Failure to use corollary discharge to remap visual target locations is associated with psychotic symptom severity in schizophrenia
Open accessAbstract
Corollary discharge (CD) refers to "copies" of motor signals sent to sensory areas, allowing prediction of future sensory states. They enable the putative mechanisms supporting the distinction between self-generated and externally generated sensations. Accordingly, many authors have suggested that disturbed CD engenders psychotic symptoms of schizophrenia, which are characterized by agency distortions. CD also supports perceived visual stability across saccadic eye movements and is used to predict the postsaccadic retinal coordinates of visual stimuli, a process called remapping. We tested whether schizophrenia patients (SZP) show remapping disturbances as evidenced by systematic transsaccadic mislocalizations of visual targets. SZP and healthy controls (HC) performed a task in which a saccadic target disappeared upon saccade initiation and, after a brief delay, reappeared at a horizontally displaced position. HC judged the direction of this displacement accurately, despite spatial errors in saccade landing site, indicating that their comparison of the actual to predicted postsaccadic target location relied on accurate CD. SZP performed worse and relied more on saccade landing site as a proxy for the presaccadic target, consistent with disturbed CD. This remapping failure was strongest in patients with more severe psychotic symptoms, consistent with the theoretical link between disturbed CD and phenomenological experiences in schizophrenia.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The symptomatology of schizophrenia-such as thought insertion-has been understood in terms of a failure of sensory attenuation mechanisms.
“For instance, the symptomatology of schizophrenia—such as thought insertion, where patients report feeling that their thoughts are not their own—have been understood in terms of a failure of these sensory attenuation mechanisms (Ford and Mathalon 2005; Frith 2005; Rösler et al. 2015; Thakkar et al. 2021).”
From Consciousness in active inference: Deep self-models, other minds, and the challenge of psychedelic-induced ego-dissolution (2021) · cites this paper as Rösler et al. 2015
Cites
The Positive and Negative Syndrome Scale (PANSS) for schizophrenia.
Kay, S. R., Fiszbein, A., & Opler, L. A. (1987) · Schizophrenia Bulletin · doi:10.1093/schbul/13.2.261 · Cited by 21,378 · see citing works
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 19,308 · see citing works
(1966) · Medical Entomology and Zoology · Cited by 10,293 · see citing works
Signal detection theory and psychophysics
Ingleby, D. (1967) · Journal of Sound and Vibration · doi:10.1016/0022-460x(67)90197-6 · Cited by 8,616 · see citing works
SCAN: Schedules fonr Clinical Assessment in Neuropsychiatry
Wing, J. K. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810180089012 · Cited by 2,517 · see citing works
Chlorpromazine Equivalent Doses for the Newer Atypical Antipsychotics
Woods, S. W. (2003) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v64n0607 · Cited by 2,056 · see citing works
The cognitive neuropsychology of schizophrenia
(1993) · Choice Reviews Online · doi:10.5860/choice.31-0601 · Cited by 1,901 · see citing works
The Comprehensive Assessment of Symptoms and History (CASH)
Andreasen, N. C. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820080023004 · Cited by 1,314 · see citing works
Leucht, S., Kane, J., Kissling, W., Hamann, J., Etschel, E., & Engel, R. R. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.04.008 · Cited by 1,230 · see citing works
The Eyelink Toolbox: Eye tracking with MATLAB and the Psychophysics Toolbox
Cornelissen, F. W., Peters, E. M., & Palmer, J. C. (2002) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03195489 · Cited by 1,049 · see citing works
Corollary discharge across the animal kingdom
Crapse, T. B., & Sommer, M. A. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2457 · Cited by 789 · see citing works
Working Memory Impairments in Schizophrenia: A Meta-Analysis.
Lee, J., & Park, S. (2005) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.114.4.599 · Cited by 770 · see citing works
Efference copy and corollary discharge: implications for thinking and its disorders
Feinberg, I. (1978) · Schizophrenia Bulletin · doi:10.1093/schbul/4.4.636 · Cited by 592 · see citing works
Neuronal mechanisms of visual stability
Wurtz, R. H. (2008) · Vision Research · doi:10.1016/j.visres.2008.03.021 · Cited by 587 · see citing works
A Pathway in Primate Brain for Internal Monitoring of Movements
Sommer, M. A., & Wurtz, R. H. (2002) · Science · doi:10.1126/science.1069590 · Cited by 565 · see citing works
Thalamocortical Dysconnectivity in Schizophrenia
Woodward, N. D., Karbasforoushan, H., & Heckers, S. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12010056 · Cited by 514 · see citing works
Brain Circuits for the Internal Monitoring of Movements
Sommer, M. A., & Wurtz, R. H. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125627 · Cited by 508 · see citing works
The cognitive neuropsychology of schizophrenia
Cutting, J. (1993) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(93)90160-h · Cited by 451 · see citing works
Comparing correlated but nonoverlapping correlations.
