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Hippocampal volume asymmetry and age at illness onset in males with schizophrenia

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Abstract

To determine whether there are disturbances of hippocampal volume asymmetry in schizophrenic patients, we obtained contiguous, I-mm-thick magnetic resonance images in 28 males with chronic schizophrenia and in 28 age-matched healthy males. The schizophrenic patients showed a bilateral reduction in volume of the hippocampal formation (HF; left 7.0%; right 8.7%). This reduction was significantly associated with the severity of disorganization syndrome (P < 0.0005). A significant asymmetry in the HF volume was found in the control subjects (P = 0.006), but not in the patients (P = 0.40). There was a significant positive correlation between the asymmetry index and the patient’s age at the onset of schizophrenia (r = 0.46,P = 0.01). Results indicate that a disturbance in the normal asymmetry of the HF may be a characteristic in schizophrenia, particularly in patients with an early onset of the illness.

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References

  • Adam C, Baulac M, Saint-Hilaire J-M, Laudau J, Granat O, Laplane D (1994) Value of magnetic resonance imaging-based measurements of hippocampal formations in patients with partial epilepsy. Arch Neurol 51:130–138

    PubMed  CAS  Google Scholar 

  • American Psychiatric Association (1987) Diagnostic and statistical manual of mental disorders (DSM-III-R), 3rd edn revised. American Psychiatric Press, Washington, DC

    Google Scholar 

  • Andreasen NC (1984a) Scale for the Assessment of Negative Symptoms (SANS). University of Iowa, Iowa City

    Google Scholar 

  • Andreasen NC (1984b) Scale for the Assessment of Positive Symptoms (SAPS). University of Iowa, Iowa City

    Google Scholar 

  • Becker T, Elmer K, Mechela B, Schneider F, Taubert F, Schroth G, Grodd W, Bartels M, Beckmann H (1990) MRI findings in medial lobe structures in schizophrenia. Eur Neuropsychopharmacol 1: 83–86

    Article  PubMed  CAS  Google Scholar 

  • Berger TW, Berry SD, Thompson RF (1986) Role of the hippocampus in classical conditioning of aversive and apperitive behaviors. In: Isaacson RL, Pribram KH (eds) The hippocampus, vol 4. Plenum Press, New York, pp 203–240

    Google Scholar 

  • Bilder RM, Wu H, Bogerts B, DeGreef G, Ashtari M, Alvir JMJ, Snyder PJ, Lieberman JA (1994) Absence of regional hemispheric volume asymmetries in first-episode schizophrenia. Am J Psychiatr 151:1437–1447

    PubMed  CAS  Google Scholar 

  • Bogerts B (1991) The neuropathology of schizophrenia: pathophysiological and neurodevelopmental implications. In: Mednic SA, Cannon TD, Barr CE (eds) Fetal neural development and adult schizophrenia. Cambridge University Press, Cambridge, pp 153–173

    Google Scholar 

  • Chua SE, McKenna PJ (1995) Schizophrenia: a brain disease? A critical review of structural and functional cerebral abnormality in the disorder. Br J Psychiatry 166:563–582

    PubMed  CAS  Google Scholar 

  • Cook MJ, Fish DR, Shorvon SD, Straughan K, Stevens JM (1992) Hippocampal volumetric and morphometric studies in frontal and temporal lobe epilepsy. Brain 115: 1001–1015

    Article  PubMed  Google Scholar 

  • Crow TJ (1990) Temporal lobe asymmetries as the key to the etiology of schizophrenia. Schizophr Bull 16:433–443

    PubMed  CAS  Google Scholar 

  • Eichenbaum H, Wiener SI, Shapiro ML, Cohen NJ (1989) The organization of spatial coding in the hippocampus: a study of neural ensemble activity. J Neurosci 9:2764–2775

    PubMed  CAS  Google Scholar 

  • Falkai P, Bogerts B, Schneider T, Greve B, Pfeiffer U, Machus B, Fölsch-Reetz B, Majtenyi C, Ovary I (1992) Loss of sylvian fissure asymmetry in schizophrenia: a quantitative postmortem study. Schizophr Res 7:23–32

