Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-10T07:04:16.842Z Has data issue: false hasContentIssue false

Fiber tracking of white matter integrity connecting the mediodorsal nucleus of the thalamus and the prefrontal cortex in schizophrenia: A diffusion tensor imaging study

Published online by Cambridge University Press:  16 April 2020

Shinsuke Kito*
Affiliation:
Department of Neuropsychiatry, Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo181-8611, Japan
Jiuk Jung
Affiliation:
Department of Electrical Engineering, Graduate School of Engineering, Kyoto University, Kyoto, Japan
Tetsuo Kobayashi
Affiliation:
Department of Electrical Engineering, Graduate School of Engineering, Kyoto University, Kyoto, Japan
Yoshihiko Koga
Affiliation:
Department of Neuropsychiatry, Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo181-8611, Japan
*
*Corresponding author. Tel.: +81 422 47 5511x2885; fax: +81 422 45 4697. E-mail address: kito@kk.iij4u.or.jp (S. Kito).
Get access

Abstract

The goal of this study was to detect abnormalities in white matter integrity connecting the mediodorsal nucleus of the thalamus and the prefrontal cortex using fiber-tracking technique. Diffusion tensor imaging was acquired in 20 patients with schizophrenia and 20 normal comparison subjects. Fiber tracking was performed on the anterior thalamic peduncle, and the tractography was used to determine the cross-sectional area, mean fractional anisotropy, and standard deviation of fractional anisotropy for every step separately in the right and left hemispheres. Compared with normal subjects, patients showed a significant reduction in the cross-sectional area of the left anterior thalamic peduncle. There were no significant differences for the mean fractional anisotropy bilaterally between the two groups, but significant differences for the standard deviation of fractional anisotropy in both hemispheres. Reduction in the cross-sectional area of the left anterior thalamic peduncle suggests the presence of the failure of left-hemisphere lateralization. In schizophrenic patients a significant increase of the standard deviation of fractional anisotropy raise the possibility that the inhomogeneity of white matter integrity, which is densely or sparsely distributed by site. These findings might provide further evidence for disruption of white matter integrity between the thalamus and the prefrontal cortex in schizophrenia.

