Disrupted Reinforcement Signaling in the Orbitofrontal Cortex and Caudate in Youths With Conduct Disorder or Oppositional Defiant Disorder and a High Level of Psychopathic Traits

Youths with conduct disorder and oppositional defiant disorder show high rates of aggressive and antisocial behaviors (1). A subset of these youths also display callousness and psychopathic traits, including lack of guilt, empathy, and remorse (2, 3). This subset of youths is at highest risk for recurrent antisocial acts and future criminal behaviors (3–6). While psychopathic traits are detectable early in childhood and persist into adulthood (7), little is known about the pathophysiology (8–10).

The presence of psychopathic traits has long been linked to problems in emotional learning (11, 12). Specifically, it has been argued that these traits reflect impairment in stimulus-reinforcement learning and in decision making (13, 14). An early task indexing this impairment was the passive avoidance task (11, 15, 16). Passive avoidance tasks require participants to learn to respond to (i.e., approach) stimuli that engender reward and refrain from responding to (i.e., passively avoid) stimuli that engender punishment. Adults and youths with psychopathic traits show a deficient capability to learn to avoid the stimuli that predict punishment regardless of whether the punishment is shock, loss of money, or loss of points (11, 15, 16).

Passive avoidance learning tasks are particularly informative, as both electrophysiologic and lesion studies map its neural basis, implicating the amygdala, orbitofrontal cortex, and striatum (17–21). In addition, a functional magnetic resonance imaging (fMRI) study of a passive avoidance task has confirmed the importance of these regions in healthy human adults (22). It is argued that the amygdala allows the formation of stimulus-reinforcement associations, determining which of the stimuli are “good” and which “bad,” and that this information is fed forward as reinforcement expectations to the orbitofrontal cortex (19–21), potentially via the ventral striatum (23). The orbitofrontal cortex is critical for the representation of this reinforcement-expectation information, thereby facilitating successful decision making (24, 25). The orbitofrontal cortex and caudate are also critical for error prediction, which facilitates learning of reward or punishment contingencies (26–28). The detection of prediction errors prompts enhanced reinforcement-based learning (29). These prediction errors are maximal after the individual's first exposure to the cue and reinforcement but rapidly lessen (unless the reinforcement contingency changes) as the individual develops an expectation of the reinforcement associated with the cue (29).

Originally, the deficits shown by individuals with psychopathic traits on passive avoidance tasks were attributed to less processing of punishment information (11). However, work has shown that individuals with psychopathic traits appropriately use punishment information to modify responses immediately following an error. Instead, it is argued that the deficits arise from impairment in the formation and use of stimulus-reinforcement associations in decision making (30). The individual with psychopathic traits is less able to use reinforcement information to change his or her representation of the outcome associated with the response and consequently is less able to use reinforcement expectancies to guide behavior (13). A deficit in stimulus-reinforcement processing is thought to result from dysfunction in the integrated functioning of the amygdala and orbitofrontal cortex (13). In line with this model, recent fMRI work has indicated less amygdala responding and less amygdala-orbitofrontal cortex functional connectivity in response to fearful expressions in youths with psychopathic traits than in comparison subjects (8, 9). Moreover, anomalous neural responses in the orbitofrontal cortex to reversal errors have also been identified in this population (10).

The goal of the current study was to assess the nature of the functional irregularities within the amygdala, orbitofrontal cortex, and striatum of youths with conduct disorder or oppositional defiant disorder plus psychopathic traits. Specifically, the study tested three hypotheses. First, we hypothesized that early reinforcement processing would be abnormal in these youths. For initial exposures to reinforced outcomes, prediction errors are high; the participant has no reinforcement expectancy associated with the stimulus, and thus all reinforcement received is unexpected (29). Healthy individuals show marked increases in activity, particularly within the orbitofrontal cortex and striatum, in response to unexpected reinforcements (26–28). We predicted, however, that this initial heightened responding to early trials would not be seen in the subjects with conduct disorder or oppositional defiant disorder plus psychopathic traits, at least within the orbitofrontal cortex. Our second hypothesis was that the signaling associated with reward and punishment outcomes would be abnormal in this group. Several studies have documented heightened responses to rewarded relative to punished outcomes within the amygdala, orbitofrontal cortex, and striatum during decision making (23, 24, 31). We predicted that this heightened responding to rewarded outcomes would be seen only in the healthy youths and not in those with conduct disorder or oppositional defiant disorder plus psychopathic traits.

