The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×
In This IssueFull Access

In This Issue

Clinical Guidance: ADHD and Its Treatment

The prevalence of ADHD in childhood has led to questions about the validity of the diagnosis and the long-term effects of the illness and its treatment. Articles in this issue indicate that the need for treatment lasts into adulthood and point to the increasing evidence for brain abnormalities in the illness. Persistence of ADHD and its association with mental illnesses in adulthood are well known in boys. Biederman et al. (CME, p. Original article: 409) extend this finding to girls. Over 40% of the girls were still receiving treatment in early adulthood, and there was increased incidence of antisocial personality disorder, mood and anxiety disorders, and other psychopathology (figure left). Ivanov et al. (p. Original article: 397) report that high-resolution images of the thalamus show deficits in children with both hyperactive and inattentive subtypes. Children who were treated with stimulant medication had smaller deficits than children who did not receive consistent treatment. In an editorial, Dr. Phillip Shaw (p. Original article: 363) points out that several studies have now shown that children who were treated for ADHD with psychostimulants have less brain volume loss than those who were untreated.

Cancer Gene Linked to Schizophrenia

A common variation in a gene that has the potential to promote cancer is less common in patients with schizophrenia than in healthy subjects. This protective variant of the MET proto-oncogene also influences neurodevelopment, and within the healthy subjects it was associated with higher cognitive ability. The study by Burdick et al. (p. Original article: 436) of variable DNA sequences in this gene stems from the lower incidence of cancer in schizophrenia patients than in the general population. Another region of the MET gene has previously been linked to autism.

Cognition in Families of African American Patients With Schizophrenia

A large study demonstrates that neurocognitive abilities in African Americans are inherited and are affected by schizophrenia, as they are in Caucasians. Calkins et al. (CME, p. Original article: 459) analyzed functioning in 10 neurocognitive domains for 610 African American patients with schizophrenia or schizoaffective disorder, their relatives, and community comparison subjects. The patients were slower and less accurate in most domains than their relatives—both with and without other psychiatric disorders—and the relatives were more impaired than the comparison subjects. These abilities may therefore provide quantifiable markers of schizophrenia, or endophenotypes, that could be used to identify individuals for genetics research.