, R, Chitnis, X, et al. 2007. A diffusion tensor imaging study of fasciculi in schizophrenia. Am J Psychiatry 164, 467–73.Google Scholar
Song, S, Sun, S, Ju, W, Lin, S, Cross, A and Neufeld, A. 2003. Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia. Neuroimage 20, 1714–22.Google Scholar
Song, S, Sun, S, Ramsbottom, M, Chang, C, Russell, J and Cross, A. 2002. Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water. Neuroimage 17, 1429–36.Google Scholar
Stangel, M. 2004. Remyelinating and neuroprotective treatments in multiple sclerosis. Expert Opin Investig Drugs 13, 331–47.Google Scholar
Steen, R, Mull, C, McClure, R, Hamer, R and Lieberman, J. 2006. Brain volume in first-episode schizophrenia: systematic review and meta-analysis of magnetic resonance imaging studies. Br J Psychiatry 188, 510–8.Google Scholar
Steen, R G, Ogg, R J, Reddick, W E and Kingsley, P B. 1997. Age-related changes in the pediatric brain: quantitative MR evidence of maturational changes during adolescence. Am J Neuroradiol 18, 819–28.Google Scholar
Sun, D, Stuart, G, Jenkinson, M, et al. 2009. Brain surface contraction mapped in first-episode schizophrenia: a longitudinal magnetic resonance imaging study. Mol Psychiatry 14, 976–86.Google Scholar
Sun, Z, Wang, F, Cui, L, et al. 2003. Abnormal anterior cingulum in patients with schizophrenia: a diffusion tensor imaging study. Neuroreport 14, 1833–6.Google Scholar
Szeszko, P, Robinson, D, Ashtari, M, et al. 2008. Clinical and neuropsychological correlates of white matter abnormalities in recent onset schizophrenia. Neuropsychopharmacology 33, 976–84.Google Scholar
Takei, K, Yamasue, H, Abe, O, et al. 2008. Disrupted integrity of the fornix is associated with impaired memory organization in schizophrenia. Schizophr Res 103, 52–61.Google Scholar
Thompson, C. 1995. Apoptosis in the pathogenesis and treatment of disease. Science 267, 1456–62.Google Scholar
Uranova, N, Vostrikov, V, Vikhreva, O, Zimina, I, Kolomeets, N and Orlovskaya, D. 2007. The role of oligodendrocyte pathology in schizophrenia. Int J Neuropsychopharmacol 10, 537–45.Google Scholar
Haren, N, Hulshoff Pol, H, Schnack, H, et al. 2008. Progressive brain volume loss in schizophrenia over the course of the illness: evidence of maturational abnormalities in early adulthood. Biol Psychiatry 63, 106–13.Google Scholar
Vita, A, Peri, L, Silenzi, C and Dieci, M. 2006. Brain morphology in first-episode schizophrenia: a meta-analysis of quantitative magnetic resonance imaging studies. Schizophr Res 82, 75–88.Google Scholar
Walterfang, M, Wood, S, Velakoulis, D, Copolov, D and Pantelis, C. 2005. Diseases of white matter and schizophrenia-like psychosis. Aust N Z J Psychiatry 39, 746–56.Google Scholar
Wang, F, Sun, Z, Cui, L, et al. 2004. Anterior cingulum abnormalities in male patients with schizophrenia determined through diffusion tensor imaging. Am J Psychiatry 161, 573–5.Google Scholar
White, T, Kendi, A, Lehéricy, S, et al. 2007. Disruption of hippocampal connectivity in children and adolescents with schizophrenia – a voxel-based diffusion tensor imaging study. Schizophr Res 90, 302–7.Google Scholar
Whitford, T J, Grieve, S M, Farrow, T F, et al. 2006. Progressive grey matter atrophy over the first 2–3 years of illness in first-episode schizophrenia: a tensor-based morphometry study. NeuroImage 32, 511–9.Google Scholar
Whitford, T J, Grieve, S M, Farrow, T F, et al. 2007a. Volumetric white matter abnormalities in first-episode schizophrenia: a longitudinal, tensor-based morphometry study. Am J Psychiatry 164, 1082–9.Google Scholar
Whitford, T J, Kubicki, M and Shenton, M E, in press. Diffusion tensor imaging (DTI), schizophrenia and discrete brain regions. US Psychiatric Rev.