    Article  PubMed  CAS  Google Scholar 

  • Fukuzako H, Fukuzako T, Hashiguchi T, Hokazono Y, Takeuchi K, Hirakawa K, Ueyama K, Takigawa M, Kajiya Y, Nakajo M, Fujimoto T (1996) Reduction in hippocampal formation volume is caused mainly by its shortening in chronic schizophrenia: assessment by MRI. Biol Psychiatry 39:938–945

    Article  PubMed  CAS  Google Scholar 

  • Gabriel M, Sparenborg S, Stolar N (1986) An executive function of the hippocampus: pathway selection for thalamic neuronal significance code. In: Isaacson RL, Pribram KH (eds) The hippocampus, vol 4. Plenum Press, New York, pp 1–40

    Google Scholar 

  • Gilmore RL, Childress MD, Leonard C, Quisling R, Roper S, Eisenschenk S, Mahoney M (1995) Hippocampal volumetrics differentiate patients with temporal lobe epilepsy and extratemporal lobe epilepsy. Arch Neurol 52:819–824

    PubMed  CAS  Google Scholar 

  • Jack CR Jr, Twomey CK, Zinsmeister AR, Sharbrough FW, Petersen RC, Cascino GD (1989) Anterior temporal lobes and hippocampal formations: normative volumetric measurements from MR images in young adults. Radiology 172:549–554

    PubMed  Google Scholar 

  • Jacobsen LK, Giedd IN, Vaituzis AC, Hamburger SD, Rajapakse JC, Frazier JA, Kaysen D, Lenane MC, McKenna K, Gordon CT, Rapoport JL (1996) Temporal lobe morphology in childhood-onset schizophrenia. Am J Psychiatry 153:355–361

    PubMed  CAS  Google Scholar 

  • Joseph R (1992) The limbic system: emotion, laterality, and unconscious mind. Psychoanal Rev 79:405–456

    PubMed  CAS  Google Scholar 

  • Liddle PF, Barnes THE (1990) Syndromes of chronic schizophrenia. Br J Psychiatry 157:558–561

    Article  PubMed  CAS  Google Scholar 

  • Olton DS, Wible CG, Shapiro ML (1986) Mnemonic theories of hippocampal function. Behav Neurosci 100: 852–857

    Article  PubMed  CAS  Google Scholar 

  • Petty RG, Barta PE, Pearlson GD, McGilchrist IK, Lewis RW, Tien AY, Pulver A, Vaughn DD, Casanova MF, Powers RE (1995) Reversal of asymmetry of the planum temporale in schizophrenia. Am J Psychiatry 152:715–721

    PubMed  CAS  Google Scholar 

  • Pribram KH (1986) The hippocampal system and recombinant processing. In: Isaacson RL, Pribram KH (eds) The hippocampus, vol 4. Plenum Press, New York, pp 329–370

    Google Scholar 

  • Schachter SC, Ransil BJ, Geschwind N (1987) Associations of handedness with hair color and learning disabilities. Neuropsychologia 25:269–276

    Article  PubMed  CAS  Google Scholar 

  • Soininnen HS, Partanen K, Pitkanen A, Vainio P, Hanninen T, Hallikainen M, Koivisto K, Riekkinen PJ (1994) Volumetric MRI analysis of the amygdala and the hippocampus in subjects with age-associated memory impairment: correlation to visual and verbal memory. Neurology 44:1660–1668

    Google Scholar 

  • Squire LR, Zola-Morgan S (1991) The medial temporal lobe memory system. Science 253:1380–1386

    Article  PubMed  CAS  Google Scholar 

  • Stevens JR (1986) Clinicopathologic correlations in schizophrenia. Arch Gen Psychiatry 43:715–716

    PubMed  CAS  Google Scholar 

  • Torrey EF, Peterson MR (1974) Schizophrenia and the limbic system. Lancet II: 942–946

    Google Scholar 

  • Weinberger DR (1995) Neurodevelopmental perspectives on schizophrenia. In: Bloom FE, Kupfer DJ (eds) Psychopharmacology: the fourth generation of progress. Raven Press, New York, pp 1171–1183

    Google Scholar 

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Fukuzako, H., Yamada, K., Kodama, S. et al. Hippocampal volume asymmetry and age at illness onset in males with schizophrenia. Eur Arch Psychiatry Clin Nuerosci 247, 248–251 (1997). https://doi.org/10.1007/BF02900302

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