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Reduced Cognitive Control of a Visually Bistable Image in Schizophrenia

Published online by Cambridge University Press:  09 March 2011

Ryan McBain*
Affiliation:
Mailman Research Center, McLean Hospital, Belmont, Massachusetts
Daniel J. Norton
Affiliation:
Department of Psychology, Boston University, Boston, Massachusetts
Jejoong Kim
Affiliation:
Department of Brain and Cognitive Sciences, Seoul National University, Seoul, Korea
Yue Chen
Affiliation:
Mailman Research Center, McLean Hospital, Belmont, Massachusetts Department of Psychiatry, Harvard Medical School, Boston, Massachusetts
*
Correspondence and reprint requests to: Ryan McBain, McLean Hospital, 115 Mill Street, Belmont, MA, 02478. E-mail: [email protected]

Abstract

Schizophrenia is associated with the inability to control and coordinate thoughts, actions, and perceptions. In conventional assessments of cognitive control, multiple sensory features of stimuli are concomitantly manipulated, introducing a confounding role of bottom-up perceptual information. To overcome this difficulty, we used an ambiguous visual stimulus (Necker cube), which allowed measurement of cognitive control with constant sensory input. Subjects (20 patients, 20 controls) were asked to control their perception of a transparent Necker cube by keeping a designated plane at the front or back of the stimulus, the position of which is perceptually bistable. Patients were highly deficient at controlling their perception of the cube. When a visual feature (the luminance contrast between a designated cube plane and the other planes) was systematically manipulated, an interaction was found whereby schizophrenia patients no longer under-performed on the highest contrast condition. These results show patients’ impairment of controlling perception in the absence of visual modulation and suggest the potential utility of perceptually based approaches to cognitive remediation in schizophrenia. (JINS, 2011, 551–556)

Type
Brief Communications
Copyright
Copyright © The International Neuropsychological Society 2011

