Frontal responses during learning predict vulnerability to the psychotogenic effects of ketamine - Linking cognition, brain activity, and psychosis

被引:139
作者
Corlett, Philip R.
Honey, Garry D.
Aitken, Michael R. F.
Dickinson, Anthony
Shanks, David R.
Absalom, Anthony R.
Lee, Michael
Pomarol-Clotet, Edith
Murray, Graham K.
McKenna, Peter J.
Robbins, Trevor W.
Bullmore, Edward T.
Fletcher, Paul C.
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Psychiat, Cambridge CB2 2QQ, England
[2] Univ Cambridge, Sch Clin Med, Dept Psychiat, Brain Mapping Unit, Cambridge CB2 2QQ, England
[3] Univ Cambridge, Addenbrookes Hosp, Dept Anaesthesiol, Cambridge CB2 2QQ, England
[4] Univ Cambridge, Dept Expt Psychol, Cambridge CB2 2QQ, England
[5] UCL, Dept Psychol, London, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1001/archpsyc.63.6.611
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: Establishing a neurobiological account of delusion formation that links cognitive processes, brain activity, and symptoms is important to furthering our understanding of psychosis. Objective: To explore a theoretical model of delusion formation that implicates prediction error - dependent associative learning processes in a pharmacological functional magnetic resonance imaging study using the psychotomimetic drug ketamine. Design: Within-subject, randomized, placebo-controlled study. Setting: Hospital-based clinical research facility, Addenbrooke's Hospital, Cambridge, England. The work was completed within the Wellcome Trust and Medical Research Council Behavioral and Clinical Neuroscience Institute, Cambridge. Participants: Fifteen healthy, right-handed volunteers (8 of whom were male) with a mean +/- SD age of 29 +/- 7 years and a mean +/- SD predicted full-scale IQ of 113 +/- 4 were recruited from within the local community by advertisement. Interventions: Subjects were given low-dose ketamine (100 ng/mL of plasma) or placebo while performing a causal associative learning task during functional magnetic resonance imaging. In a separate session outside the scanner, the dose was increased (to 200 ng/mL of plasma) and subjects underwent a structured clinical interview. Main Outcome Measures: Brain activation, blood plasma levels of ketamine, and scores from psychiatric ratings scales (Brief Psychiatric Ratings Scale, Present State Examination, and Clinician-Administered Dissociative States Scale). Results: Low-dose ketamine perturbs error-dependent learning activity in the right frontal cortex (P = .03). Highdose ketamine produces perceptual aberrations (P = .01) and delusion-like beliefs (P = .007). Critically, subjects showing the highest degree of frontal activation with placebo show the greatest occurrence of drug-induced perceptual aberrations (P = .03) and ideas or delusions of reference (P = .04). Conclusions: These findings relate aberrant prediction error - dependent associative learning to referential ideas and delusions via a perturbation of frontal cortical function. They are consistent with a model of delusion formation positing disruptions in error-dependent learning.
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收藏
页码:611 / 621
页数:11
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