Corpus Callosum Volume in Patients with First-Episode Psychosis
Year 2022,
Volume: 12 Issue: 2, 331 - 336, 30.06.2022
Onur Ağdanlı
Ahmet Topuzoglu
,
Nuri Karabay
,
Köksal Alptekin
Abstract
Objective In first-episode psychosis, a relationship may exist between disruption communication between two brain hemispheres and psychosis symptomatology. We aimed to investigate the relationship between corpus callosum (CC) volume and psychosis symptomatology in patients with first-episode psychosis.
Methods This is a retrospective case-control study wherein first-episode psychosis cases and healthy controls were included from inpatient unit archives of the Department of Psychiatry and Department of Radiology, Dokuz Eylül University School of Medicine. Psychosis symptoms were assessed using the positive and negative syndrome scale (PANSS). The CC, the chief connection between two brain hemispheres, was examined using magnetic resonance imaging (MRI); 27 patients with first-episode psychosis and 29 healthy volunteers were evaluated via 1.5-T MR. MRI findings of CC volumes of the two groups were compared. Correlations between PANSS scores and CC volume were also evaluated.
Results The CC volume was lower in patients with first-episode psychosis than in healthy controls. Moreover, we observed a significant negative correlation between the CC volume and emotional withdrawal scores, and a significant positive correlation between the CC volume and hallucinations.
Conclusions The CC is a vital structure that connects two frontal lobes of the brain. There may be CC abnormalities in first-episode psychosis. Emotional withdrawal is associated with decreased CC volume, whereas hallucinations are associated with increased CC volume. The development of these symptoms may be associated with changes in CC connections.
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high-risk cohorts: a review highlighting potential vulnerability
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cerebral white matter may underlie psychosis exacerbation.
Psychiatry Res. 2004; 130: 71-78.
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Toshikiko K. Olanzapine increases grey and white matter
volumes in the caudate nucleus of patients with schizophrenia.
Neuropsychobiology 2007; 55: 43-46.
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N. Differential effects of typical and atypical antipsychotics on
brain myelination in schizophrenia. Schizophr. Res. 2007; 93:
13-22.
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Bedwell JS. Abnormal neurologic maturation in adolescents
with early-onset schizophrenia. Am. J. Psychiatry 2001; 158:
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developmental deviance and premorbid dysfunction in early
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46: 1145-1150.
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A, David AS. Corpus callosum area and functioning in
schizophrenic patients with auditory-verbal hallucinations.
Schizophr Res. 2001; 50: 9-17.
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corpus callosum size in first-episode schizophrenics. Biol.
Psychiatry 1994; 35: 913-919.
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Green WD, Sweeney JA, et al. Landmark-based morphometric
analysis of first-episode schizophrenia. Biol. Psychiatry 1999;
45: 1321-1328.
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in schizophrenia: a diffusion tensor imaging study. J Neurol
Neurosurg Psychiatry 2000; 68: 242–244.
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Holzinger S. Structural correlates of psychopathological
symptom dimensions in schizophrenia: A voxel-based
morphometric study. NeuroImage 2008; 39: 1600–1612.
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schizophrenia: a cross-sectional study in first-episode and
chronic illness. Br J Psychiatry. 2008; 192: 429–434.
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in schizophrenia and schizotypal personality disorder.
Schizophr. Res. 2000; 42: 193–208.
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R, Alvarado JL, et al. Corpus Callosum Abnormalities and
their Association with Psychotic Symptoms in Patients with
Schizophrenia. Biol. Psychiatry. 2010; 68:70–77
Year 2022,
Volume: 12 Issue: 2, 331 - 336, 30.06.2022
Onur Ağdanlı
Ahmet Topuzoglu
,
Nuri Karabay
,
Köksal Alptekin
References
- [1] Andreasen NC. Neuroimaging. Teaching and learning about
schizophrenia. Module 2, 10-19.WPA, 1994.
- [2] Pearlson G. D., Marsh L., Magnetic resonance imaging in
psychiatry. Review of Psychiatry 1993; 12 (13): 347-381.
- [3] Bachmann S, Pantel J, Flender A, Bottmer C. Corpus callosum
in first-episode patients with schizophrenia a magnetic
resonance imaging study. Psychol. Med. 2003; 33:1019-1027.
- [4] Keshavan MS, Diwadkar VA, Harenski K, Rosenberg DR,
Sweeney JA, Pettegrew JW. Abnormalities of the corpus
callosum in first episode, treatment naive schizophrenia. J
Neurol Neurosurg Psychiatry 2002; 72:757-760.
- [5] Ross C. A, Pearlson G. D., Schizophrenia, The heteromodal
association neocortex and development: potential for a
neurogenetic approach. Trends in Neurosci. 1996; 19:171-176.
- [6] Hofer S, Frahm J. Topography of the human corpus callosum
revisited: comprehensive lif tractrography using diffusion
tensor magnetic resonance imaging. NeuroImage 2006; 32:
989-994.
- [7] Taylor WD, Hsu E, Krishnan KR, MacFall JR. Diffusion tensor
imaging: background, potential and utility in psychiatric
research. Biol Psychiatry 2004; 55:201-207.
- [8] Camchong J, Lim KO, Sponheim SR, MacDonald III AW. Frontal
white matter integrity as an endophenotype for schizophrenia:
diffusion tensor imaging in monozygotic twins and patients’
nonpsychotic relatives. Front. Hum. Neurosci. Vol;3 Article 35,
1-6.
- [9] Francis AN, Mothi SS, Mathew IT, Tandon N, Clementz B,
Pearlson GD. Callosal abnormalities across the psychosis
dimension: bipolar schizophrenia network on intermediate
phenotypes. Biol. Psychiatry 2016;80 (8), 627–635.