Method

Participants

Thirty youths participated in this study: 15 youths with psychopathic traits and either conduct disorder or oppositional defiant disorder and 15 healthy comparison youths (Table 1). Youths were recruited from the community through newspaper ads, fliers, and referrals from mental health practitioners in the area. Statements of informed assent and consent were obtained from the participating children and parents. This study was approved by the institutional review board of the National Institute of Mental Health.

All youths and parents completed the Schedule for Affective Disorders and Schizophrenia for School-Age Children—Present and Lifetime Version (K-SADS-PL) (33) with an experienced clinician trained and supervised by expert child psychiatrists, with good interrater reliability (kappa higher than 0.75 for all diagnoses). IQ was assessed with the Wechsler Abbreviated Scale of Intelligence (two-subtest form). The exclusion criteria were pervasive developmental disorder, Tourette's syndrome, depression, bipolar disorder, generalized, social, or separation anxiety disorder, posttraumatic stress disorder, neurologic disorder, lifetime history of psychosis, history of head trauma, and an IQ under 80. In addition, the parents also completed the Antisocial Process Screening Device (32), a measure of psychopathic traits. Youths meeting the K-SADS-PL criteria for conduct disorder or oppositional defiant disorder who had scores of 20 or higher on the Antisocial Process Screening Device returned to complete the Psychopathy Checklist: Youth Version (5). Youths scoring 20 or higher on this instrument were included in the psychopathic traits group; those scoring less than 20 were excluded from the study. The comparison subjects did not meet the criteria for any K-SADS-PL diagnosis and scored below 20 on the Antisocial Process Screening Device.

Clinical Measures

Antisocial Process Screening Device.

This is a 20-item parent-completed rating of callous-unemotional traits and conduct and impulsivity problems (32), designed to detect antisocial processes in youths. A three-factor structure has been characterized and comprises the following dimensions: callous/unemotional, narcissism, and impulsivity (32). There is no established cutoff score for classification of a high level of psychopathic traits (32, 34, 35). For research purposes, studies of adolescents have used a cutoff score of 20 (8, 10, 36), median splits (higher than 11 for males, 9 for females) (37), or percentile rankings (top one-third, score above 18) (35). Following our previous work (8, 10), we used a score of 20 or higher in this study. All of the healthy comparison subjects scored less than 15 on this measure.

Psychopathy Checklist: Youth Version.

This is a 20-item rating scale for assessing interpersonal, affective, and behavioral features related to psychopathic traits in adolescents (5). It is based on a semistructured interview and collateral information. A score of 20 or higher was used to define the group with high levels of psychopathic traits (8, 10), as there are no standard cutoff scores for classifying youths on this measure to date (5).

The fMRI passive avoidance task.

A modified version of the previously reported fMRI passive avoidance task was used (Figure 1) (22, 38). The characteristics of the task were equivalent to those used in a previous study (38) with the exception that eight stimuli, rather than 12, were presented in each fMRI run. Each of the four runs involved a new set of eight stimuli for the participant to learn about. Trials began with the presentation for 1,100 msec of one of these eight stimuli (Snodgrass line drawings [39] on a black background). Button press responses to four of the stimuli engendered a reward (“You WIN 100 points”). Button presses in response to the other four stimuli engendered punishment (“You LOSE 100 points”). If no response was made, a fixation cross was presented in lieu of reinforcement. The reinforcement phase (reward, punishment, or fixation cross) lasted for 1,000 msec. Following this, there was a 200-msec fixation cross before the commencement of the next trial. The participant's goal was to win as many points as possible; the subject had to learn to respond to the stimuli engendering reward and withhold from responding to the stimuli engendering punishment.

The stimuli were presented in random order once per block for eight acquisition blocks. After the eight acquisition blocks, the reinforcement value associated with one-half of the stimuli changed (this extinction component of the study will be considered in a separate article). Within each block of eight stimuli, there were an additional four fixation point trials (with 2,300 msec of the fixation point) to serve as a baseline. Each of the fMRI runs contained a different set of eight stimuli.

Each participant completed a brief practice session and then four runs of the task in a scanner. Four versions of the task were developed to counterbalance the reinforcements associated with each of the stimuli. The task version and run order were randomized across participants.

