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Reduced 5-HT2A receptor binding after recovery from anorexia nervosa.

Biological psychiatry | Nov 1, 2002

http://www.ncbi.nlm.nih.gov/pubmed/12399143

BACKGROUND: Several lines of evidence suggest that a disturbance of serotonin neuronal pathways may contribute to the pathogenesis of anorexia nervosa (AN). This study applied positron emission tomography (PET) to investigate the brain serotonin 2A (5HT2A) receptor, which could contribute to disturbances of appetite and behavior in AN. METHODS: To avoid the confounding effects of malnutrition, we studied 16 women recovered from AN (REC AN, >1 year normal weight, regular menstrual cycles, no bingeing or purging) compared with 23 healthy control women (CW) using [18F]altanserin, a specific 5-HT2A receptor antagonist on PET imaging. RESULTS: REC AN women had significantly reduced [18F]altanserin binding relative to CW in mesial temporal (amygdala and hippocampus), as well as cingulate cortical regions. In a subset of subjects (11 CW and 16 REC AN), statistical parametric mapping (SPM) confirmed reduced mesial temporal cortex 5HT2A receptor binding and, in addition, showed reduced occipital and parietal cortex binding. CONCLUSIONS: This study extends research suggesting that altered 5-HT neuronal system activity persists after recovery from AN and may be related to disturbances of mesial temporal lobe function. Altered 5-HT neurotransmission after recovery also supports the possibility that this may be a trait-related disturbance that contributes to the pathophysiology of AN.

Pubmed ID: 12399143 RIS Download

Mesh terms: Adult | Anorexia Nervosa | Binding, Competitive | Brain | Cerebellum | Convalescence | Female | Fluorodeoxyglucose F18 | Humans | Ketanserin | Limbic System | Magnetic Resonance Imaging | Neural Pathways | Radiopharmaceuticals | Receptor, Serotonin, 5-HT2A | Receptors, Serotonin | Tomography, Emission-Computed

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Associated grants

  • Agency: NCRR NIH HHS, Id: 5 M01RR00084
  • Agency: NIMH NIH HHS, Id: R01 MH46001-07A1

NeuroSynth (Data, Activation Foci)

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