Magnocellular contributions to impaired motion processing in schizophrenia
Open accessAbstract
Patients with schizophrenia show impairments in motion processing, along with deficits in lower level processing primarily involving the magnocellular visual pathway. The present study investigates potential magnocellular contributions to impaired motion processing in schizophrenia using a combined neurophysiological and behavioral approach. As compared to prior motion studies in schizophrenia, thresholds were determined for both incoherent and coherent visual motion. In this study, velocity discrimination thresholds were measured for schizophrenia patients (n=14) and age-matched normal control subjects (n=16) using a staircase procedure. Early visual processing was evaluated using steady-state visual evoked potentials (ssVEP), with stimuli biased toward activation of either the magnocellular or parvocellular visual pathways through luminance contrast manipulation. Patients with schizophrenia showed poor velocity discrimination for both incoherent and coherent motion, with no significant group x task interaction. Further, when coherent motion performance was measured at individually determined incoherent motion thresholds, accuracy levels for patients were similar to controls, also indicating similarity of deficit for incoherent vs. coherent motion discrimination. Impairments in velocity discrimination correlated significantly with reduced amplitude of ssVEP elicited by magnocellular -- but not parvocellular -- selective stimuli. This study demonstrates that deficits in motion processing in schizophrenia are significantly related to reduced activation of the magnocellular visual system. Further, this study supports and extends prior reports of impaired motion processing in schizophrenia, and indicates significant bottom-up contributions to higher-order cognitive impairments.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Significant correlations between impaired motion perception and M-pathway dysfunction point to motion processing deficits in schizophrenia resulting from impaired gain control.
“Significant correlations between impaired motion perception and M-pathway dysfunction also point to motion processing deficits in schizophrenia resulting from impaired gain control (28).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [28]
Patients with schizophrenia show preferential M-pathway dysfunction, although deficits have also been observed in parvocellular processing.
“Patients with schizophrenia show preferential M-pathway dysfunction (21,22,28,35–38), although deficits have also been observed in parvocellular processing (19,20).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [28]
A large number of studies have reported motion processing deficits in schizophrenia.
“A large number of studies have reported motion processing deficits in schizophrenia (28–32).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [28]
Gain control deficits are related to higher-level problems in perceptual organization.
“There is also evidence that gain control deficits, seen in contrast detection and M-pathway deficits, are important in predicting outcome (22,45), and are related to higher-level problems in perceptual organization (28,46) and to symptomatology (20,47–51).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [28]
Numerous studies have shown motion processing deficits in schizophrenia.
“As discussed in the preceding text, numerous studies have shown motion processing deficits in schizophrenia (28,30–32,81).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [28]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783 · see citing works
Preface: Cerebral Cortex Has Come of Age
Goldman, P. S., & RAKIC, P. T. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1-a · Cited by 3,412 · see citing works
Social Class and Mental Illness
Hunt, R. G., Hollingshead, A. B., & Redlich, F. C. (1959) · The American Journal of Psychology · doi:10.2307/1420236 · Cited by 3,307 · see citing works
Recent advances in the phencyclidine model of schizophrenia
(1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.10.1301 · Cited by 2,904 · see citing works
