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Estructura y función del cuerpo calloso en la esquizofrenia: ¿Cuál es la conexión?

Published online by Cambridge University Press:  12 May 2020

A. S. David
Affiliation:
Departamento de Medicina Psicológica, King's College Hospital e Instituto de Psiquiatría, Londres
C. Minne
Affiliation:
Hospital Maudsley, Londres
P. Jones
Affiliation:
Departamento de Medicina Psicológica, King's College Hospital e Instituto de Psiquiatría, Londres
I. Harvey
Affiliation:
Departamento de Medicina Psicológica, King's College Hospital e Instituto de Psiquiatría, Londres Hospital Maudsley, Londres
M. A. Ron
Affiliation:
Instituto de Neurología, Queen Square, Londres, Reino Unido
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Resumen

Estudios de la estructura y función del cuerpo calloso han revelado anormalidades en pacientes esquizofrénicos. Una prueba funcional de este tipo empleó estímulos de Stroop lateralizados presentados taquistoscópicamente para medir la transferencia de interferencia y facilitación entre los hemisferios cerebrales. Se hizo un intento de relacionar índices de transferencia del cuerpo calloso con variables clínicas y demográficas, incluida la historia familiar, y con índices de morfología cerebral. Los últimos incluían la razón ventrículoxerebro (RVC) medida por tomografía computarizada (TC) en 31 esquizofrénicos según el DSMIII, y el área transversal del cuerpo calloso a partir de imágenes de resonancia magnética (IRM), obtenidas de 20 de estos pacientes. La RVC no estaba relacionada con medidas funcionales; sin embargo, el área anterior del cuerpo calloso tenía correlación con índices de conectividad del cuerpo calloso. Los pacientes con alucinaciones auditivas tenían el área anterior del cuerpo calloso más pequeña y tendían a mostrar menos conectividad. Los resultados muestran relaciones entre medidas funcionales y estructurales del cuerpo calloso, pero su naturaleza precisa es poco clara.

Type
Artículo original
Copyright
Copyright © European Psychiatric Association 1995

