Changes in the visual-evoked P1 potential as a function of schizotypy and background color in healthy young adults

Journal of Psychiatric Research

Volumn 47, Issue 4, 2013, Pages 542-547

  Bedwell, Jeffrey S ^a   Chan, Chi C ^a   Trachik, Benjamin J ^a   Rassovsky, Yuri ^b,c  

^a UNIVERSITY OF CENTRAL FLORIDA   (United States)

^b BAR ILAN UNIVERSITY   (Israel)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Electroencephalography; Evoked response potentials; Magnocellular visual pathway; Schizophrenia; Schizotypal personality disorder; Schizotypy

Indexed keywords

ADULT; ARTICLE; COLOR; EVOKED VISUAL RESPONSE; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; HUMAN EXPERIMENT; MAGIC; MALE; NORMAL HUMAN; PRIORITY JOURNAL; RED LIGHT; RIGHT HEMISPHERE; SCHIZOPHRENIA; SCHIZOTYPAL PERSONALITY DISORDER; SCHIZOTYPAL PERSONALITY QUESTIONNAIRE; SYMPTOM; UNDERGRADUATE STUDENT; WHITE LIGHT;

EID: 84874444569     PISSN: 00223956     EISSN: 18791379     Source Type: Journal    
DOI: 10.1016/j.jpsychires.2012.12.012     Document Type: Article

References (41)

