Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-20T05:42:50.475Z Has data issue: false hasContentIssue false

Clinical, cognitive and neural correlates of self-monitoring deficits in schizophrenia: an update

Published online by Cambridge University Press:  24 June 2014

Vinodkumar Raveendran*
Affiliation:
Departments of Psychology Neuroscience, Institute of Psychiatry, King’s College London, London, UK
Veena Kumari
Affiliation:
Departments of Psychology
*
Vinodkumar Raveendran, MB BS, MD, Department of Psychology, PO Box 78, Institute of Psychiatry, King’s College London, De Crespigny Park, London SE5 8AF, UK. Tel: 44 207 848 0978; Fax: 44 207 848 0646; E-mail: [email protected]

Abstract

Background:

An area of recent interest in schizophrenia research is to investigate specific neural and cognitive abnormalities associated with symptoms of this disorder.

Objective:

To establish clinical, cognitive and neural correlates of self-monitoring deficits in schizophrenia, which according to various theoretical models can account for the first-rank symptoms of this disorder.

Methods:

Relevant data were identified from PubMed and PsycInfo searches up to July 2006 using combinations of keywords including ‘self-monitoring’, ‘symptoms’, ‘self-agency’, ‘neuropsychological’, ‘cognitive’, ‘brain activity’, ‘PET’ and ‘fMRI’.

Conclusions:

Self-monitoring deficit is most consistently observed in patients with schizophrenia with auditory hallucinations and passivity experiences. This deficit may not be schizophrenia specific. At present, there are insufficient direct data to reach meaningful conclusions about the cognitive correlates of this deficit. Functional neuroimaging studies in patients with schizophrenia with auditory hallucinations point to defective engagement of the neural regions known to be involved in self-monitoring in healthy people. Further multimodal studies using validated cognitive and clinical measures, self-monitoring paradigms and appropriate imaging tools to analyze patients with schizophrenia with and without self-monitoring deficits are required to increase our understanding of this topic.