Social Class and Mental Illness: A Community Study
Hollingshead, A. B., & Redlich, F. C. (2007) · American Journal of Public Health · doi:10.2105/ajph.97.10.1756 · Cited by 1,845 · see citing works
Zeki, S. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010452 · Cited by 982 · see citing works
A direct quantitative relationship between the functional properties of human and macaque V5
Rees, G. E., Friston, K. J., & Koch, C. (2000) · Nature Neuroscience · doi:10.1038/76673 · Cited by 650 · see citing works
Comparative mapping of higher visual areas in monkeys and humans
Orban, G. A., Van Essen, D., & Vanduffel, W. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.05.009 · Cited by 639 · see citing works
Ketamine-Induced NMDA Receptor Hypofunction as a Model of Memory Impairment and Psychosis
Newcomer, J. W. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(98)00067-0 · Cited by 604 · see citing works
The Glutamatergic Dysfunction Hypothesis for Schizophrenia
Coyle, J. T. (1996) · Harvard Review of Psychiatry · doi:10.3109/10673229609017192 · Cited by 568 · see citing works
Early-stage visual processing and cortical amplification deficits in schizophrenia
Butler, P. D., Zemon, V., Schechter, I., Saperstein, A. M., Hoptman, M. J., Lim, K. O., Revheim, N., Silipo, G., & Javitt, D. C. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.5.495 · Cited by 362 · see citing works
Self-citationDysfunction of Early-Stage Visual Processing in Schizophrenia
Butler, P. D., Schechter, I., Zemon, V. M., Schwartz, S. G., Greenstein, V. C., Gordon, J., Schroeder, C. E., & Javitt, D. C. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.7.1126 · Cited by 360 · see citing works
Self-citationMotion perception in schizophrenia
Chen, Y., Palafox, G. P., Nakayama, K., Levy, D. L., Matthysse, S., & Holzman, P. S. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.2.149 · Cited by 225 · see citing works
The NMDA Antagonist Model for Schizophrenia: Promise and Pitfalls
Abi-Saab, W., D'Souza, D., Moghaddam, B., & Krystal, J. (1998) · Pharmacopsychiatry · doi:10.1055/s-2007-979354 · Cited by 208 · see citing works
Foxe, J. J., Doniger, G. M., & Javitt, D. C. (2001) · Neuroreport · doi:10.1097/00001756-200112040-00043 · Cited by 185 · see citing works
Self-citationProcessing of global, but not local, motion direction is deficient in schizophrenia
Chen, Y. (2003) · Schizophrenia Research · doi:10.1016/s0920-9964(02)00222-0 · Cited by 183 · see citing works
McKeefry, D. J., Watson, J. D. G., Frackowiak, R. S. J., et al. (1997) · NeuroImage · doi:10.1006/nimg.1996.0246 · Cited by 173 · see citing works
Slaghuis, W. A. (1998) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.107.1.49 · Cited by 168 · see citing works
Slaghuis, W. A. (1998) · Journal of Abnormal Psychology · doi:10.1037//0021-843x.107.1.49 · Cited by 168 · see citing works
Selective deficits in visual perception and recognition in schizophrenia
O’Donnell, B. F., Swearer, J. M., Smith, L. T., Nestor, P. G., Shenton, M. E., & McCarley, R. W. (1996) · American Journal of Psychiatry · doi:10.1176/ajp.153.5.687 · Cited by 154 · see citing works
Coherent global motion in the absence of coherent velocity signals
Ross, J., Badcock, D. R., & Hayes, A. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00524-8 · Cited by 141 · see citing works
Sensory Information Processing in Neuroleptic-Naive First-Episode Schizophrenic Patients
Braus, D. F., Weber‐Fahr, W., Tost, H., Ruf, M., & Henn, F. A. (2002) · Archives of General Psychiatry · doi:10.1001/archpsyc.59.8.696 · Cited by 140 · see citing works
Butler, P. D., DeSanti, L. A., Maddox, J., Harkavy‐Friedman, J., AMADOR, X. F., Goetz, R. R., Javitt, D. C., & Gorman, J. M. (2002) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00341-3 · Cited by 139 · see citing works
Self-citationMagnocellular and parvocellular contributions to backward masking dysfunction in schizophrenia
Schechter, I., Butler, P. D., Silipo, G. S., Zemon, V. M., & Javitt, D. C. (2003) · Schizophrenia Research · doi:10.1016/s0920-9964(03)00008-2 · Cited by 134 · see citing works
