No abstract

Adolescent risk taking has been known to increase in the presence of peers. We hypothesized that peer interaction reduces the activation of the medial prefrontal cortex (mPFC) that is required for self-regulation of reward-driven behavior. We also expected that mPFC activity would be reduced more in those with greater surgency, a composite trait of behavioral approach, sensation seeking and positive affect. In our study, 20 15-year-old boys played a simulated driving video game alone and in the presence of peers who were encouraged to call out advice while we recorded the feedback-related negativity (FRN) event-related potential in response to an impending car crash. FRN amplitude was reduced both as a function of peer presence and increased surgency. More importantly, we also calculated intracerebral current source density at the time of the FRNs, and found that both greater surgency and peer presence are associated with reduced activity specifically in the mPFC. Riskier performance resulting in more car crashes resulted from the presence of peers only as an interaction with surgency, this interaction being related strongly to reduced activity in the ventromedial PFC.

The short form of the Conners-Wells Adolescent Self-Report Scale (CASS:Short) is administered to 319 children and 844 adolescents to investigate whether the instrument can be used with respondents under the age of 12. Mothers of all respondents are asked to rate each child using a measure designed to assess a parallel set of problem behaviors. The factor structure of the CASS:Short is tested in both samples and is found to have good fit to the data. Mean levels of ADHD symptomatology are also examined for possible sex and age effects, as was the relationship between parent and self-report ratings. The overall results provide empirical support for the use of the CASS:Short with children ages 7 to 11.

CORRESPONDENCE mentioned once, but the term dysphoria is never used. King et a! have contributed important informa tion regarding the disturbing incidence of dysphoria without akathisia in normal subjects given oral haloperidol 5 mg.