Whitford, T J, Rennie, C J, Grieve, S M, Clark, C R, Gordon, E and Williams, L M. 2007b. Brain maturation in adolescence: concurrent changes in neuroanatomy and neurophysiology. Human Brain Mapp 28, 228–37.Google Scholar
Wolkin, A, Choi, S, Szilagyi, S, Sanfilipo, M, Rotrosen, J and Lim, K. 2003. Inferior frontal white matter anisotropy and negative symptoms of schizophrenia: a diffusion tensor imaging study. Am J Psychiatry 160, 572–4.Google Scholar
Wood, S, Pantelis, C, Velakoulis, D, Yücel, M, Fornito, A and McGorry, P. 2008. Progressive changes in the development toward schizophrenia: studies in subjects at increased symptomatic risk. Schizophr Bull 34, 322–9.Google Scholar
Yakovlev, P, Lecours, A and Minkowski, A. 1967. Regional development of the brain early in life. Boston, MA: Blackwell Scientific Publications, pp. 3–70.
Yücel, M, Wood, S, Phillips, L, et al. 2003. Morphology of the anterior cingulate cortex in young men at ultra-high risk of developing a psychotic illness. Br J Psychiatry 182, 518–24.Google Scholar
Zahajszky, J, Dickey, C, McCarley, R, et al. 2001. A quantitative MR measure of the fornix in schizophrenia. Schizophr Res 47, 87–97.Google Scholar
Zhou, Y, Shu, N, Liu, Y, et al. 2008. Altered resting-state functional connectivity and anatomical connectivity of hippocampus in schizophrenia. Schizophr Res 100, 120–32.Google Scholar
Zou, L, Xie, J, Yuan, H, Pei, X, Dong, W and Liu, P. 2008. Diffusion tensor imaging study of the anterior limb of internal capsules in neuroleptic-naive schizophrenia. Acad Radiol 15, 285–9.Google Scholar

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  • Structural imaging of schizophrenia
    • By Thomas J. Whitford, Department of Psychiatry Brigham and Women's Hospital Harvard School of Medicine Boston, MA, USA and Department of Psychiatry Melbourne Neuropsychiatry Centre University of Melbourne Melbourne, Australia, Marek Kubicki, Department of Psychiatry VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA, Martha E. Shenton, VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA
  • Edited by Martha E. Shenton, Bruce I. Turetsky, University of Pennsylvania
  • Book: Understanding Neuropsychiatric Disorders
  • Online publication: 10 January 2011
  • Chapter DOI: https://doi.org/10.1017/CBO9780511782091.002
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  • Structural imaging of schizophrenia
    • By Thomas J. Whitford, Department of Psychiatry Brigham and Women's Hospital Harvard School of Medicine Boston, MA, USA and Department of Psychiatry Melbourne Neuropsychiatry Centre University of Melbourne Melbourne, Australia, Marek Kubicki, Department of Psychiatry VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA, Martha E. Shenton, VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA
  • Edited by Martha E. Shenton, Bruce I. Turetsky, University of Pennsylvania
  • Book: Understanding Neuropsychiatric Disorders
  • Online publication: 10 January 2011
  • Chapter DOI: https://doi.org/10.1017/CBO9780511782091.002
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  • Structural imaging of schizophrenia
    • By Thomas J. Whitford, Department of Psychiatry Brigham and Women's Hospital Harvard School of Medicine Boston, MA, USA and Department of Psychiatry Melbourne Neuropsychiatry Centre University of Melbourne Melbourne, Australia, Marek Kubicki, Department of Psychiatry VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA, Martha E. Shenton, VA Boston Healthcare System and Department of Psychiatry Brigham and Women's Hospital Harvard Medical School Boston, MA, USA
  • Edited by Martha E. Shenton, Bruce I. Turetsky, University of Pennsylvania
  • Book: Understanding Neuropsychiatric Disorders
  • Online publication: 10 January 2011
  • Chapter DOI: https://doi.org/10.1017/CBO9780511782091.002
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