Type
Original article
Copyright
Copyright © Elsevier Masson SAS 2009

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

Ardekani, B.A., Nierenberg, J., Hoptman, M.J., Javitt, D.C., Lim, K.O.MRI study of white matter diffusion anisotropy in schizophrenia. Neuroreport 2003;14:20252029.CrossRefGoogle Scholar
Ashtari, M., Cottone, J., Ardekani, B.A., Cervellione, K., Szeszko, P.R., Wu, J.et al.Disruption of white matter integrity in the inferior longitudinal fasciculus in adolescents with schizophrenia as revealed by fiber tractography. Arch Gen Psychiatry 2007;64:12701280.CrossRefGoogle ScholarPubMed
Basser, P.J., Pierpaoli, C.Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI. J Magn Reson Ser B 1996;111:209219.Google ScholarPubMed
Basser, P.J., Pajevic, S., Pierpaoli, C., Duda, J., Aldroubi, A.In vivo fiber tractography using DT-MRI data. Magn Reson Med 2000;44:625632.3.0.CO;2-O>CrossRefGoogle ScholarPubMed
Buchsbaum, M.S., Tang, C.Y., Peled, S., Gudbjartsson, H., Lu, D., Hazlett, E.A.et al.MRI white matter diffusion anisotropy and PET metabolic rate in schizophrenia. Neuroreport 1998;9:425430.CrossRefGoogle Scholar
Buchsbaum, M.S., Friedman, J., Buchsbaum, B.R., Chu, K.W., Hazlett, E.A., Newmark, R.et al.Diffusion tensor imaging in schizophrenia. Biol Psychiatry 2006;60:11811187.CrossRefGoogle Scholar
Buchsbaum, M.S., Schoenknecht, P., Torosjan, Y., Newmark, R., Chu, K.W., Mitelman, S.et al.Diffusion tensor imaging of frontal lobe white matter tracts in schizophrenia. Ann Gen Psychiatry 2006;5:19CrossRefGoogle Scholar
Burns, J., Job, D., Bastin, M.E., Whalley, H., Macgillivray, T., Johnstone, E.C.et al.Structural disconnectivity in schizophrenia: a diffusion tensor magnetic resonance imaging study. Br J Psychiatry 2003;182:439443.CrossRefGoogle ScholarPubMed
Byne, W., Buchsbaum, M.S., Kemether, E., Hazlett, E.A., Shinwari, A., Mitropoulou, V.et al.Magnetic resonance imaging of the thalamic mediodorsal nucleus and pulvinar in schizophrenia and schizotypal personality disorder. Arch Gen Psychiatry 2001;58:133140.CrossRefGoogle ScholarPubMed
Byne, W., Buchsbaum, M.S., Mattiace, L.A., Hazlett, E.A., Kemether, E., Elhakem, S.L.et al.Postmortem assessment of thalamic nuclear volumes in subjects with schizophrenia. Am J Psychiatry 2002;159:5965.CrossRefGoogle ScholarPubMed
Conturo, T.E., Lori, N.F., Cull, T.S., Akbudak, E., Snyder, A.Z., Shimony, J.S.et al.Tracking neuronal fiber pathways in the living human brain. Proc Natl Acad Sci USA 1999;96:1042210427.Google ScholarPubMed
Hakak, Y., Walker, J.R., Li, C., Wong, W.H., Davis, K.L., Buxbaum, J.D.et al.Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia. Proc Natl Acad Sci USA 2001;98:47464751.Google ScholarPubMed
Hof, P.R., Haroutunian, V., Copland, C., Davis, K.L., Buxbaum, J.D.Molecular and cellular evidence for an oligodendrocyte abnormality in schizophrenia. Neurochem Res 2002;27:11931200.CrossRefGoogle Scholar
Jones, D.K., Catani, M., Pierpaoli, C., Reeves, S.J., Shergill, S.S., O'Sullivan, M.et al.A diffusion tensor magnetic resonance imaging study of frontal cortex connections in very-late-onset schizophrenia-like psychosis. Am J Geriatr Psychiatry 2005;13:10921099.CrossRefGoogle ScholarPubMed
Jones, D.K., Catani, M., Pierpaoli, C., Reeves, S.J., Shergill, S.S., O'Sullivan, M.et al.Age effects on diffusion tensor magnetic resonance imaging tractography measures of frontal cortex connections in schizophrenia. Hum Brain Mapp 2006;27:230238.CrossRefGoogle Scholar
Kemether, E.M., Buchsbaum, M.S., Byne, W., Hazlett, E.A., Haznedar, M., Brickman, A.M.et al.Magnetic resonance imaging of mediodorsal, pulvinar, and centromedian nuclei of the thalamus in patients with schizophrenia. Arch Gen Psychiatry 2003;60:983991.CrossRefGoogle ScholarPubMed
Kubicki, M., McCarley, R., Westin, C.F., Park, H.J., Maier, S., Kikinis, R.et al.A review of diffusion tensor imaging studies in schizophrenia. J Psychiatr Res 2007;41:1530.CrossRefGoogle Scholar
Kubicki, M., Westin, C.F., Maier, S.E., Frumin, M., Nestor, P.G., Salisbury, D.F.et al.Uncinate fasciculus findings in schizophrenia: a magnetic resonance diffusion tensor imaging study. Am J Psychiatry 2002;159:813820.CrossRefGoogle ScholarPubMed
Kubicki, M., Westin, C.F., Nestor, P.G., Wible, C.G., Frumin, M., Maier, S.E.et al.Cingulate fasciculus integrity disruption in schizophrenia: a magnetic resonance diffusion tensor imaging study. Biol Psychiatry 2003;54:11711180.CrossRefGoogle ScholarPubMed
Lim, K.O., Hedehus, M., Moseley, M., de Crespigny, A., Sullivan, E.V., Pfefferbaum, A.Compromised white matter tract integrity in schizophrenia inferred from diffusion tensor imaging. Arch Gen Psychiatry 1999;56:367374.CrossRefGoogle ScholarPubMed
Minami, T., Nobuhara, K., Okugawa, G., Takase, K., Yoshida, T., Sawada, S.et al.Diffusion tensor magnetic resonance imaging of disruption of regional white matter in schizophrenia. Neuropsychobiology 2003;47:141145.Google Scholar
Mori, S., Crain, B.J., Chacko, V.P., van Zijl, P.C.Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging. Ann Neurol 1999;45:265269.3.0.CO;2-3>CrossRefGoogle ScholarPubMed
Okugawa, G., Nobuhara, K., Minami, T., Tamagaki, C., Takase, K., Sugimoto, T.et al.Subtle disruption of the middle cerebellar peduncles in patients with schizophrenia. Neuropsychobiology 2004;50:119123.CrossRefGoogle ScholarPubMed
Park, H.J., Westin, C.F., Kubicki, M., Maier, S.E., Niznikiewicz, M., Baer, A.et al.White matter hemisphere asymmetries in healthy subjects and in schizophrenia: a diffusion tensor MRI study. Neuroimage 2004;23:213223.Google ScholarPubMed
Press, W.H., Flannery, B.P., Teukolsky, S.A., Vetterling, W.T.Numerical recipes in C. The art of scientific computing Press, W.H.2nd ed.Cambridge: Cambridge University Press; 1993.Google Scholar
Price, G., Cercignani, M., Parker, G.J., Altmann, D.R., Barnes, T.R., Barker, G.J.et al.Abnormal brain connectivity in first-episode psychosis: a diffusion MRI tractography study of the corpus callosum. Neuroimage 2007;35:458466.CrossRefGoogle ScholarPubMed
Price, G., Cercignani, M., Parker, G.J., Altmann, D.R., Barnes, T.R., Barker, G.J.et al.White matter tracts in first-episode psychosis: a DTI tractography study of the uncinate fasciculus. Neuroimage 2008;39:949955.CrossRefGoogle ScholarPubMed
Shenton, M.E., Dickey, C.C., Frumin, M., McCarley, R.W.A review of MRI findings in schizophrenia. Schizophr Res 2001;49:152.CrossRefGoogle Scholar
Szeszko, P.R., Ardekani, B.A., Ashtari, M., Kumra, S., Robinson, D.G., Sevy, S.et al.White matter abnormalities in first-episode schizophrenia or schizoaffective disorder: a diffusion tensor imaging study. Am J Psychiatry 2005;162:602605.Google ScholarPubMed
Taylor, W.D., Hsu, E., Krishnan, K.R., MacFall, J.R.Diffusion tensor imaging: background, potential, and utility in psychiatric research. Biol Psychiatry 2004;55:201207.CrossRefGoogle ScholarPubMed
Uranova, N.A., Vostrikov, V.M., Orlovskaya, D.D., Rachmanova, V.I.Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium. Schizophr Res 2004;67:269275.CrossRefGoogle ScholarPubMed
Woods, S.W.Chlorpromazine equivalent doses for the newer atypical antipsychotics. J Clin Psychiatry 2003;64:663667.Google ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.