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References

Bibliografía

American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition. Washington DC: American Psychiatric Association, 1987.Google Scholar
Annett, M. A classification of hand preference by association analysis. Br J Psychol 1970; 61: 303-21.CrossRefGoogle ScholarPubMed
Barta, PE, Pearlson, GD, Powers, REet al. Auditory hallucinations and smaller superior temporal gyral volume in schizophrenia. Am J Psychiatry 1990; 147: 1457-62.Google Scholar
Beaumont, JG, Dimond, SJ. Brain disconnection and schizophrenia. Br J Psychiatry 1973; 123: 661-2.10.1192/bjp.123.6.661CrossRefGoogle Scholar
Bech, P, Kastrup, M, Rafaelsen, OJ. Mini-compendium of rating scales for States of anxiety, depression, mania and schizophrenia with corresponding DSMIII syndromes. Acta Psychiatr Scand 1986; 73 (suppl 326): 32-7.Google Scholar
Benson, DF, Zaidel, E. The Dual Brain. New York: Guilford Press, 1985.Google Scholar
Bigelow, LB, Nasrallah, HA, Rauscher, FP. Corpus callosum thickness in chronic schizophrenia. Br J Psychiatry 1983; 142: 284-7.CrossRefGoogle ScholarPubMed
Casanova, MF, Sanders, RD, Goldberg, TEet al. Morphometry of the corpus callosum in monozygotic twins discordant for schizophrenia: a magnetic resonance imaging study. J Neurol Neurosurg Psychiatry 1990; 53: 416-21.CrossRefGoogle ScholarPubMed
Clarke, JM, Lufkin, RB, Zaidel, E. Corpus callosum morphometry and dichotic listening performance: individual differences in functional interhemispheric inhibition. Neuropsychologia 1993; 31: 547-57.10.1016/0028-3932(93)90051-ZCrossRefGoogle ScholarPubMed
Clarke, S, Kraftsik, R, Van der Loos, Het al. Forms and measures of adult and developing human corpus callosum: Is there sexual dimorphism? J Comp Neurol 1989; 280: 213-30.Google Scholar
Cleghorn, JM, Franco, S, Szechtman, Bet al. Toward a brain map of auditory hallucinations. Am J Psychiatry 1992; 149:1062-9.Google Scholar
Coger, RW, Serafetinides, EA. Schizophrenia, corpus callosum, and interhemispheric communication: a review. Psychiatry Res 1990; 34: 163-84.CrossRefGoogle ScholarPubMed
Cook ND. The Brain Code: Mechanisms of Information Transfer and the Role of the Corpus Callosum. London: Methuen, 1986.Google Scholar
David, AS. Tachistoscopic tests of colour naming and matching in schizophrenia: evidence for posterior callosum dysfunction? Psychol Med 1987; 17: 621-30.10.1017/S0033291700025861CrossRefGoogle ScholarPubMed
David, AS. Stroop interference within and between the cerebral hemispheres: studies in normals and acallosals. Neuropsychologia 1992; 30: 161-75.CrossRefGoogle ScholarPubMed
David, AS. Callosal transfer in schizophrenia: too much or too little? J Abnorm Psychol 1993; 102: 573-9.10.1037/0021-843X.102.4.573CrossRefGoogle ScholarPubMed
David, AS, Wacharasindhu, A, Lishman, WA. Developmental abnormalities of the corpus callosum and severe psychiatric disorders: review and case series. J Neurol Neurosurg Psychiatry 1993; 56: 8593.CrossRefGoogle ScholarPubMed
DeLisi, LE, Hoff, AL, Schwartz, JEet al. Brain morphology in first-episode schizophrenic-like psychotic patients: a quantitative magnetic resonance imaging study. Biol Psychiatry 1991; 29: 159-75.CrossRefGoogle ScholarPubMed
S, DemeterRingo, JL, Doty, RW. Morphometric analysis of the human corpus callosum and anterior commissure. Hum Neurobiol 1988; 6: 219-26.Google Scholar
Doty, RW. Schizophrenia: a disease of interhemispheric processes at forebrain and brainstem levels? Behav Brain Res 1989; 34: 133.CrossRefGoogle ScholarPubMed
Dyer, FN. Interference and facilitation for color naming with separate bilateral presentations of the word and color. J Exp Psychol 1973; 99: 314-7.CrossRefGoogle Scholar
Green, P, Hallet, S, Hunter, M. Abnormal interhemisp-heric integration and hemisphere specialization in schizophrenics and high-risk children. In: Gruzelier, JH, Flor Henry, P, eds. Laterality and Psychopathology. Amsterdam: Elsevier Science Publishers, 1986; 443-70.Google Scholar
Günther, W, Petsch, R, Steinberg, Ret al. Brain dysfunction during motor activation and corpus ca llosum alterations in schizophrenia measured by cerebral blood flow and magnetic resonance imaging. Biol Psychiatry 1991; 29: 535-55.CrossRefGoogle Scholar
Habib, M, Gayraud, D, Oliva, Aet al. Effects of han dedness and sex on the morphology of the corpus callosum: a study with brain magnetic resonance imaging. Brain Cognition 1991; 16: 4161.10.1016/0278-2626(91)90084-LCrossRefGoogle Scholar