1. Asai T., Sugimori E., Bando N., Tanno Y. The hierarchic structure in schizotypy and the five-factor model of personality. Psychiatry Research 2011, 185(1-2):78-83.
2. Barbato M., Collinson S.L., Casagrande M. Altered depth perception is associated with presence of schizotypal personality traits. Cognitive Neuropsychiatry 2012, 17(2):115-132.
3. Bedwell J.S., Brown J.M., Orem D.M. The effect of a red background on location backward masking by structure. Perception and Psychophysics 2008, 70:503-507.
4. Bedwell J.S., Brown J.M., Yanasak N.E., Miller L.S. Schizophrenia and red light: fMRI evidence for a novel biobehavioral marker. International Journal of Neuroscience 2006, 116:881-894.
5. Bedwell J.S., Hernandez D.C., Ranieri A.Y. The backward masking red light effect and schizotypy: the influence of sex. Psychiatry Research 2011, 189(2):228-232.
6. Bedwell J.S., Orem D.M. The effect of red light on backward masking in individuals with psychometrically defined schizotypy. Cognitive Neuropsychiatry 2008, 13(6):491-504.
7. Bedwell J.S., Orem D.M., Rassovsky Y., Allen L.G., Sutterby S.R. A potential qualitative endophenotype for schizophrenia: backward masking response to red light. Psychiatry Research 2009, 166(2-3):166-173.
8. Bedwell J.S., Rassovsky Y., Orem D.M., Kamath V. The backward masking red light effect in schizophrenia: relationship to clinical features and neurocognitive performance. Journal of Abnormal Psychology 2011, 120(2):490-496.
9. Breitmeyer B.G., Williams M.C. Effects of isoluminant-background color on metacontrast and stroboscopic motion: Interactions between sustained (p) and transient (m) channels. Vision Research 1990, 30:1069-1075.
10. Butler P.D., Martinez A., Foxe J.J., Kim D., Zemon V., Silipo G., et al. Subcortical visual dysfunction in schizophrenia drives secondary cortical impairments. Brain: A Journal of Neurology 2007, 130(Pt 2):417-430.
11. Butler P.D., Schechter I., Zemon V., Schwartz S.G., Greenstein V.C., Gordon J., et al. Dysfunction of early-stage visual processing in schizophrenia. American Journal of Psychiatry 2001, 158(7):1126-1133.
12. Butler P.D., Zemon V., Schechter I., Saperstein A.M., Hoptman M.J., Lim K.O., et al. Early-stage visual processing and cortical amplification deficits in schizophrenia. Archives of General Psychiatry 2005, 62(5):495-504.
13. Chapman C., Hoag R., Giaschi D. The effect of disrupting the human magnocellular pathway on global motion perception. Vision Research 2004, 44(22):2551-2557.
14. de Monasterio F.M. Properties of concentrically organized X and Y ganglion cells of macaque retina. Journal of Neurophysiology 1978, 41(6):1394-1417.
15. Di Russo F., Martinez A., Sereno M.I., Pitzalis S., Hillyard S.A. Cortical sources of the early components of the visual evoked potential. Human Brain Mapping 2002, 15(2):95-111.
16. Doniger G.M., Foxe J.J., Murray M.M., Higgins B.A., Javitt D.C. Impaired visual object recognition and dorsal/ventral stream interaction in schizophrenia. Archives of General Psychiatry 2002, 59(11):1011-1020.
17. Edwards V.T., Hogben J.H., Clark C.D., Pratt C. Effects of a red background on magnocellular functioning in average and specifically disabled readers. Vision Research 1996, 36:1037-1045.
18. Esterberg M.L., Compton M.T. The psychosis continuum and categorical versus dimensional diagnostic approaches. Current Psychiatry Reports 2009, 11(3):179-184.
19. Foxe J.J., Doniger G.M., Javitt D.C. Early visual processing deficits in schizophrenia: impaired P1 generation revealed by high-density electrical mapping. Neuroreport 2001, 12(17):3815-3820.
20. Foxe J.J., Murray M.M., Javitt D.C. Filling-in in schizophrenia: a high-density electrical mapping and source-analysis investigation of illusory contour processing. Cerebral Cortex 2005, 15(12):1914-1927.
21. Green M.F., Butler P.D., Chen Y., Geyer M.A., Silverstein S., Wynn J.K., et al. Perception measurement in clinical trials of schizophrenia: promising paradigms from CNTRICS. Schizophrenia Bulletin 2009, 35(1):163-181.
22. Javitt D.C. When doors of perception close: bottom-up models of disrupted cognition in schizophrenia. Annual Review of Clinical Psychology 2009, 5:249-275.
23. Kaplan E., Shapley R.M. The primate retina contains two types of ganglion cells, with high and low contrast sensitivity. Proceedings of the National Academy of Sciences USA 1986, 83(8):2755-2757.
24. Kelly J., Murray R.M. What risk factors tell us about the causes of schizophrenia and related psychoses. Current Psychiatry Reports 2000, 2(5):378-385.
25. Koychev I., El-Deredy W., Haenschel C., Deakin J.F.W. Visual information processing deficits as biomarkers of vulnerability to schizophrenia: an event-related potential study in schizotypy. Neuropsychologia 2010, 48(7):2205-2214.
26. Lalor E.C., De Sanctis P., Krakowski M.I., Foxe J.J. Visual sensory processing deficits in schizophrenia: Is there anything to the magnocellular account?. Schizophrenia Research 2012, 139(1-3):246-252.
27. Lalor E.C., Yeap S., Reilly R.B., Pearlmutter B.A., Foxe J.J. Dissecting the cellular contributions to early visual sensory processing deficits in schizophrenia using the VESPA evoked response. Schizophrenia Research 2008, 98(1-3):256-264.
28. Livingstone M.S., Hubel D.H. Anatomy and physiology of a color system in the primate visual cortex. Journal of Neuroscience 1984, 4(1):309-356.
29. Livingstone M.S., Hubel D.H. Psychophysical evidence for separate channels for the perception of form, color, movement, and depth. Journal of Neuroscience 1987, 7(11):3416-3468.
30. Martinez A., Hillyard S.A., Bickel S., Dias E.C., Butler P.D., Javitt D.C. Consequences of magnocellular dysfunction on processing attended information in schizophrenia. Cerebral Cortex 2011, 22(6):1282-1293.
31. Mohr C., Bracha H.S., Brugger P. Magical ideation modulates spatial behavior. The Journal of Neuropsychiatry and Clinical Neurosciences 2003, 15(2):168-174.
32. Obayashi C., Nakashima T., Onitsuka T., Maekawa T., Hirano Y., Hirano S., et al. Decreased spatial frequency sensitivities for processing faces in male patients with chronic schizophrenia. Clinical Neurophysiology 2009, 120(8):1525-1533.
33. Raine A. The schizotypal personality questionnaire (SPQ): a scale for the assessment of schizotypal personality based on DSM-III-R criteria. Schizophrenia Bulletin 1991, 17:555-564.
34. Schechter I., Butler P.D., Zemon V.M., Revheim N., Saperstein A.M., Jalbrzikowski M., et al. Impairments in generation of early-stage transient visual evoked potentials to magno- and parvocellular-selective stimuli in schizophrenia. Clinical Neurophysiology 2005, 116(9):2204-2215.
35. Vanni S., Warnking J., Dojat M., Delon-Martin C., Bullier J., Segebarth C. Sequence of pattern onset responses in the human visual areas: an fMRI constrained VEP source analysis. Neuroimage 2004, 21(3):801-817.
36. West G.L., Anderson A.A.K., Bedwell J.S., Pratt J. Red diffuse light suppresses the accelerated perception of fear. Psychological Science 2010, 21(7):992-999.
37. Wiesel T.N., Hubel D.H. Spatial and chromatic interactions in the lateral geniculate nucleus body of the rhesus monkey. Journal of Neurophysiology 1966, 29:1115-1156.
38. Yeap S., Kelly S.P., Reilly R.B., Thakore J.H., Foxe J.J. Visual sensory processing deficits in patients with bipolar disorder revealed through high-density electrical mapping. Journal of Psychiatry and Neuroscience 2009, 34(6):459-464.
39. Yeap S., Kelly S.P., Sehatpour P., Magno E., Garavan H., Thakore J.H., et al. Visual sensory processing deficits in Schizophrenia and their relationship to disease state. European Archives of Psychiatry and Clinical Neuroscience 2008, 258(5):305-316.
40. Yeap S., Kelly S.P., Sehatpour P., Magno E., Javitt D.C., Garavan H., et al. Early visual sensory deficits as endophenotypes for schizophrenia - high-density electrical mapping in clinically unaffected first-degree relatives. Archives of General Psychiatry 2006, 63(11):1180-1188.
41. Yeap S., Kelly S.P., Thakore J.H., Foxe J.J. Visual sensory processing deficits in first-episode patients with schizophrenia. Schizophrenia Research 2008, 102(1-3):340-343.