Literature DB >> 24090512

Eyeblink conditioning in unmedicated schizophrenia patients: a positron emission tomography study.

Krystal L Parker1, Nancy C Andreasen, Dawei Liu, John H Freeman, Daniel S O'Leary.   

Abstract

Previous studies suggest that patients with schizophrenia exhibit dysfunctions in a widely distributed circuit-the cortico-cerebellar-thalamic-cortical circuit, or CCTCC-and that this may explain the multiple cognitive deficits observed in the disorder. This study uses positron emission tomography (PET) with O(15) H₂O to measure regional cerebral blood flow (rCBF) in response to a classic test of cerebellar function, the associative learning that occurs during eyeblink conditioning, in a sample of 20 unmedicated schizophrenia patients and 20 closely matched healthy controls. The PET paradigm examined three phases of acquisition and extinction (early, middle and late). The patients displayed impaired behavioral performance during both acquisition and extinction. The imaging data indicate that, compared to the control subjects, the patients displayed decreases in rCBF in all three components of the CCTCC during both acquisition and extinction. Specifically, patients had less rCBF in the middle and medial frontal lobes, anterior cerebellar lobules I/V and VI, as well as the thalamus during acquisition and although similar areas were found in the frontal lobe, ipsilateral cerebellar lobule IX showed consistently less activity in patients during extinction. Thus this study provides additional support for the hypothesis that patients with schizophrenia have a cognitive dysmetria--an inability to smoothly coordinate many different types of mental activity--that affects even a very basic cognitive task that taps into associative learning.
© 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Cerebellum; Cognitive dysmetria; Eyeblink; Positron emissions tomography (PET); Schizophrenia

Mesh:

Year:  2013        PMID: 24090512      PMCID: PMC3980571          DOI: 10.1016/j.pscychresns.2013.07.006

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  40 in total

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