Abstract | BACKGROUND: METHODS: Approximately 24 hours after injection of [123I]-2beta-carbomethoxy-3beta-(4-iodophenyl)tropane ([123I] beta-CIT), single photon emission computed tomography scans were performed in 10 medication-free, female bulimic patients and 10 age-matched, healthy females. For quantification of brain serotonin transporter and dopamine transporter availability, a ratio of specific to nonspecific [123I] beta-CIT brain binding was used (V(3)" = target region - cerebellum/cerebellum). RESULTS: Drug-free bulimia nervosa patients showed a 17% reduced brain serotonin transporter availability in the hypothalamus and thalamus, as compared with healthy control subjects (2.4 +/- 0.4 vs. 2.9 +/- 0.4, p =.026), and a similar reduction in striatal dopamine transporter availability. There was a negative correlation of illness duration and serotonin transporter availability (r = -.65; p =.042) and a strong positive correlation between hypothalamic/thalamic and striatal V(3)" (r =.80, p <.001). CONCLUSIONS: This first report of reduced [123I] beta-CIT binding in a relatively small group of patients with bulimia nervosa suggests a reduced hypothalamic and thalamic serotonin transporter availability in bulimia, which is more pronounced with longer duration of illness.
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Authors | J Tauscher, W Pirker, M Willeit, M de Zwaan, U Bailer, A Neumeister, S Asenbaum, C Lennkh, N Praschak-Rieder, T Brücke, S Kasper |
Journal | Biological psychiatry
(Biol Psychiatry)
Vol. 49
Issue 4
Pg. 326-32
(Feb 15 2001)
ISSN: 0006-3223 [Print] United States |
PMID | 11239903
(Publication Type: Journal Article)
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Chemical References |
- Carrier Proteins
- Radiopharmaceuticals
- Serotonin
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Topics |
- Adolescent
- Adult
- Binding, Competitive
(physiology)
- Biological Transport, Active
(physiology)
- Brain
(metabolism)
- Bulimia
(metabolism, therapy)
- Carrier Proteins
(metabolism)
- Cerebellum
(metabolism)
- Cognitive Behavioral Therapy
- Depression
(diagnosis, psychology)
- Female
- Humans
- Radiopharmaceuticals
- Serotonin
(metabolism)
- Tomography, Emission-Computed, Single-Photon
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