MRI Characteristics

During task performance the participants were scanned with a 3.0-T GE Signa scanner (GE Healthcare Systems, Fairfield, Conn.). A total of 189 functional images per run were taken with a gradient echo planar imaging (EPI) sequence, with a repetition time of 2,300 msec, echo time of 23 msec, 64×64 matrix, flip angle of 90°, and 24-cm field of view. Whole-brain coverage was obtained with 34 axial slices (thickness, 3.3 mm). A high-resolution anatomical scan (three-dimensional fast spoiled gradient echo sequence; repetition time=6 msec, echo time=2.5 msec, field of view=24 cm, flip angle=12°, 124 axial slices, thickness=1.0 mm, 224×224 matrix) in register with the EPI data set and covering the whole brain was obtained.

Imaging Data Preprocessing

Imaging data were preprocessed and analyzed with AFNI software (40). At the individual level, functional images from the first five volumes of each run, collected before equilibrium magnetization was reached, were discarded. Functional images from the four time series were motion corrected and spatially smoothed with a 6-mm full-width half-maximum Gaussian filter. The time series were normalized by dividing the signal intensity of a voxel at each time point by the mean signal intensity of that voxel for each run and multiplying the result by 100. The resultant regression coefficient represented a percentage signal change from the mean.

Following this, regressors characterizing the trial and response types were generated: correct hits (responses to stimuli associated with reward), commission errors (responses to stimuli associated with punishment), correct avoidances (no response to stimuli associated with punishment), and omission errors (no response to stimuli associated with reward). To examine differential responsiveness to initial exposures, as opposed to later learning, we evaluated neural responses during the exposures to the stimulus-reinforcement associations in block 1 in comparison to exposures in blocks 2–8.

All regressors were created by convolving the train of stimulus events with a gamma-variate hemodynamic response function to account for the slow hemodynamic response. Linear regression modeling was performed by using the aforementioned regressors plus regressors to model a first-order baseline drift function. This produced a beta coefficient and associated t statistic for each voxel and regressor. In accordance with findings that normalization of brain volumes from age 7–8 years onward does not introduce major age-related distortions in localization or time course of the blood-oxygen-level-dependent (BOLD) signal in event-related fMRI (41, 42), the participants' anatomical scans were individually registered to the Talaraich and Tournoux atlas (43). The individuals' functional imaging data were then registered to their Talaraich-fit anatomical scans within AFNI.

fMRI Data Analysis

The group analysis of the BOLD data was then performed on the regression coefficients from the analyses for the individual subjects by means of a 2×2×2 analysis of variance (ANOVA). The three variables were diagnosis (psychopathic traits versus comparison subjects), response type (correct hits versus commission errors), and learning phase (early [block 1] versus late [blocks 2–8]). The initial probability threshold was set at p<0.005 (corrected at p<0.05 for multiple comparisons). Extent-threshold correction for multiple comparisons was done by using the AlphaSim program in AFNI. Average percentage signal change was measured within each significant cluster of 547 mm³ or greater. Post hoc analysis of significant interactions was performed with planned ANOVAs within SPSS (SPSS, Chicago).

Results

Behavioral Results

There were no significant group differences in age or IQ (Table 1). The 2×2×2 analysis of group differences in -omission and commission errors revealed the expected interaction of diagnosis, learning phase, and error type (F=4.6, df=1, 28, p<0.05). The youths with conduct disorder or oppositional defiant disorder plus psychopathic traits made significantly more commission errors than the comparison subjects during the late learning phase (F=5.4, df=1, 28, p<0.05) (Figure 2); the mean numbers of commission errors per block in the early phase were 3.31 (SD=0.39) and 3.65 (SD=0.62), respectively, and during the late phase the mean numbers were 1.15 (SD=0.79) and 0.05 (SD=0.23). There was also a significant interaction of diagnosis and learning phase (F=10.5, df=1, 28, p<0.005); the youths with psychopathic traits made significantly more errors during the late learning phase than the comparison subjects (F=7.4, df=1, 28, p<0.01). There was no main effect of diagnosis.

fMRI Results

The goal of the current study was to assess the nature of the functional irregularities within the amygdala, orbitofrontal cortex, and striatum in youths with conduct disorder or oppositional defiant disorder plus psychopathic traits during passive avoidance learning. We examined this issue through a 2×2×2 ANOVA conducted on the BOLD response data, with diagnosis (conduct disorder or oppositional defiant disorder plus psychopathic traits versus comparison subjects), learning phase (early or late: block 1 versus blocks 2–8), and response type (commission error versus correct hit) (Table 2). The key interactions with respect to our predictions (diagnosis-by-phase and diagnosis-by-response interactions) and the main effect of diagnosis are described in the following to provide results for the test of our a priori hypotheses. No significant finding occurred for the three-way diagnosis-by-phase-by-response interaction.