Self-citationHeggelund, P., & Hartveit, E. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.6.1347 · Cited by 109 · see citing works
Functionally distinct groups of X‐cells in the lateral geniculate nucleus of the cat
Humphrey, A. L., & Weller, R. E. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902680311 · Cited by 103 · see citing works
The Multiple Roles of Visual Cortical Areas MT/MST in Remembering the Direction of Visual Motion
Bisley, J. W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.11.1053 · Cited by 95 · see citing works
Chen, Y., Bidwell, L. C., & Holzman, P. S. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.04.002 · Cited by 87 · see citing works
Vernier threshold in patients with schizophrenia and in their unaffected siblings
Kéri, S., Kelemen, O., Benedek, G., & Janka, Z. (2004) · Neuropsychology · doi:10.1037/0894-4105.18.3.537 · Cited by 84 · see citing works
Dysfunction of early-stage visual processing in schizophrenia: Harmonic analysis
Kim, D., Zemon, V., Saperstein, A., Butler, P. D., & Javitt, D. C. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2004.10.011 · Cited by 79 · see citing works
Self-citationKwon, Y. H., Esguerra, M., & Sur, M. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.2.414 · Cited by 79 · see citing works
Effect of stimulus contrast and size on NMDA receptor activity in cat lateral geniculate nucleus
Kwon, Y. H., Nelson, S. B., Toth, L. J., & Sur, M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.1.182 · Cited by 77 · see citing works
The effect of disrupting the human magnocellular pathway on global motion perception
Chapman, C. S., HOAG, R. A., & Giaschi, D. E. (2004) · Vision Research · doi:10.1016/j.visres.2004.06.003 · Cited by 72 · see citing works
Spatio-temporal luminance contrast sensitivity and visual backward masking in schizophrenia
Slaghuis, W. L. (2004) · Experimental Brain Research · doi:10.1007/s00221-003-1771-3 · Cited by 71 · see citing works
Compromised late-stage motion processing in schizophrenia
Chen, Y., Levy, D. L., Sheremata, S., & Holzman, P. S. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.12.024 · Cited by 70 · see citing works
Previc, F. H., Mario Liotti, A., Blakemore, C. B., Beer, J., & Fox, P. T. (2000) · Experimental Brain Research · doi:10.1007/s002219900298 · Cited by 65 · see citing works
Impaired detection of visual motion in schizophrenia patients
Li, C.-S. R. (2002) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(02)00207-5 · Cited by 60 · see citing works
Rivadulla, C., Sharma, J., & Sur, M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01710.2001 · Cited by 55 · see citing works
Neural Correlates of Chromatic Motion Perception
Thiele, A., Dobkins, K. R., & Albright, T. D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00463-9 · Cited by 54 · see citing works
Schwartz, B. D., Maron, B. A., Evans, W. J., & Winstead, D. K. (1999) · PubMed · Cited by 52 · see citing works
Magnetic response of human extrastriate cortex in the detection of coherent and incoherent motion
Lam, K., Kaneoke, Y., Gunji, A., Yamasaki, H. R., Matsumoto, E., Naito, T., & Kakigi, R. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00037-3 · Cited by 49 · see citing works
Psychometrically matched visual-processing tasks in schizophrenia spectrum disorders
Brenner, C. A., Wilt, M. A., Lysaker, P. H., Koyfman, A., & O'Donnell, B. F. (2003) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.112.1.28 · Cited by 46 · see citing works
Ulbert, I., Karmos, G., Heit, G., & Halgren, E. (2001) · Human Brain Mapping · doi:10.1002/hbm.1035 · Cited by 44 · see citing works
Humphrey, A. L., SAUL, A. B., & Feidler, J. C. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.6.3005 · Cited by 25 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Steady-state visually evoked potentials: Focus on essential paradigms and future perspectives
Vialatte, F.-B., Maurice, M., Dauwels, J., & Cichocki, A. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.11.005 · Cited by 1,066 · see citing works
When Doors of Perception Close: Bottom-up Models of Disrupted Cognition in Schizophrenia