Type
Review article
Copyright
Copyright © 2007 Blackwell Munksgaard

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Jablensky, A. Epidemiology of schizophrenia: the global burden of disease and disability. Eur Arch Psychiatry Clin Neurosci 2000;250:274285. CrossRefGoogle ScholarPubMed
Murray, RM, Castle, DJ. Genetic and environmental risk factors for schizophrenia. In: Gelder, MG, Lopez-Ibor, J Jr, Andreasen, NC, eds. New Oxford textbook of psychiatry. Oxford, UK: Oxford University Press, 2000: 599605. Google Scholar
Frith, CD. The cognitive neuropsychology of schizophrenia. Erlbaum, UK: Taylor and Francis, 1992. Google ScholarPubMed
Schneider, K. Clinical psychopathology. 5th edn. New York: Grune and Stratton, 1959. Google Scholar
Farrer, C, Frith, CD. Experiencing oneself vs another person as being the cause of action: the neural correlates of the experience of agency. Neuroimage 2002;15:596603. CrossRefGoogle ScholarPubMed
Grezes, J, Frith, CD, Passingham, RE. Inferring false beliefs from the actions of oneself and others: an fMRI study. Neuroimage 2004;21:744750. CrossRefGoogle Scholar
Haggard, P, Clark, S. Intentional action: conscious experience and neural prediction. Conscious Cogn 2003;12:695707. CrossRefGoogle ScholarPubMed
Leube, DT, Knoblich, G, Erb, M, Kircher, TTJ. Observing one’s hand become anarchic: an fMRI study of action identification. Conscious Cogn 2003;12:597608. CrossRefGoogle ScholarPubMed
Kircher, T, David, AS. Self-consciousness: an integrative approach from philosophy, psychopathology and the neurosciences. In: Kircher, T, David, A, eds. The self in neuroscience and psychiatry. Cambridge, UK: Cambridge University Press, 2003: 445473. CrossRefGoogle Scholar
Kircher, TT, Leube, DT. Self-consciousness, self-agency, and schizophrenia. Conscious Cogn 2003;12:656669. CrossRefGoogle Scholar
Blakemore, SJ, Frith, C. Self-awareness and actions. Curr Opin Neurobiol 2003;13:219224. CrossRefGoogle Scholar
Wolpert, DM, Miall, RC. Forward models for physiological motor control. Neural Netw 1996;9:12651279. Google ScholarPubMed
Frith, C. The self in action: lessons from delusions of control. Conscious Cogn 2005;14:752770. CrossRefGoogle ScholarPubMed
Frith, CD, Blakemore, SJ, Wolport, DM. Explaining the symptoms of schizophrenia: abnormalities in the awareness of action. Brain Res Brain Res Rev 2000;31:357363. CrossRefGoogle ScholarPubMed
Frith, CD, Blakemore, SJ, Wolport, DM. Abnormalities in the awareness and control of action. Philos Trans R Soc Lond B Biol Sci 2000;355:17711788. CrossRefGoogle ScholarPubMed
Wolpert, DM, Ghahramani, Z, Jordan, MI. An internal model for sensorimotor integration. Science 1995;269:18801882. CrossRefGoogle ScholarPubMed
Blakemore, SJ. Deluding the motor system. Conscious Cogn 2003;12:647655. CrossRefGoogle ScholarPubMed
Libet, B, Gleason, CA, Wright, EW, Pearl, DK. Time of conscious intention to act in relation to onset of cerebral activity (readiness-potential). The unconscious initiation of a freely voluntary act. Brain 1983;106:623642. CrossRefGoogle ScholarPubMed
Jeannerod, M, Pacherie, E. Agency, simulation and self identification. Mind Lang 2004;19:113146. CrossRefGoogle Scholar
Georgieff, N, Jeannerod, M. Beyond consciousness of external reality: a “who” system for consciousness of action and self-consciousness. Conscious Cogn 1998;7:465477. CrossRefGoogle ScholarPubMed
Jeannerod, M, Farrer, C, Franck, Fet al. Action recognition in normal and schizophrenic subjects. In: Kircher, T, David, A, eds. The self in neuroscience and psychiatry. Cambridge, UK: Cambridge University Press, 2003: 380406. CrossRefGoogle Scholar
Pacherie, E, Green, M, Bayne, T. Phenomenology and delusions: who put the ‘alien’ in alien control? Conscious Cogn 2006;15:566577. CrossRefGoogle ScholarPubMed
Blackmore, SJ, Wolport, DM, Frith, CD. Central cancellation of self-produced tickle sensation. Nat Neurosci 1998;1:635640. CrossRefGoogle Scholar
Haggard, P, Clark, S, Kalogeras, J. Voluntary action and conscious awareness. Nat Neurosci 2002;5:382385. CrossRefGoogle ScholarPubMed
Pisella, L, Grea, H, Tilikete, Cet al. An ‘automatic pilot’ for the hand in human posterior parietal cortex: toward reinterpreting optic ataxia. Nat Neurosci 2000;3:729736. Google ScholarPubMed