- [10] Mäkinen J, Miettunen J, Isohanni M, Koponen H. Negative
symptoms in schizophrenia—A review. Nord. J. Psychiatry
2008;62;5:334-340.
- [11] Arnone D, McIntosh AM, Tan GM, Ebmeier KP. Meta-analysis
of magnetic resonance imaging studies of the corpus callosum
in schizophrenia. Schizophr. Res. 2008; 101: 124-132.
- [12] Brewer W, Wood S, Phillips L, Francey MS, Pantelis C, Yung
AR. Generalized and specific cognitive performance in clinical
high-risk cohorts: a review highlighting potential vulnerability
markers for psychosis. Schizophr Bull. 2006; 32:538-555.
- [13] Christensen J, Holcomb J, Garver DL. State-related changes in
cerebral white matter may underlie psychosis exacerbation.
Psychiatry Res. 2004; 130: 71-78.
- [14] Okugawa G, Nobuhara K, Takase K, Saito Y, Yoshimura M,
Toshikiko K. Olanzapine increases grey and white matter
volumes in the caudate nucleus of patients with schizophrenia.
Neuropsychobiology 2007; 55: 43-46.
- [15] Bartzokis G, Lu PH, Nuechterlein KH, Gitlin M, Doi J, Edwards
N. Differential effects of typical and atypical antipsychotics on
brain myelination in schizophrenia. Schizophr. Res. 2007; 93:
13-22.
- [16] Karp BI, Garvey M, Jacobsen LK, Frazier JA, Hamburger SD,
Bedwell JS. Abnormal neurologic maturation in adolescents
with early-onset schizophrenia. Am. J. Psychiatry 2001; 158:
118-122.
- [17] Vourdas A, Pipe R, Corrigall R, Frangou S. Increased
developmental deviance and premorbid dysfunction in early
onset schizophrenia. Schizophr. Res. 2003; 62: 13-22.
- [18] Pujol J, Vendrell P, Junque C, Martí-Vilalta JL, Capdevila A.
When does human brain development end? Evidence of
corpus callosum growth up to adulthood. Ann. Neurol. 1993;
34: 71-75.
- [19] McCarley RW, Wible CG, Frumin M, Hirayasu Y, Levitt JJ, Fischer
IA. MRI anatomy of schizophrenia. Biol. Psychiatry 1999; 45:
1099-1119.
- [20] Woodruff P, McManus I, David A. Meta-analysis of corpus
callosum size in schizophrenia. J Neurol Neurosurg Psychiatry
1995; 58: 457-461.
- [21] Li T, Wang Q, Zhang J, Rolls ET, Yang W, Palaniyappan L.
Brain-wide analysis of functional connectivity in first episode and chronic stages of schizophrenia. Schizophr
Bull. 2017;43(2):436-448.
- [22] Crow, TJ. Schizophrenia is a transcallosal misconnection
syndrome. Schizophr. Res. 1998; 30: 111-114.
- [23] Crow TJ, Ball J, Bloom SR, Brown R, Bruton CJ, Colter N.
Schizophrenia as an anomaly of development of cerebral
asymmetry. A postmortem study and a proposa concerning
the genetic basis of the disease. Arch. Gen. Psychiatry 1989;
46: 1145-1150.
- [24] Rossell SL, Shapleske J, Fukuda R, Woodruff PW, Simmons
A, David AS. Corpus callosum area and functioning in
schizophrenic patients with auditory-verbal hallucinations.
Schizophr Res. 2001; 50: 9-17.
- [25] Hoff AL, Neal C, Kushner M, DeLisi LE. Gender differences in
corpus callosum size in first-episode schizophrenics. Biol.
Psychiatry 1994; 35: 913-919.
- [26] DeQuardo JR, Keshavan MS, Bookstein FL, Bagwell WW,
Green WD, Sweeney JA, et al. Landmark-based morphometric
analysis of first-episode schizophrenia. Biol. Psychiatry 1999;
45: 1321-1328.
- [27] Foong, J., Maier, M., Clark, C. A., Barker GJ, Miller DH, Ron
MA. Neuropathological abnormalities of the corpus callosum
in schizophrenia: a diffusion tensor imaging study. J Neurol
Neurosurg Psychiatry 2000; 68: 242–244.
- [28] Koutsouleris N, Gaser C, Jäger M, Bottlender R, Frodl T,
Holzinger S. Structural correlates of psychopathological
symptom dimensions in schizophrenia: A voxel-based
morphometric study. NeuroImage 2008; 39: 1600–1612.
- [29] Walterfang M, Wood A, Reutens D, Wood SJ, Chen J, Velakoulis
D. Morphology of the corpus callosum at different stages of
schizophrenia: a cross-sectional study in first-episode and
chronic illness. Br J Psychiatry. 2008; 192: 429–434.
- [30] Downhill Jr J.E, Buchsbaum MS, Wei T, Spiegel-Cohen J, Hazlett
EA, Haznedar MM, et al. Shape and size of the corpus callosum
in schizophrenia and schizotypal personality disorder.
Schizophr. Res. 2000; 42: 193–208.
- [31] Rotarska-Jagiela A, Schönmeyer R, Oertel V, Haenschel C,
Vogeley K, Linden DE.. The corpus callosum in schizophrenia volume and connectivity changes affect specific regions. NeuroImage 2008; 39: 1522–1532.
- [32] Whitford TJ, Kubicki M, Schneiderman JS, O’Donnell LJ, King
R, Alvarado JL, et al. Corpus Callosum Abnormalities and
their Association with Psychotic Symptoms in Patients with
Schizophrenia. Biol. Psychiatry. 2010; 68:70–77