Literature DB >> 10456801

High velocity transient visual processing deficits diminish ability of patients with schizophrenia to recognize objects.

B D Schwartz1, B A Maron, W J Evans, D K Winstead.   

Abstract

OBJECTIVE: Early information processing deficits are consistently reported for patients with schizophrenia. A growing number of studies have applied a transient (magnocellular) or sustained (parvocellular) explanation to account for deficient processing of briefly presented visual stimuli, moving stimuli, and stimuli requiring eye movements in patients with schizophrenia. This reasoning is based on research that makes the distinction between a magnocellular channel, which primarily responds to low spatial frequency and moving or rapidly presented visual information, and a parvocellular channel, which is primarily responsive to high spatial frequency and detailed information.
BACKGROUND: Although the preponderance of findings offer support for transient ("where is it") as opposed to sustained ("what is it") deficit in patients with schizophrenia, there remains a need for more specific depiction of the deficit.
METHOD: The present study evaluated normal control subjects and patients with schizophrenia recruited from in-patient and out-patient settings. A Motion Defined Letter task was used, owing to its sensitivity to transient (magnocellular) activation.
RESULTS: Twenty-three patients with schizophrenia and sixteen normal control subjects were tested on eight dot velocity levels, ranging from 88 arc min/sec to 0.69 arc min/sec. A repeated measures analysis of variance indicated that the performance of patients with schizophrenia was significantly poorer than that of their normal counterparts on the three fastest dot velocity conditions (88 arc min/sec, p < 0.0001, 44 arc min/sec, p < 0.00001, and 22 arc min/sec, p < 0.00003), but performance did not differ on the five slower dot velocity conditions. A regression analysis revealed that the dosage of medication was positively associated with performance on three middle range dot velocity conditions (11 arc min/sec F (1,22) = 6.99; p < 0.025; 5.5 arc min/sec, F (2,20) = 0.379; p = 0.05, and 2.25 arc min/sec F (2,20) = 7.37; p < 0.005).
CONCLUSIONS: The findings afford support for an early information processing deficit in schizophrenics. These data also support the neurophysiologic model that explains the poor performance of patients with schizophrenia as it relates to a transient channel deficiency.

Entities:  

Mesh:

Year:  1999        PMID: 10456801

Source DB:  PubMed          Journal:  Neuropsychiatry Neuropsychol Behav Neurol        ISSN: 0894-878X


  13 in total

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2.  A new dimension of sensory dysfunction: stereopsis deficits in schizophrenia.

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Review 3.  [One decade of functional imaging in schizophrenia research. From visualisation of basic information processing steps to molecular-genetic oriented imaging].

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4.  Magnocellular contributions to impaired motion processing in schizophrenia.

Authors:  Dongsoo Kim; Glenn Wylie; Roey Pasternak; Pamela D Butler; Daniel C Javitt
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5.  Eye movement and visual motion perception in schizophrenia II: Global coherent motion as a function of target velocity and stimulus density.

Authors:  Walter L Slaghuis; Tina Holthouse; Amy Hawkes; Raimondo Bruno
Journal:  Exp Brain Res       Date:  2007-06-14       Impact factor: 1.972

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7.  Impaired early visual response modulations to spatial information in chronic schizophrenia.

Authors:  Jean-François Knebel; Daniel C Javitt; Micah M Murray
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8.  Early-stage visual processing and cortical amplification deficits in schizophrenia.

Authors:  Pamela D Butler; Vance Zemon; Isaac Schechter; Alice M Saperstein; Matthew J Hoptman; Kelvin O Lim; Nadine Revheim; Gail Silipo; Daniel C Javitt
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9.  Subcortical visual dysfunction in schizophrenia drives secondary cortical impairments.

Authors:  Pamela D Butler; Antigona Martinez; John J Foxe; Dongsoo Kim; Vance Zemon; Gail Silipo; Jeannette Mahoney; Marina Shpaner; Maria Jalbrzikowski; Daniel C Javitt
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10.  Impairments in generation of early-stage transient visual evoked potentials to magno- and parvocellular-selective stimuli in schizophrenia.

Authors:  Isaac Schechter; Pamela D Butler; Vance M Zemon; Nadine Revheim; Alice M Saperstein; Maria Jalbrzikowski; Roey Pasternak; Gail Silipo; Daniel C Javitt
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