Daprati, E, Franck, N, Georgieff, Net al. Looking for the agent: an investigation into consciousness of action and self-consciousness in schizophrenic patients. Cognition 1997;65:7186. CrossRefGoogle ScholarPubMed
Farrer, C, Franck, N, Georgieff, N, Frith, CD, Decety, J, Jeannerod, M. Modulating the experience of agency: a positron emission tomography study. Neuroimage 2003;18:324333. CrossRefGoogle ScholarPubMed
David, A. Diagnosis, classification and differential diagnosis of schizophrenia. In: Gelder, MG, Lopez-Ibor, J Jr, Andreasen, NC, eds. New Oxford textbook of psychiatry. Oxford, UK: Oxford University Press, 2000: 579584. Google Scholar
Blakemore, SJ, Wolport, DM, Frith, CD. Abnormalities in the awareness of action. Trends Cogn Sci 2002;6:237242. CrossRefGoogle ScholarPubMed
Jones, SR, Fernyhough, C. Thought as action: inner speech, self-monitoring and auditory verbal hallucinations. In press. doi:10.1016/jconcog.2005.12.003, Conscious Cogn 2006. Published Online 7 Feb 2006. Google ScholarPubMed
Spence, SA. Freewill in the light of neuropsychiatry. Philos Psychiatry Psychol 1996;3:7590. CrossRefGoogle Scholar
Gallagher, S. Neurocognitive models of schizophrenia: a neurophenomenological critique. Psychopathology 2004;37:819. CrossRefGoogle ScholarPubMed
Seal, ML, Aleman, A, McGuire, PK. Compelling imagery, unanticipated speech and deceptive memory: neurocognitive models of auditory verbal hallucinations in schizophrenia. Cognit Neuropsychiatry 2004;9:4372. CrossRefGoogle Scholar
Frith, CD, Done, DJ. Experiences of alien control in schizophrenia reflect a disorder in the central monitoring of action. Psychol Med 1989;19:359363. CrossRefGoogle Scholar
Malenka, RC, Angel, RW, Hampton, B, Berger, PA. Impaired central error-correcting behaviour in schizophrenia. Arch Gen Psychiatry 1982;39:101107. CrossRefGoogle Scholar
Mlakar, J, Jensterle, J, Frith, CD. Central monitoring deficiency and schizophrenic symptoms. Psychol Med 1994;24:557564. CrossRefGoogle ScholarPubMed
Stirling, JD, Hellewell, JS, Quraishi, N. Self-monitoring dysfunction and the schizophrenic symptoms of alien control. Psychol Med 1998;28:675683. CrossRefGoogle ScholarPubMed
Blakemore, SJ, Smith, J, Steel, R, Johnstone, CE, Frith, CD. The perception of self-produced sensory stimuli in patients with auditory hallucinations and passivity experiences: evidence for a breakdown in self-monitoring. Psychol Med 2000;30:11311139. CrossRefGoogle ScholarPubMed
Danckert, J, Rossetti, Y, D’Amato, T, Dalery, J, Saoud, M. Exploring imagined movements in patients with schizophrenia. Neuroreport 2002;13:605609. CrossRefGoogle ScholarPubMed
Maruff, P, Wilson, P, Currie, J. Abnormalities of motor imagery associated with somatic passivity phenomena in schizophrenia. Schizophr Res 2003;60:229238. CrossRefGoogle Scholar
Delevoye-Turrell, Y, Giersch, A, Danion, JM. Abnormal sequencing of motor actions in patients with schizophrenia: evidence from grip force adjustments during object manipulation. Am J Psychiatry 2003;160:134141. CrossRefGoogle ScholarPubMed
Delevoye-Turrell, Y, Giersch, A, Danion, JM. A deficit in the adjustment of grip force responses in schizophrenia. Neuroreport 2002;13:15371539. CrossRefGoogle Scholar
Knoblich, G, Stottmeister, F, Kircher, T. Self-monitoring in patients with schizophrenia. Psychol Med 2004;34:15611569. CrossRefGoogle ScholarPubMed
Cahill, C, Silbersweig, D, Frith, C. Psychotic experiences induced in deluded patients using distorted auditory feedback. Cognit Neuropsychiatry 1996;1:201211. CrossRefGoogle ScholarPubMed
Johns, LC, McGuire, PK. Verbal self-monitoring and auditory hallucinations in schizophrenia. Lancet 1999;353:469470. CrossRefGoogle Scholar
Johns, LC, Rossell, S, Frith, Cet al. Verbal self-monitoring and auditory verbal hallucinations in patients with schizophrenia. Psychol Med 2001;31:705715. CrossRefGoogle ScholarPubMed
Allen, PP, Johns, LC, Fu, CH, Broome, MR, Vythelingum, GN, McGuire, PK. Misattribution of external speech in patients with hallucinations and delusions. Schizophr Res 2004;69:277287. CrossRefGoogle ScholarPubMed
Fourneret, P, Jeannerod, M. Limited conscious monitoring of motor performance in normal subjects. Neuropsychologia 1998;36:11331140. CrossRefGoogle ScholarPubMed
Fourneret, P, Franck, N, Slachevsky, A, Jeannerod, M. Self-monitoring in schizophrenia revisited. Neuroreport 2001;12:12031208. CrossRefGoogle ScholarPubMed
