In this study, no changes in cortical 5-HT
2A receptor binding, assessed by
123I-5-I-R91150 and SPECT, were observed in acutely ill bulimia nervosa patients, relative to healthy comparison subjects. In addition, a significantly negative relationship between binding index and age in the prefrontal cortex indicated that in bulimia nervosa patients, as well as in healthy subjects, an age-related decline in 5-HT
2A receptor availability was preserved. These results agree with those of the literature
+(5). In a previous (indirect) study, no significant difference in CSF levels of 5-hydroxyindoleacetic acid (5-HIAA) was found between bulimia nervosa patients and healthy comparison subjects
+(6). This finding could indicate that central 5-HT turnover is not disturbed in acutely ill bulimia nervosa patients. Yet, in another study using [
123I]β-CIT and SPECT, a reduction of available binding sites in 5-HT transporter-rich areas was documented in 10 medication-free female patients with bulimia, compared with 10 age-matched healthy female subjects
+(7). Although decreased [
123I]β-CIT binding may reflect central 5-HT dysfunction, secondary changes may involve the postsynaptic 5-HT
2A receptor as well. In a positron emission tomography study that used [
18F]altanserin, a ligand for the postsynaptic 5-HT
2A receptor, reduced binding in the orbital frontal cortex was found in patients who recovered from bulimia nervosa
+(8). Based on the observation that recovered bulimia nervosa patients have elevated CSF 5-HIAA concentrations
+(9) and in agreement with in vitro studies
+(10), the authors postulated that 5-HT
2A receptors were down-regulated. Based on our findings, acutely ill bulimia nervosa patients are not characterized by altered cortical 5-HT
2A receptor binding in specific (prefrontal) brain regions. These results clearly differ from those in acutely ill anorexia nervosa patients
+(3), suggesting that different biological mechanisms are involved in patients with different types of eating disorders.