Our first interaction of interest, the diagnosis-by-phase interaction, examined whether the youths with conduct disorder or oppositional defiant disorder plus psychopathic traits showed atypical BOLD responses during early trial learning. In line with predictions, significant diagnosis-by-phase interactions were observed within the orbitofrontal cortex and the caudate (although not within the amygdala). In addition, significant diagnosis-by-phase interactions were seen in a network of attentional regions, including the inferior frontal cortex, middle frontal gyrus, and inferior parietal lobule (Table 2). In all the regions identified by this interaction, the comparison subjects showed greater activity during the early, but not late, trials relative to the youths with a disruptive behavior disorder plus psychopathic traits. Findings for the orbitofrontal cortex (Brodmann's area 11) (early: t=3.2, df=28, p<0.005; late: n.s.) and the caudate (early: t=4.2, df=28, p<0.001; late: n.s.) are shown in Figure 3.

Our second interaction of interest, the diagnosis-by-response type interaction, examined whether the youths with a behavior disorder plus psychopathic traits showed atypical BOLD responses to rewarded correct hits relative to the responses to punished commission errors. Significant diagnosis-by-response type interactions were observed within an anterior region of the orbitofrontal cortex, middle frontal gyrus, and parahippocampal gyrus (Table 2). Within the orbitofrontal cortex, the youths with psychopathic traits showed less activation during rewarded correct hits than the comparison subjects (F=4.6, df=1, 29, p<0.05) (Figure 4), while the responses during punished commission errors were comparable (F<1.0, df=1, 29, p=0.82). In contrast, in the left middle frontal and right parahippocampal gyrus, the comparison subjects showed greater activation during commission errors than did the youths with a behavior disorder plus psychopathic traits (left middle frontal gyrus: F=14.2, df=1, 29, p<0.001; right parahippocampal gyrus: F=5.4, df=1, 29, p<0.05), while activation during correct hits was comparable in the two groups (F<1.0, df=1, 29).

In addition, there was a significant main effect of diagnosis within the amygdala, caudate, insula, and a network of regions implicated in attention processes, including the dorsolateral prefrontal cortex and parietal cortex (Table 2, figure in online data supplement). In all of these regions, the youths with a behavior disorder plus psychopathic traits showed significantly less activation than the comparison subjects.

To account for possible effects of medication use on the BOLD responses, the preceding analysis was repeated without the seven youths in the group with psychopathic traits who were taking medication and their seven age- and IQ-matched comparison subjects. The preceding effects of interest were replicated. Thus, the diagnosis-by-phase interaction was replicated in the middle orbitofrontal cortex; the group with psychopathic traits showed less early activation than the comparison subjects. Similarly, the diagnosis-by-response type interaction was observed in the orbitofrontal cortex. Moreover, the main effects of diagnosis in the amygdala, caudate, and dorsolateral prefrontal cortex again revealed less activation in the youths with conduct disorder or oppositional defiant disorder plus psychopathic traits than in the comparison subjects.

Discussion

The goal of the current study was to assess the nature of the irregularities within the amygdala, orbitofrontal cortex, and striatum in youths with conduct disorder or oppositional defiant disorder plus psychopathic traits during passive avoidance learning. Specifically, this study examined group differences in neural responses to two features critical to emotional learning: the level of experience with the stimulus (early versus late trials) and the type of response and reinforcement (rewarded correct responses versus punished incorrect responses). The results revealed that the youths with psychopathic traits, relative to healthy youths, showed significantly less activity within the orbitofrontal cortex and caudate in response to early exposures to reinforced outcomes. Moreover, in response to rewarded correct responses, the group with psychopathic traits showed significantly less activity within the orbitofrontal cortex than did the comparison youths. These task measures did not reveal group differences within the amygdala, although the group with psychopathic traits had generally lower activity within this region across the task.

