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Dopaminergic function in the psychosis spectrum: an [18F]-DOPA imaging study in healthy individuals with auditory hallucinations.

Oliver Howes, Paul Shotbolt, Michael Bloomfield, Kirstin Daalman, Arsime Demjaha, Kelly Diederen, Kemal Ibrahim, Euitae Kim, Philip Mcguire, René S. Kahn, Iris E C Sommer

Schizophrenia Bulletin January 26, 2012 DOI: 10.1093/schbul/sbr195 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Case-control study Peer reviewed
Sample size 32
Population 16 healthy individuals with frequent persistent auditory verbal hallucinations and 16 matched healthy controls
Keywords Brain Neostriatum Humans Hallucinations Fluorine radioisotopes Dopamine Positron-emission tomography Case-control studies Image processing, computer-assisted Adult Middle aged Female Healthy volunteers Schizophrenia Symptom Aetiology PET Neurochemistry Subclinical Psychosis continuum
Citations 94
Key findings Dopamine synthesis capacity in the striatum and its functional subdivisions did not differ significantly between healthy people with frequent persistent auditory verbal hallucinations and matched controls, and no relationship was found between subclinical psychotic symptom severity or schizotypal traits and dopamine synthesis capacity in the hallucinating group. The authors conclude that altered dopamine synthesis capacity is unlikely to underlie subclinical hallucinations, suggesting distinctions at the neurobiological level despite a possible phenomenological psychosis continuum.

Abstract

Background: The psychosis phenotype appears to exist in the population as a continuum, but it is not clear if subclinical psychotic symptoms and psychotic disorders share the same neurobiology. We investigated whether the dopaminergic dysfunction seen in psychotic disorders is also present in healthy, well-functioning people with hallucinations.

Methods: We compared dopamine synthesis capacity (using 6-[(18)F]fluoro-L-DOPA [[(18)F]-DOPA] positron emission tomography imaging) in 16 healthy individuals with frequent persistent auditory verbal hallucinations (hallucinating group) with that in 16 matched controls.

Results: There was no significant difference in dopamine synthesis capacity in the striatum, or its functional subdivisions, between groups and no relationship between subclinical psychotic symptom severity or schizotypal traits and dopamine synthesis capacity in the hallucinating group.

Conclusions: Altered dopamine synthesis capacity is unlikely to underlie subclinical hallucinations, suggesting that although there may be a phenomenological psychosis continuum, there are distinctions at the neurobiological level.

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