De Vignemont, F, Fourneret, P. The sense of agency: a philosophical and empirical review of the “Who” system. Conscious Cogn 2004;13:119. CrossRefGoogle ScholarPubMed
Fourneret, P, De Vignemont, F, Franck, N, Slachevsky, A, Dubois, B, Jeannerod, M. Perception of self-generated action in schizophrenia. Cognit Neuropsychiatry 2002;7:139156. CrossRefGoogle Scholar
Rankin, PM, O’Carroll, PJ. Reality discrimination, reality monitoring and disposition towards hallucination. Br J Clin Psychol 1994;34:517528. CrossRefGoogle ScholarPubMed
Johns, LC, Gregg, L, Allen, P, McGuire, PK. Impaired verbal self-monitoring in psychosis: effects of state, trait and diagnosis. Psychol Med 2006;36:465474. CrossRefGoogle ScholarPubMed
Malenka, RC, Angel, RW, Thiemann, S, Weitz, CJ, Berger, PA. Central error-correcting behaviour in schizophrenia and depression. Biol Psychiatry 1986;21:263273. CrossRefGoogle ScholarPubMed
Lindner, A, Thier, P, Kircher, TT, Haarmeier, T, Leube, DT. Disorders of agency in schizophrenia correlate with an inability to compensate for the sensory consequences of actions. Curr Biol 2005;15:11191124. CrossRefGoogle ScholarPubMed
Stirling, JD, Hellewell, JS, Ndlovu, D. Self-monitoring dysfunction and the positive symptoms of schizophrenia. Psychopathology 2001;34:198202. CrossRefGoogle ScholarPubMed
Goldberg, TE, Gold, JM, Coppola, R, Weinberger, DR. Unnatural practices, unspeakable actions: a study of delayed auditory feedback in schizophrenia. Am J Psychiatry 1997;154:858860. Google Scholar
Turken, AU, Vuilleumier, P, Mathalon, DH, Swick, D, Ford, JM. Are impairments of action monitoring and executive control true dissociative dysfunctions in patients with schizophrenia? Am J Psychiatry 2003;160:18811883. CrossRefGoogle ScholarPubMed
Posada, A, Franck, N, Georgieff, N, Jeannerod, M. Anticipating incoming events: an impaired cognitive process in schizophrenia. Cognition 2001;81:209225. CrossRefGoogle Scholar
Creutzfeldt, O, Ojeman, G, Lettich, E. Neuronal activity in the human lateral temporal lobe. II. Responses to subjects’ own voice. Exp Brain Res 1989;77:476489. CrossRefGoogle Scholar
Fu, CH, Vythelingum, N, Brammer, MJet al. An fMRI study of verbal self-monitoring: neural correlates of auditory verbal feedback. Cereb Cortex 2006;16:969977. CrossRefGoogle ScholarPubMed
Friston, KJ, Frith, CD, Liddle, PF, Frackowiak, RS. Investigating a network model of word generation with positron emission tomography. Proc Biol Sci 1991;244:101106. CrossRefGoogle ScholarPubMed
McGuire, PK, Silbersweig, DA, Frith, CD. Functional neuroanatomy of verbal self-monitoring. Brain 1996;119:907917. CrossRefGoogle ScholarPubMed
Allen, PP, Amaro, E, Fu, CHet al. Neural correlates of the misattribution of self-generated speech. Hum Brain Mapp 2005;26:4453. CrossRefGoogle ScholarPubMed
McGuire, PK, Silbersweig, DA, Murray, RM, David, AS, Frackowiak, RS, Frith, CD. Functional anatomy of inner speech and auditory verbal imagery. Psychol Med 1996;26:2938. CrossRefGoogle ScholarPubMed
Shergill, SS, Bullmore, ET, Brammer, MJ, Williams, SC, Murray, RM, McGuire, PK. A functional study of auditory verbal imagery. Psychol Med 2001;31:241253. CrossRefGoogle ScholarPubMed
Blakemore, SJ, Wolpert, D, Frith, C. Why can’t you tickle yourself? Neuroreport 2000;11:R11R16. CrossRefGoogle ScholarPubMed
Blakemore, J, Frith, CD, Wolpert, D. The cerebellum is involved in predicting the sensory consequences of action. Neuroreport 2001;12:18791884. CrossRefGoogle Scholar
Leube, DT, Knoblich, G, Erb, M, Grodd, W, Bartel, M, Kircher, TTJ. The neural correlates of perceiving one’s own movements. Neuroimage 2003;20:20842090. CrossRefGoogle ScholarPubMed
Frith, C. The prefrontal cortex in self-consciousness. Philos Trans R Soc Lond B Biol Sci 1996;351:15051512. CrossRefGoogle ScholarPubMed
Kasai, K, Iwanami, A, Yamasue, H, Kuroki, N, Nakagome, K, Fukuda, M. Neuroanatomy and neurophysiology in schizophrenia. Neurosci Res 2002;43:93110. CrossRefGoogle Scholar
Shenton, ME, Dickey, CC, Frumin, M, McCarley, RW. A review of MRI findings in schizophrenia. Schizophr Res 2001;49:152. CrossRefGoogle Scholar
Hunter, MD, Griffiths, TD, Farrow, TFet al. A neural basis for the perception of voices in external auditory space. Brain 2003;126:161169. CrossRefGoogle ScholarPubMed