Raghunathan, T. E., Rosenthal, R., & Rubin, D. B. (1996) · Psychological Methods · doi:10.1037/1082-989x.1.2.178 · Cited by 262 · see citing works
Sommer, M. A., & Wurtz, R. H. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00740.2003 · Cited by 254 · see citing works
Lindner, A., Thier, P., Kircher, T. T. J., Haarmeier, T., & Leube, D. (2005) · Current Biology · doi:10.1016/j.cub.2005.05.049 · Cited by 198 · see citing works
Visual space is compressed in prefrontal cortex before eye movements
Zirnsak, M., Steinmetz, N. A., Noudoost, B., Xu, K. Z., & Moore, T. (2014) · Nature · doi:10.1038/nature13149 · Cited by 195 · see citing works
A Dynamical Systems Hypothesis of Schizophrenia
Loh, M., Rolls, E. T., & Deco, G. (2007) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030228 · Cited by 164 · see citing works
Shinn, A. K., Baker, J. T., Cohen, B. M., & Öngür, D. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.11.037 · Cited by 128 · see citing works
Post-saccadic location judgments reveal remapping of saccade targets to non-foveal locations
Collins, T., Rolfs, M., Deubel, H., et al. (2009) · Journal of Vision · doi:10.1167/9.5.29 · Cited by 127 · see citing works
Self-citationEvidence That Familial Liability for Psychosis Is Expressed as Differential Sensitivity to Cannabis
(2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.132 · Cited by 123 · see citing works
Anticevic, A., Yang, G. R., Savić, A., Murray, J. D., Cole, M. W., Repovš, G., Pearlson, G. D., & Glahn, D. C. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu100 · Cited by 111 · see citing works
Human thalamus contributes to perceptual stability across eye movements
Ostendorf, F., Liebermann, D., & Ploner, C. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910742107 · Cited by 92 · see citing works
Remapping for visual stability
Hall, N. J., & Colby, C. L. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0248 · Cited by 89 · see citing works
Disrupted Saccadic Corollary Discharge in Schizophrenia
Thakkar, K. N., Schall, J. D., Heckers, S., & Park, S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0473-15.2015 · Cited by 63 · see citing works
Self-citationEfference Copy Failure during Smooth Pursuit Eye Movements in Schizophrenia
Spering, M., Dias, E. C., Sanchez, J. L., Schütz, A. C., & Javitt, D. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0578-13.2013 · Cited by 57 · see citing works
Components of the smooth pursuit function in deficit and nondeficit schizophrenia
Hong, L. E., Avila, M. T., Adami, H. M., Elliott, A., & Thaker, G. K. (2003) · Schizophrenia Research · doi:10.1016/s0920-9964(02)00388-2 · Cited by 50 · see citing works
Does pursuit abnormality in schizophrenia represent a deficit in the predictive mechanism?
Thaker, G. K., Ross, D. E., Buchanan, R. W., et al. (1996) · Psychiatry Research · doi:10.1016/0165-1781(95)02759-9 · Cited by 41 · see citing works
Impaired Smooth Pursuit in Schizophrenia Results from Prediction Impairment Only
Nkam, I., Bocca, M., Denise, P., Paolettí, X., Dollfus, S., Levillain, D., & Thibaut, F. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.11.029 · Cited by 27 · see citing works
Response to unexpected target changes during sustained visual tracking in schizophrenic patients
Hong, L. E., Avila, M. T., & Thaker, G. K. (2005) · Experimental Brain Research · doi:10.1007/s00221-005-2276-z · Cited by 25 · see citing works
Corollary discharge contributes to perceived eye location in monkeys
Joiner, W. M., Cavanaugh, J. R., FitzGibbon, E. J., et al. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00362.2013 · Cited by 24 · see citing works
Perisaccadic Perception of Visual Space in People with Schizophrenia
Richard, A., Churan, J., Whitford, V., O’Driscoll, G. A., Titone, D. A., & Pack, C. C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4744-13.2014 · Cited by 21 · see citing works
Trajectory Integration of Shape and Color of Moving Object
Nishida, S., Terao, M., & Watanabe, J. (2010) · Journal of Vision · doi:10.1167/9.8.21 · Cited by 7 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Hallucinations and strong priors
Corlett, P. R., Horga, G., Fletcher, P. C., Alderson-Day, B., Schmack, K., & Powers, A. R. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.12.001 · Cited by 534 · see citing works
Oculomotor prediction: A window into the psychotic mind
Thakkar, K. N., Diwadkar, V. A., & Rolfs, M. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.02.001 · Cited by 66 · see citing works
Self-citationDeane, G. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab024 · Cited by 38 · see citing works
“For instance, the symptomatology of schizophrenia—such as thought insertion, where patients report feeling that their thoughts are not their own—have been understood in terms of a failure of these sensory attenuation mechanisms (Ford and Mathalon 2005; Frith 2005; Rösler et al. 2015; Thakkar et al. 2021).”
Background
- Authors
- Rösler, L., Rolfs, M., van der Stigchel, S., Neggers, S. F. W., Cahn, W., Kahn, R. S., & Thakkar, K. N.
- Affiliations
- Goethe University Frankfurt (DE)
- Humboldt-Universität zu Berlin (DE)
- Department of Experimental Psychology, Helmholtz Institute, Utrecht University, Utrecht, The Netherlands; and
- University Medical Center Utrecht (NL)
- Corresponding author
- Thakkar, Katharine N.
- ORCID
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 2015-08
- Volume
- 114
- Issue
- 2
- Pages
- 1129-1136
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- PMC
- PMC4541139
- OpenAlex
- W2176081155
- Cited by
- 34
- References
- 38
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 3 · 2023: 2 · 2021: 4 · 2020: 2 · 2019: 5 · 2018: 5 · 2017: 4 · 2016: 5 · 2015: 1
- FWCI
- 4.05
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Neurophysiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- Utrecht University Repository (Utrecht University) (submittedVersion)
- Funders
- Nederlands Organisation for Scientific Research (Rubicon grant)
- DFG Emmy Noether grant (RO 3579/2-1)
- Dutch Health Resesarch Council (ZON-MW 10-000-1001)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- corollary discharge, schizophrenia, psychotic symptoms, saccades, agency, visual stability
- MeSH terms
- Adult, Biomechanical Phenomena, Female, Humans, Judgment, Longitudinal Studies, Male, Neuropsychological Tests, Photic Stimulation, Psychiatric Status Rating Scales, Saccades, Schizophrenia, Schizophrenic Psychology, Space Perception, Antipsychotic Agents
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review