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References

Barrett, S.L., Mulholland, C.C., Cooper, S.J., Rushe, T.M. (2009). Patterns of neurocognitive impairment in first-episode bipolar disorder and schizophrenia. British Journal of Psychiatry, 195, 6772.CrossRefGoogle Scholar
Butler, P.D., Javitt, D.C. (2005). Early-stage visual processing deficits in schizophrenia. Current Opinions in Psychiatry, 18, 151157.CrossRefGoogle ScholarPubMed
Butler, P.D., Schechter, I., Zemon, V., Schwartz, S.G., Greenstein, V.C., Gordon, J., Javitts, D. (2001) (Dysfunction of early-stage visual processing in schizophrenia. American Journal of Psychiatry, 158, 11261133.CrossRefGoogle ScholarPubMed
Chen, Y., Levy, D.L., Nakayama, K., Matthysse, S., Palafox, G., Holzman, P.S. (1999). Dependence of impaired eye tracking on deficient velocity discrimination in schizophrenia. Archives of General Psychiatry, 56, 155161.CrossRefGoogle ScholarPubMed
Chen, Y., Nakayama, K., Levy, D.L., Matthysse, S., Holzman, P.S. (1999). Psychophysical isolation of a motion-processing deficit in schizophrenics and their relatives and its association with impaired smooth pursuit. Proceedings of the National Academy of Sciences of the United States of America, 96, 47244729.CrossRefGoogle ScholarPubMed
Chen, Y., Norton, D., McBain, R. (2008). Can persons with schizophrenia appreciate visual art? Schizophrenia Research, 105, 245251.CrossRefGoogle ScholarPubMed
Chen, Y., Palafox, G.P., Nakayama, K., Levy, D.L., Matthysse, S., Holzman, P.S. (1999). Motion perception in schizophrenia. Archives of General Psychiatry, 56, 149154.CrossRefGoogle ScholarPubMed
Danckert, J., Saoud, M., Maruff, P. (2004). Attention, motor control and motor imagery in schizophrenia: implications for the role of the parietal cortex. Schizophrenia Research, 70, 241261.CrossRefGoogle ScholarPubMed
First, M.B., Spitzer, R.L., Gibbon, M., Williams, J.B. (2002). Structured clinical interview for DSM-IV-TR axis I disorders -patient edition (SCID—I/P, 11/2002 revision). New York, NY: Biometrics Research Department.Google Scholar
Fisher, M., Holland, C., Merzenich, M.M., Vinogradov, S. (2009). Using neuroplasticity-based auditory training to improve verbal memory in schizophrenia. American Journal of Psychiatry, 166, 805811.CrossRefGoogle ScholarPubMed
Gold, J.M., Fuller, R.L., Robinson, B.M., Braun, E.L., Luck, S.J. (2007). Impaired top-down control of visual search in schizophrenia. Schizophrenia Research, 94, 148155.CrossRefGoogle ScholarPubMed
Green, M.F., Butler, P.D., Chen, Y., Geyer, M.A., Silverstein, S., Wynn, J.K., Zemon, V. (2009) (Perception measurement in clinical trials of schizophrenia: promising paradigms from CNTRICS. Schizophrenia Bulletin, 35, 163181.CrossRefGoogle ScholarPubMed
Henik, A., Salo, R. (2004). Schizophrenia and the Stroop effect. Behavioral and Cognitive Neuroscience Reviews, 3, 4259.CrossRefGoogle ScholarPubMed
Hugdahl, K. (2009). “Hearing voices”: auditory hallucinations as failure of top-down control of bottom-up perceptual processes. Scandinavian Journal of Psychology, 50, 553560.CrossRefGoogle ScholarPubMed
Hugdahl, K., Løberg, E.M., Jørgensen, H.A., Lundervold, A., Lund, A., Green, M.F., Rund, B.R. (2008). Left hemisphere lateralization of auditory hallucinations in schizophrenia: a dichotic listening study. Cognitive Neuropsychiatry, 13, 166179.CrossRefGoogle ScholarPubMed
Hugdahl, K., Rund, B.R., Lund, A., Asbjornsen, A., Egeland, J., Landro, N.I., Sundet, K. (2003) (Attention and executive dysfunctions in schizophrenia and depression: evidence from dichotic listening performance. Biological Psychiatry, 53, 609616.CrossRefGoogle ScholarPubMed
Joyce, E., Hutton, S., Mutsatsa, S., Gibbins, H., Webb, E., Paul, S., Barnes, T. (2002) (Executive dysfunction in first-episode schizophrenia and relationship to duration of untreated psychosis: the West London Study. British Journal of Psychiatry Supplement, 43, s38s44.CrossRefGoogle ScholarPubMed
Kay, S.R., Fiszbein, A., Opler, L.A. (1987). The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophrenia Bulletin, 13(2), 261276.CrossRefGoogle ScholarPubMed
Kim, J.J., Park, H.J., Jung, Y.C., Chun, J.W., Kim, H.S., Seok, J.H., Lee, J.D. (2009) (Evaluative processing of ambivalent stimuli in patients with schizophrenia and depression: a [150] H20 PET study. Journal of the International Neuropsychological Society, 15, 9901001.CrossRefGoogle Scholar
McBain, R., Norton, D., Chen, Y. (2010). Differential roles of low and high spatial frequency contents in abnormal facial emotion perception in schizophrenia. Schizophrenia Research, 122, 151155.CrossRefGoogle ScholarPubMed
Nuechterlein, K.H., Luck, S.J., Lustig, C., Sarter, M. (2009). CNTRICS final task selection: control of attention. Schizophrenia Bulletin, 35(1), 182196.CrossRefGoogle ScholarPubMed
O'Leary, D.S. (2003). Effects of attention on hemispheric asymmetry. Cambridge, MA: MIT Press.Google Scholar
Peterson, M.A., Hochberg, J. (1983). Opposed-set measurement procedure: a quantitative analysis of the role of local cues and intention in form perception. Journal of Experimental Psychology: Human Performance and Perception, 9, 183193.Google Scholar
Sereno, A.B., Holzman, P.S. (1996). Spatial selective attention in schizophrenic, affective disorder, and normal subjects. Schizophrenia Research, 20(1–2), 3350.CrossRefGoogle ScholarPubMed
Slotnick, S.D., Yantis, S. (2005). Common neural substrates for the control and effects of visual attention and perceptual bistability. Brain research. Cognitive Brain Research, 24, 97108.CrossRefGoogle ScholarPubMed
Wechsler, D. (1981). Manual for the adult intelligence scale-revised. New York: Psychological Corporation.Google Scholar