Harvey, I, McGuffin, P, Williams, M, Toone, BK. The ventriclebrain ration infunctional psychoses: an admixture analysis. Psychiatr Res 1990; 35: 619.CrossRefGoogle Scholar
Harvey, I, Ron, MA, Murray, R, Lewis, S, Barker, G, McManus, D. MRI in schizophrenia: basal ganglia and white matter T1 times. Psychol Med 1991; 21: 587-98.CrossRefGoogle ScholarPubMed
Harvey, I, Ron, MA, du Boulay, G, Wicks, D, Lewis, SW, Feinstein, A, Murray, R. Reduction of cortical volunte in schizophrenia on magnetic resonance imaging. Psychol Med 1992; 23: 591604.CrossRefGoogle Scholar
Johnstone, EC, Crow, TJ, Frith, CD, Husband, J, Kreel, L. Cerebral ventricular size and cognitive impair ment in chronic schizophrenia. Lancet 1976; ii: 92-46.Google Scholar
MacLeod, CM. Half a century of research on the Stroop effect: an integrative review. Psychol Bull 1991; 109: 163203.10.1037/0033-2909.109.2.163CrossRefGoogle Scholar
McKeever, WF, Jackson, TL. Cerebral dominance as sesséd by object and colournaming latencies: sex and familial sinistrality effects. Brain Land 1979; 7: 175-90.CrossRefGoogle Scholar
McManus, DG, Kermode, AG, Tofts, PS. A repositio ning technique for cerebral magnetic resonance imaging of patients with múltiple sclerosois. Society of Magnetic Resonance in Medicine, abstracts (vol. 2) of the 8th annual meeting, Amsterdam, 1989; 617.Google Scholar
Nasrallah, HA. The unintegrated right cerebral he mispheric consciousness as alien intruder. Compr Psychiatry 1985; 26: 273-82.CrossRefGoogle Scholar
Nasrallah, HA, Andreasen, NC, Coffman, JAet al. A controlled magnetic resonance imaging study of corpus callosum in schizophrenia. Biol Psychiatry 1986; 21: 274-82.CrossRefGoogle Scholar
Nasrallah, HA, Andreasen, NC, Coffman, JAet al. A controlled magnetic resonance imaging study of corpus callosum in schizophrenia. Biol Psychiatry 1986; 21: 274-82.CrossRefGoogle Scholar
Nelson, HE, O’Connell, NA. Dementia: the estimation of premorbid intelligence levels using the new adult reading test. Cortex 1978; 14: 234-44.CrossRefGoogle ScholarPubMed
Oepen, G, Füngeld, M, Höll, Tet al. Schizophrenia an emotional hypersensitivity of the right cerebral hemisphere. Int J Psychophysiol 1987; 5: 261-4.CrossRefGoogle ScholarPubMed
O’Kusky, J, Strauss, E, Kosaka, Bet al. The corpus callosum is larger with righthemisphere cebral dominance. Ann Neurol 1988; 24: 379-83.CrossRefGoogle Scholar
Raine, A, Harrison, GN, Reynolds, GPet al. Structural and functional characteristics of the corpus callosum in schizophrenics, psychiatric Controls, and normal Controls. Arch Gen Psychiatry 1990; 47: 1060-4.CrossRefGoogle ScholarPubMed
Randall, PL. Schizophrenia, abnormal connection and brain evolution. Med Hypotheses 1983; 10: 247-80.CrossRefGoogle ScholarPubMed
Robb, RA, Barillot, C. Interactive display and analysis of 3D medical images. IEEE Trans Med Imaging 1989; 8: 217-26.CrossRefGoogle Scholar
Rosenthal, R, Bigelow, LB. Quantitative brain measu res in chronic schizophrenia. Br J Psychiatry 1972; 121: 259-64.CrossRefGoogle Scholar
Schneider, K. Clinical Psychopathology. New York: Grune and Stratton, 1959.Google Scholar
Schwarzkopf, SB, Nasrallah, HA, Olson, SCet al. Family history and brain morphology in schizophrenia: an MRI study. Psychiatr Res Neuroimaging 1991; 40: 4960.CrossRefGoogle Scholar
Swayze, VW, Andreasen, NC, Ehrhardt, JC, Yoh, WTC, Alliger, RJ, Cohen, GA. Developmental abnormalities of the corpus callosum in schizophrenia. Arch Neurol 1990; 47: 805-8.CrossRefGoogle Scholar
Wing, JK, Cooper, JE, Sartorius, N. Measurement and Classification of Psychiatric Symptoms. Cambridge: Cambridge University Press, 1974.Google Scholar
Uematsu, M, Kaiya, H. The morphology of the corpus callosum in schizophrenia. An MRI study. Schi zophr Res 1988; 1: 391-8.CrossRefGoogle ScholarPubMed
Witelson, SF. Hand and sex differences in the isthmus and genu of the human corpus callosum: a postmor tem morphological study. Brain 1989; 112: 799835.CrossRefGoogle Scholar
Woodruff, PWR, Pearlson, GD, Geer, MJ, Barta, PE, Chilcoat, HD. A computerized magnetic resonance imaging of corpus callosum morphology in schizophrenia. Psychol Med 1993; 23: 4556.CrossRefGoogle Scholar
Young, AW. Mthodological and theoretical bases. In: Beaumont, JG, ed. Divided Visual Field Studies of Cerebral Organisation. London: Academic Press, 1982.Google Scholar
Zaidel, E, Clarke, JM, Suyenobu, B. Hemispheric inde pendence: a paradigm case for cognitive neuroscience. In: Scheibel, A, Weschler, A, ess. Neurobiology of Higher Cognitive Functioning. New York: Guilford Press, 1990.Google Scholar