4.7 Article

Dopaminergic Activity in Antipsychotic-Naive Patients Assessed With Positron Emission Tomography Before and After Partial Dopamine D2 Receptor Agonist Treatment: Association With Psychotic Symptoms and Treatment Response

Journal

BIOLOGICAL PSYCHIATRY
Volume 91, Issue 2, Pages 236-245

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2021.08.023

Keywords

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Funding

  1. Mental Health Services in the Capital Region of Denmark
  2. Faculty of Health and Medical Sciences, University of Copenhagen
  3. Lundbeck Foundation to the Lundbeck Foundation Centre of Excellence for Clinical Intervention and Neuropsychiatric Schizophrenia Research [R155-2013-16337]
  4. WOrzner Foundation
  5. Gerhard Lind Foundation
  6. Mental Health Services, Capital Region of Denmark
  7. Lundbeck Foundation
  8. University of Copenhagen

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High baseline decarboxylation rates were associated with more positive symptoms at baseline and with symptom improvement after treatment. Specific parameters for the putamen and nucleus accumbens were associated with psychotic symptoms.
BACKGROUND: Dopamine activity has been associated with the response to antipsychotic treatment. Our study used a four-parameter model to test the association between the striatal decarboxylation rate of F-18-DOPA to F-18 dopamine (k(3)) and the effect of treatment on psychotic symptoms in antipsychotic-naive patients with first episode psychosis. We further explored the effect of treatment with a partial dopamine D-2 receptor agonist (aripiprazole) on k(3) and dopamine synthesis capacity (DSC) determined by the four-parameter model and by the conventional tissue reference method. METHODS: Sixty-two individuals (31 patients and 31 control subjects) underwent F-18-DOPA positron emission tomography at baseline, and 15 patients were re-examined after 6 weeks. Clinical re-examinations were completed after 6 weeks (n = 28) and 6 months (n = 15). Symptoms were evaluated with the Positive and Negative Syndrome Scale. RESULTS: High baseline decarboxylation rates (k(3)) were associated with more positive symptoms at baseline (p , .001) and with symptom improvement after 6 weeks (p = .006). Subregion analyses showed that baseline k(3) for the putamen (p = .003) and nucleus accumbens (p = .013) and DSC values for the nucleus accumbens (p = .003) were associated with psychotic symptoms. The tissue reference method yielded no associations between DSC and symptoms or symptom improvement. Neither method revealed any effects of group or treatment on average magnitudes of k(3) or DSC, whereas changes in dopamine synthesis were correlated with higher baseline values, implying a potential effect of treatment. CONCLUSIONS: Striatal decarboxylation rate at baseline was associated with psychotic symptoms and treatment response. The strong association between k(3) and treatment effect potentially implicate on new treatment strategies.

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