Javitt, D. C. (2009) · Annual Review of Clinical Psychology · doi:10.1146/annurev.clinpsy.032408.153502 · Cited by 503 · see citing works
Self-citationVisual perception and its impairment in schizophrenia
Butler, P. D., Silverstein, S. M., & Dakin, S. C. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.03.023 · Cited by 472 · see citing works
Self-citationBussey, T. J., Holmes, A., Lyon, L., Mar, A. C., McAllister, K. A. L., Nithianantharajah, J., Oomen, C. A., & Saksida, L. M. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.011 · Cited by 299 · see citing works
Subcortical visual dysfunction in schizophrenia drives secondary cortical impairments
Butler, P. D., Martinez, A., Foxe, J. J., Kim, D., Zemon, V., Silipo, G., Mahoney, J., Shpaner, M., Jalbrzikowski, M., & Javitt, D. C. (2007) · Brain · doi:10.1093/brain/awl233 · Cited by 292 · see citing works
Self-citationWeakened center-surround interactions in visual motion processing in schizophrenia
Tadin, D., Kim, J., Doop, M. L., Gibson, C., Lappin, J. S., Blake, R., & Park, S. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2592-06.2006 · Cited by 182 · see citing works
Perception Measurement in Clinical Trials of Schizophrenia: Promising Paradigms From CNTRICS
Green, M. F., Butler, P. D., Chen, Y., Geyer, M. A., Silverstein, S., Wynn, J. K., Yoon, J. H., & Zemon, V. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn156 · Cited by 113 · see citing works
Self-citationConsequences of Magnocellular Dysfunction on Processing Attended Information in Schizophrenia
Martinez, A., Hillyard, S. A., Bickel, S., Dias, E. C., Butler, P. D., & Javitt, D. C. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr195 · Cited by 94 · see citing works
Self-citationAltered center-surround motion inhibition in schizophrenia
Chen, Y., Norton, D., & Ongur, D. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.11.017 · Cited by 51 · see citing works
Impaired magnocellular/dorsal stream activation predicts impaired reading ability in schizophrenia
Martínez, A., Revheim, N., Butler, P. D., Guilfoyle, D. N., Dias, E. C., & Javitt, D. C. (2013) · NeuroImage: Clinical · doi:10.1016/j.nicl.2012.09.006 · Cited by 45 · see citing works
Self-citationSlaghuis, W. L., Holthouse, T., Hawkes, A., & Bruno, R. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-1003-3 · Cited by 28 · see citing works
Altered ‘three-flash’ illusion in response to two light pulses in schizophrenia
Norton, D., Ongur, D., Stromeyer, C., & Chen, Y. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.03.002 · Cited by 18 · see citing works
A neural mechanism underlying predictive visual motion processing in patients with schizophrenia
Scheliga, S., Schwank, R., Scholle, R., Habel, U., & Kellermann, T. (2022) · Psychiatry Research · doi:10.1016/j.psychres.2022.114934 · Cited by 8 · see citing works
- Authors
- Kim, D., Wylie, G., Pasternak, R., Butler, P. D., & Javitt, D. C.
- Affiliations
- Nathan Kline Institute for Psychiatric Research (US)
- Corresponding author
- Javitt, Daniel C.
- Venue
- Schizophrenia Research
- Publisher
- Elsevier BV
- Published
- 2006-02
- Volume
- 82
- Issue
- 1
- Pages
- 1-8
- ISSN
- 0920-9964 (ISSN-L)
- PMC
- PMC2045640
- OpenAlex
- W2128944881
- Cited by
- 146
- References
- 44
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 5 · 2023: 3 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 9 · 2018: 8 · 2017: 4 · 2016: 7 · 2015: 7 · 2014: 4 · 2013: 10 · 2012: 9
- FWCI
- 5.01
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Schizophrenia Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Wellcome Trust
- National Institute of Mental Health (R37MH049334, R01MH066374, K02-MH-01439, R01 MH49334, R01MH049334, K02MH001439)
- 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 › Hallucinations in medical conditions
- Keywords
- schizophrenia, motion processing
- MeSH terms
- Adult, Evoked Potentials, Visual, Female, Humans, Male, Motion Perception, Perceptual Disorders, Schizophrenia, Visual Fields, Visual Pathways, Visual Perception, Vision, Binocular, Diagnostic and Statistical Manual of Mental Disorders
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