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Dopamine synthesis capacity in patients with treatment-resistant schizophrenia

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)1203-1210
Number of pages8
JournalThe American Journal of Psychiatry
Issue number11
PublishedNov 2012

King's Authors


Objective: Elevated presynaptic striatal dopaminergic function is a robust feature of schizophrenia. However, the relationship between this dopamine abnormality and the response to dopamine-blocking antipsychotic treatments is unclear. The authors tested the hypothesis that in patients with schizophrenia the response to antipsychotic treatment would be related to the severity of presynaptic dopamine dysfunction, as indexed using [F-18]-DOPA uptake positron emission tomography (PET).

Method: Twelve patients with treatmentresistant schizophrenia, twelve patients with schizophrenia who had responded to antipsychotics, and twelve healthy volunteers matched for gender, age, ethnicity, weight, and cigarette smoking underwent [F-18]-DOPA PET scanning. [F-18]-DOPA influx rate constants Nicer values) were measured in the striatum and its functional subdivisions.

Results: Patients who had responded to antipsychotic treatment showed significantly higher Kicer striatal values than did patients with treatment-resistant illness (effect size=1.11) and healthy volunteers (effect size=1.12). The elevated [F-18]-DOPA uptake was most marked in the associative (effect size=1.31) and the limbic (effect size=1.04) striata I subdivisions. There were no significant differences between patients with treatment-resistant illness and healthy volunteers in the whole striatum or any of its subdivisions.

Conclusions: In some patients with schizophrenia, antipsychotic treatment may be ineffective because they do not exhibit the elevation in dopamine synthesis capacity that is classically associated with the disorder; this may reflect a different underlying pathophysiology or a differential effect of antipsychotic treatment.

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