Impairments in passive avoidance have been repeatedly reported in individuals with psychopathic traits (11, 15, 16, 44). Our model of passive avoidance learning and its dysfunction in individuals with psychopathic traits is highly influenced by the work of Schoenbaum, Gallagher, and colleagues (19, 45, 46). In essence, we assume that in healthy individuals prediction errors in response to unexpected reinforcements (mediated by the orbitofrontal cortex and caudate) serve to initiate rapid stimulus-reinforcement learning in the amygdala. As learning progresses, more accurate reinforcement expectancies are fed from the amygdala to the orbitofrontal cortex, where their representation allows successful decision making to occur, initiating approaches to objects associated with reward and avoidance of those associated with punishment. In individuals with high levels of psychopathic traits, deficits in prediction error signaling lead to slower and weaker stimulus-reinforcement learning, which in turn leads to weaker and less accurate reinforcement expectancies being fed forward to the orbitofrontal cortex. Individuals become progressively less accurate in their decisions relative to comparison individuals because they are less able to represent the reward expectancy value associated with the presented stimulus and respond accordingly (13).

Previous work has indicated dysfunction of the orbitofrontal cortex in individuals with psychopathic traits (47, 48). The current study extends this by providing information on the nature of the functional impairment. In line with the model, youths with conduct disorder or oppositional defiant disorder plus psychopathic traits, relative to comparison youths, showed significantly lower orbitofrontal cortex responses during early trial learning and to rewarded responses. The first of these findings is compatible with the suggestion of disrupted prediction error signaling in the orbitofrontal cortex in the youths with psychopathic traits (see reference 28). Prediction errors are maximal after the individual's first exposure to the relationship between the cue and the reinforcement but rapidly lessen as the individual develops an expectation of the reinforcement associated with the cue (29). In this regard it is notable that we have previously documented lower orbitofrontal cortex responses, relative to those in comparison groups, to unexpected failures to receive rewards in children with conduct disorder or oppositional defiant disorder plus psychopathic traits (10). The finding of lower orbitofrontal cortex responses to rewarded responses is consistent with the suggestion that this population is less able to represent reward expectancy values. As such, these data are consistent with results from a previous study examining youths with conduct disorder, undifferentiated by psychopathic traits (49). This study also showed lower responsiveness to reward outcome information within the orbitofrontal cortex in the youths with conduct disorder.

Neurobiological accounts of psychopathic traits (13, 50, 51) have neglected consideration of the caudate (and for that matter, the ventral tegmental area and ventral striatum), despite the critical role of these regions in prediction error signaling and/or reinforcement-based learning (26, 27, 52). Part of this likely reflects the choice of cognitive functions examined in the majority of previous fMRI work with youths or adults with psychopathic traits, i.e., expression processing (8, 9, 53), emotional memory (54), and moral reasoning (55). However, the current study revealed lower responsiveness in the caudate (but not the ventral tegmental area or ventral striatum) to early reinforced outcomes relative to later trials in the youths with psychopathic traits. This is compatible with the suggestion of disrupted prediction error signaling in the caudate in youths with conduct disorder or oppositional defiant disorder plus psychopathic traits. Indeed, it is notable that the only previous study examining operant responding in individuals with psychopathic traits also showed dysfunctional responding to reversal errors in the caudate but not ventral striatum among children with conduct disorder or oppositional defiant disorder plus psychopathic traits (10). This pattern is echoed by recent structural MRI work also indicating selective structural abnormalities within the dorsal striatum in adults with psychopathic traits (56). A recent study of healthy adults focused on the nucleus accumbens and found that individuals scoring higher on the impulsive aggressivity components of the Psychopathic Traits Inventory had greater pharmacologically triggered dopamine release and greater activity in response to reward (57). Although intriguing results, these data were somewhat inconsistent with those from the only previous study of which we are aware that showed ventral striatal abnormalities in adults meeting criteria for psychopathy (54). This latter study showed lower ventral striatum activity in response to emotional stimuli in the adults with psychopathy—albeit in response to a very different task. The current study also did not identify any regions demonstrating greater activity during rewarding trials in the youths with psychopathic traits. These differences may reflect the hypothesized distinction between individuals showing heightened aggressive impulsivity in the absence of the core callous traits of psychopathy (who are believed to demonstrate heightened limbic responsiveness [14]) and those who do show these core callous traits (who show low limbic responsiveness).

