Electrophysiological evidence of corollary discharge dysfunction in schizophrenia during talking and thinking

Journal of Psychiatric Research

Volumn 38, Issue 1, 2004, Pages 37-46

  Ford, Judith M ^a,b   Mathalon, Daniel H ^c,d  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VA PALO ALTO HEALTH CARE SYSTEM   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d Vet Aff Connecticut Hlth Care S   (United States)

Author keywords

Corollary discharge; EEG coherence; N1; Schizophrenia

Indexed keywords

ADULT; AUDITORY CORTEX; AUDITORY HALLUCINATION; BRAIN NERVE CELL; CELL ACTIVITY; CONFERENCE PAPER; CONTROLLED STUDY; ELECTROENCEPHALOGRAM; ELECTROPHYSIOLOGY; ELECTRORETINOGRAM; EVENT RELATED POTENTIAL; FEMALE; FRONTAL CORTEX; HUMAN; MALE; NERVE CELL MEMBRANE POTENTIAL; PRIORITY JOURNAL; SCHIZOPHRENIA; SPEECH ARTICULATION; STIMULUS RESPONSE; TEMPORAL CORTEX; THINKING;

EID: 0346881159     PISSN: 00223956     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3956(03)00095-5     Document Type: Conference Paper

References (37)

1. Andreasen N.C. Scale for the assessment of positive symptoms. 1984;University of Iowa, Iowa City, IA.
2. Blakemore S., Rees G., Frith C. How do we predict the consequences of our actions? A functional imaging study. Neuropsychologia. 36:1998;521-529.
3. Creutzfeldt O., Ojeman G., Lettich E. Neuronal activity in the human lateral temporal lobe. I Responses to speech. Experimental Brain Research. 77:1989;451-475.
4. Creutzfeldt O., Ojeman G., Lettich E. Neuronal activity in the human lateral temporal lobe. II Responses to the subject's own voice. Experimental Brain Research. 77:1989;476-489.
5. Curio G., Neuloh G., Numminen J., Jousmaki V., Hari R. Speaking modifies voice-evoked activity in the human auditory cortex. Human Brain Mapping. 9:2000;183-191.
6. Davis H., Zerlin S. Acoustic relations of the human vertex potential. Journal of the Acoustic Society of America. 39:1966;109-116.
7. Dierks T., Linden D., Jandl M., Formisano E., Goebel R., Lanfermann H., Singer W. Activation of Heschl's Gyrus during auditory hallucinations. Neuron. 22:1999;615-621.
8. Feinberg I. Efference copy and corollary discharge: implications for thinking and its disorders. Schizophrenia Bulletin. 4:1978;636-640.
9. Feinberg I., Guazzelli M. Schizophrenia - a disorder of the corollary discharge systems that integrate the motor systems of thought with the sensory systems of consciousness. British Journal of Psychiatry. 174:1999;196-204.
10. First M.B., Spitzer R.L., Gibbon M., Williams J.B.W. Structured clinical interview for DSM-IV axis I disorders. 1995;Biometrics Research Department, New York State Psychiatric Institute, New York, NY.
11. Fletcher P., McKenna P.J., Friston K.J., Frith C.D., Dolan R.J. Abnormal cingulate modulation of fronto-temporal connectivity in schizophrenia. Neuroimage. 9:1999;337-342.
12. Ford J.M., Mathalon D.H., Heinks T., Kalba S., Roth W.T. Neurophysiological evidence of corollary discharge dysfunction in schizophrenia. American Journal of Psychiatry. 158:2001;2069-2071.
13. Ford J.M., Mathalon D.H., Kalba S., Whitfield S., Faustman W.O., Roth W.T. Cortical responsiveness during inner speech in schizophrenia: an event-related brain potential study. American Journal of Psychiatry. 158:2001;1914-1916.
14. Ford J.M., Mathalon D.H., Kalba S., Whitfield S., Faustman W.O., Roth W.T. Cortical responsiveness during talking and listening in schizophrenia: an event-related brain potential study. Biological Psychiatry. 50:2001;540-549.
15. Ford J.M., Mathalon D.H., Whitfield S., Faustman W.O., Roth W.T. Reduced communication between frontal and temporal lobes during talking in schizophrenia. Biological Psychiatry. 21:2002;485-492.