McGuire, PK, Shah, GM, Murray, RM. Increased blood flow in Broca’s area during auditory hallucinations in schizophrenia. Lancet 1993;342:703706. CrossRefGoogle Scholar
Shergill, SS, Bullmore, E, Simmons, A, Murray, R, McGuire, P. Mapping auditory hallucinations in schizophrenia using functional magnetic resonance imaging. Arch Gen Psychiatry 2000;59:468489. Google Scholar
Silbersweig, DA, Stern, E, Frith, Cet al. A functional neuroanatomy of hallucinations in schizophrenia. Nature 1995;378:176179. CrossRefGoogle Scholar
Sokhi, DS, Hunter, MD, Wilkinson, ID, Woodruff, PW. Male and female voices activate distinct regions in the male brain. Neuroimage 2005;27:572578. CrossRefGoogle ScholarPubMed
Frith, C. Neuropsychology of schizophrenia, what are the implications of intellectual and experiential abnormalities for the neurobiology of schizophrenia? Br Med Bull 1996;52:618626. CrossRefGoogle ScholarPubMed
Frith, CD, Friston, KJ, Herold, Set al. Regional brain activity in chronic schizophrenic patients during the performance of a verbal fluency task. Br J Psychiatry 1995;167:343349. CrossRefGoogle ScholarPubMed
Fu, CH, Vythelingum, GN, Andrew, Cet al. Alien voices … who said that? Neural correlates of impaired verbal self-monitoring in schizophrenia. Neuroimage 2001;13:S1052. CrossRefGoogle Scholar
McGuire, PK, Silbersweig, DA, Wright, Iet al. Abnormal monitoring of inner speech: a physiological basis for auditory hallucinations. Lancet 1995;346:596600. CrossRefGoogle ScholarPubMed
McGuire, PK, Silbersweig, DA, Wright, I, Murray, RM, Frackowiak, RS, Frith, CD. The neural correlates of inner speech and auditory verbal imagery in schizophrenia: relationship to auditory verbal hallucinations. Br J Psychiatry 1996;169:148159. CrossRefGoogle ScholarPubMed
Shergill, SS, Bullmore, E, Simmons, A, Murray, R, McGuire, P. Functional anatomy of auditory verbal imagery in schizophrenic patients with auditory hallucinations. Am J Psychiatry 2000;157:16911693. CrossRefGoogle ScholarPubMed
Shergill, SS, Brammer, MJ, Fukuda, R, Williams, SC, Murray, RM, McGuire, PK. Engagement of brain areas implicated in processing inner speech in people with auditory hallucinations. Br J Psychiatry 2003;182:525531. CrossRefGoogle ScholarPubMed
Gray, JA, Feldon, J, Rawlins, JNP, Hemsley, DR, Smith, AD. The neuropsychology of schizophrenia. Behav Brain Sci 1991;14:119. CrossRefGoogle Scholar
Frith, CD, Done, DJ. Towards a neuropsychology of schizophrenia. Br J Psychiatry 1988;153:437443. CrossRefGoogle ScholarPubMed
Ford, JM, Mathalon, DH, Heinks, T, Kalba, S, Faustman, WO, Roth, WT. Neurophysiological evidence of corollary discharge dysfunction in schizophrenia. Am J Psychiatry 2001;158:20692071. CrossRefGoogle Scholar
Farrer, C, Franck, N, Frith, CDet al. Neural correlates of action attribution in schizophrenia. Psychiatry Res 2004;131:3144. CrossRefGoogle Scholar
Fletcher, P, McKenna, PJ, Friston, KJ, Frith, CD, Dolan, JM. Abnormal cingulate modulation of fronto-temporal connectivity in schizophrenia. Neuroimage 1999;9:337342. CrossRefGoogle Scholar
Burns, J, Job, D, Bastin, MEet al. Structural disconnectivity in schizophrenia: a diffusion tensor magnetic resonance imaging study. Br J Psychiatry 2003;182:439443. CrossRefGoogle ScholarPubMed
Hubl, D, Koenig, T, Strik, Wet al. Pathways that make voices: white matter changes in auditory hallucinations. Arch Gen Psychiatry 2004;61:658668. CrossRefGoogle ScholarPubMed
Kubicki, M, Westin, CF, Maier, SEet al. Uncinate fasciculus findings in schizophrenia: a magnetic resonance diffusion tensor imaging study. Am J Psychiatry 2002;159:813820. CrossRefGoogle ScholarPubMed
Frith, C. Comments on Shaun Gallagher: neurocognitive models of schizophrenia: a neurophenomenological critique. Psychopathology 2004;37:2022. CrossRefGoogle Scholar
Spence, SA, Brooks, DJ, Hirsch, SR, Liddle, PF, Meehan, J, Grasby, PM. A PET study of voluntary movement in schizophrenic patients experiencing passivity phenomena (delusions of alien control). Brain 1997;120:19972011. CrossRefGoogle Scholar
Kopp, B, Rist, F. Error-correcting behaviour in schizophrenic patients. Schizophr Res 1994;13:1122. CrossRefGoogle ScholarPubMed
Shergill, SS, Samson, G, Bays, PM, Frith, CD, Wolpert, DM. Evidence for sensory prediction deficits in schizophrenia. Am J Psychiatry 2005;162:23842386. CrossRefGoogle Scholar