The dorsal anterior cingulate cortex has been implicated in conflict monitoring (58) and the use of error signals and the integration of reinforcement history to select between competing responses (59, 60). The current study was not designed to distinguish between these models. However, it is important to note that the significant main effect of response type, i.e., commission error versus correct hit, identified in this region (see table in online data supplement) was not modulated by a main effect of group or a group-by-response type interaction. These data suggest that the responses of the dorsal anterior cingulate cortex to the conflict initiated by punishment/error feedback remain intact in youths with conduct disorder or oppositional defiant disorder plus psychopathic traits. Notably, this replicates prior results in similar subjects during a reversal learning paradigm, where both groups showed appropriate recruitment of the dorsal anterior cingulate cortex in response to punished reversal errors (10). In contrast, functional (10) and now structural (56) abnormalities have been reported in these populations in the dorsal striatum (caudate), indicating that abnormalities in reward processing may arise from deficits in the amygdala-insula-orbitofrontal-caudate circuit.

The main effect of diagnosis revealed reduced activation in several brain regions in the youths with psychopathic traits. This could indicate less engagement with the task. In contrast, the regions showing a main effect of response type and phase (i.e., regions where both groups showed appropriate responses as a function of task measures) include the dorsal anterior cingulate cortex and inferior frontal cortex/anterior insula. It is important to note that these data suggest that an engagement explanation appears unsatisfactory, as there is no reason why less task engagement would lead to appropriate recruitment of systems necessary for response change but selectively less recruitment of regions implicated in decision making based on stimulus reinforcement.

One caveat of the present study is that although there were high rates of comorbidity of attention deficit hyperactivity disorder (ADHD) with conduct disorder and oppositional defiant disorder, we did not include a second ADHD comparison group in the current study because neither of our previous studies indicated that youths with ADHD have pathophysiology in the amygdala or orbitofrontal cortex, although this was seen in children with conduct disorder or oppositional defiant disorder plus psychopathic traits (8, 10). Rubia and colleagues have shown dysfunction in orbitofrontal cortex reward signaling in youths with conduct disorder who do not have ADHD but not in youths with ADHD (49). Second, the youths with conduct disorder or oppositional defiant disorder plus psychopathic traits made significantly more commission errors during the late learning phase, which could produce stronger parameter estimates for late commission errors for this group. However, it should be noted that the groups differed not in BOLD responses to late commission errors but, rather, in responses during early trials and in responses to rewarded correct hits.

In short, the current results are highly compatible with developmental models of conduct disorder with psychopathic traits that stress that this disorder reflects a fundamental disruption in the neural systems necessary for appropriate decision making in regard to stimulus reinforcement (14). Problems in this basic form of emotional learning will create difficulties for the child in socializing; the child will be less likely to “learn from his or her mistakes.” Moreover, children will learn from emotional feedback more slowly—this is notable in the present study both in the behavioral data and in the lower sensitivity within both the orbitofrontal cortex and the caudate to early reinforcement information. Appropriate representation of such information is critical for rapid, early emotional learning. In addition, the dysfunction in the signaling of reinforcement outcomes in the orbitofrontal cortex, documented in this study, will be associated with poor decision making. This will lead to the selection of nonoptimal behavioral choices (actions that harm others and actions that are likely to result in individuals being frustrated and potentially reactively aggressive because they do not meet their goals).

These data have clear treatment implications. Specifically, they suggest that the development of pharmacologic or behavioral therapeutic approaches that augment the capacity to make decisions based on stimulus reinforcement may enable youths with high levels of psychopathic traits to overcome their functional deficiencies. In this regard, it is notable that both serotonergic (61) and dopaminergic (62) manipulations influence the performance of the task described in this study as well as its neural substrates. Moreover, a recent report indicated that prediction error signaling in the amygdala facilitates learning by increasing orienting and attention to the stimulus during the subsequent trial (63), and an interesting behavioral approach might be to train youths to direct their attention to explicitly form predictions about the expected reward from a particular action and to explicitly attend to the difference between their verbalized prediction and the actual outcome for both advantageous and disadvantageous actions.

In summary, the current data support previous suggestions of dysfunction in the amygdala and orbitofrontal cortex in youths with conduct disorder or oppositional defiant disorder plus psychopathic traits. More important, they indicate that such individuals are marked by a compromised sensitivity to early reinforcement information in both the orbitofrontal cortex and caudate and to reward outcome information within the orbitofrontal cortex. In conjunction with established models of stimulus-reinforcement instrumental learning, they suggest that the integrated functioning of the amygdala, caudate, and orbitofrontal cortex may be disrupted in individuals with conduct disorder or oppositional defiant disorder plus psychopathic traits.