16. Friston K.J., Frith C.D. Schizophrenia: a disconnection syndrome? Clinical Neurosciences. 3:1995;89-97.
17. Fristonm K.J., Holmes A., Poline J-B., Price C.J., Frith C.D. Detecting activations in PET and fMRI: Levels of inference and power. Neuroimage. 4:1995;223-236.
18. Frith C.D., Done D.J. Experiences of alien control in schizophrenia reflect a disorder in the central monitoring of action. Psychological Medicine. 19:1989;359-363.
19. Frith C.D., Friston K., Liddle P.F., Frackowiak R.S.J. Willed action and the prefrontal cortex in man - a study with PET. Proceedings of the Royal Society of London Series B - Biological Sciences. 244:1991;241-246.
20. Han S., Liu W., Yund E., Woods D. Interactions between spatial attention and global/local feature selection: an ERP study. Neuroreport. 11:2000;2753-2758.
21. Hedlund J.L., Vieweg B.W. The Brief Psychiatric Rating Scale (BPRS): a comprehensive review. Journal of Operational Psychiatry. 11:1980;48-64.
22. Hillyard S.A., Hink R.F., Schwent V.L., Picton T.W. Electrical signs of selective attention in the human brain. Science. 182:1973;177-180.
23. Jackson J.H. Selected writings of John Hughlings Jackson. Taylor J. 1958;Basic Books, New York.
24. Lachaux J., Rodriguez E., Martinerie J., Varela F. Measuring phase synchrony in brain signals. Human Brain Mapping. 8:1999;194-208.
25. Manganotti P., Gerloff C., Toro C., Katsuta H., Sadato N., Zhuang P., Leocani L., Hallett M. Task-related coherence and task-related spectral power changes during sequential finger movements. Electroencephalography and clinical Neurophysiology. 109:1998;50-62.
26. Martinez A., Anllo-Vento L., Sereno M., Frank L., Buxton R., Dubowitz D., Wong E., Hinrichs H., Heinze H., Hillyard S. Involvement of striate and extrastriate visual cortical areas in spatial attention. Nature Neuroscience. 2:1999;364-369.
27. Muller-Preuss P., Ploog D. Inhibition of auditory cortical neurons during phonation. Brain Research. 215:1981;61-76.
28. Edit 4.1 Offline Analysis of Acquired Data: Coherence. SCAN™ User Guide Volume II. 1999;Neurosoft, Inc, Sterling, VA.
29. Norman R.M.G., Malla A.K., Williamson P.C., Morrison-Stewart S.L., Helmes E., Cortese L. EEG coherence and syndromes in schizophrenia. British Journal of Psychiatry. 170:1997;411-415.
30. Numminen J., Salmelin R., Hari R. Subject's own speach reduces reactivity of the human auditory cortex. Neuroscience Letters. 265:1999;119-122.
31. Overall J.E., Hollister L., Pichot R. Major psychiatric disorders. A four-dimensional model. Archives of General Psychiatry. 16:1967;146-151.
32. Papanicolaou A., Wilson G., Busch C., DeRego P., Orr C., Davis I., Eisenberg H. Hemispheric asymmetries in phonological processing assessed with probe evoked magnetic fields. International Journal of Neurosciences. 39:1988;275-281.
33. Paus T., Perry D.W., Zatorre R.J., Worsley K.J., Evans A.C. Modulation of cerebral blood flow in the human auditory cortex during speech: role of motor-to-sensory discharges. European Journal of Neuroscience. 8:1996;2236-2246.
34. Shergill S., Brammer M., Williams S., Murray R., McGuire P. Mapping auditory hallucinations in schizophrenia using functional magnetic resonance imaging. Archives of General Psychiatry. 57:2000;1033-1038.
35. Sperry R.W. Neural basis of the spontaneous optokinetic response produced by visual inversion. Journal of Comparative and Physiological Psychology. 43:1950;482-489.
36. Von Holst E., Mittelstaedt H. Das reafferenzprinzip. Naturwisshenschaften. 37:1950;464-476.
37. Warburton E., Wise R.J.S., Price C.J., Weiller C., Hadar U., Ramsay S., Frackowiak R.S.J. Noun and verb retrieval by normal subjects. studies with PET. Brain. 119:1996;159-179.