Abstract
Objectives. Bulimia nervosa (BN) is associated with abnormalities of serotoninergic system. Functional or ligand specific brain imaging studies revealed abnormalities in non-overlapping regions. [18F]MPPF (4-(2-methoxyphenyl)-1-[2-(N-2-pyridinyl)-p-fluorobenzamido]-ethylpiperazine) is a selective 5-HT1A receptor antagonist with a serotonin-like affinity, capable to assess changes of brain serotoninergic activity in BN patients. Methods. [18F]MPPF cerebral binding potential (BPND) was measured by positron emission tomography scan in nine purging-type BN patients and eleven age-matched controls. Voxel-based statistical parametric mapping (SPM) analyses were performed to assess BPND differences between the two groups and between each BN patient and controls group. Results. Mean [18F]MPPF BPND was overall increased in BN patients. SPM analysis with revealed symmetrical large clusters of increased [18F]MPPF binding in insula, temporo-parietal cortex, prefrontal cortex, in limbic, paralimbic cortex and raphe nuclei. SPM individual analysis indicated significant heterogeneity of [18F]MPPF mapping within BN group, including cases with isolated up to widespread increased binding. [18F]MPPF BPND did not covariate with depression or eating behaviour-related scores. Conclusions. Large clusters of increased [18F]MPPF binding in severe BN overlap previous results, separately described within fMRI or PET studies. The relationship between the inter-individual [18F]MPPF binding heterogeneity and serotoninergic modulators efficacy in these patients remains to be assessed.
Acknowledgements
This work was supported by grant no. A01041KS from ATC (Action Thématique Concertée) Nutrition, France.
Statement of interest
None to declare.