Dopaminergic Activity in Antipsychotic-Naïve Patients Assessed With Positron Emission Tomography Before and After Partial Dopamine D 2 Receptor Agonist Treatment: Association With Psychotic Symptoms and Treatment Response

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-DOPA to F-dopamine (k ) and the effect of treatment on psychotic symptoms in antipsychotic-naïve patients w...

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Published in:Biological psychiatry (1969) Vol. 91; no. 2; p. 236
Main Authors: Sigvard, Anne Korning, Nielsen, Mette Ødegaard, Gjedde, Albert, Bojesen, Kirsten Borup, Fuglø, Dan, Tangmose, Karen, Kumakura, Yoshitaka, Heltø, Kim, Ebdrup, Bjørn H, Jensen, Lars Thorbjørn, Rostrup, Egill, Glenthøj, Birte Yding
Format: Journal Article
Language:English
Published: United States 15-01-2022
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Abstract 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-DOPA to F-dopamine (k ) and the effect of treatment on psychotic symptoms in antipsychotic-naïve patients with first-episode psychosis. We further explored the effect of treatment with a partial dopamine D receptor agonist (aripiprazole) on k and dopamine synthesis capacity (DSC) determined by the four-parameter model and by the conventional tissue reference method. Sixty-two individuals (31 patients and 31 control subjects) underwent F-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. High baseline decarboxylation rates (k ) 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 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 or DSC, whereas changes in dopamine synthesis were correlated with higher baseline values, implying a potential effect of treatment. Striatal decarboxylation rate at baseline was associated with psychotic symptoms and treatment response. The strong association between k and treatment effect potentially implicate on new treatment strategies.
AbstractList 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-DOPA to F-dopamine (k ) and the effect of treatment on psychotic symptoms in antipsychotic-naïve patients with first-episode psychosis. We further explored the effect of treatment with a partial dopamine D receptor agonist (aripiprazole) on k and dopamine synthesis capacity (DSC) determined by the four-parameter model and by the conventional tissue reference method. Sixty-two individuals (31 patients and 31 control subjects) underwent F-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. High baseline decarboxylation rates (k ) 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 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 or DSC, whereas changes in dopamine synthesis were correlated with higher baseline values, implying a potential effect of treatment. Striatal decarboxylation rate at baseline was associated with psychotic symptoms and treatment response. The strong association between k and treatment effect potentially implicate on new treatment strategies.
Author Tangmose, Karen
Kumakura, Yoshitaka
Gjedde, Albert
Ebdrup, Bjørn H
Rostrup, Egill
Bojesen, Kirsten Borup
Nielsen, Mette Ødegaard
Fuglø, Dan
Glenthøj, Birte Yding
Sigvard, Anne Korning
Heltø, Kim
Jensen, Lars Thorbjørn
Author_xml – sequence: 1
  givenname: Anne Korning
  surname: Sigvard
  fullname: Sigvard, Anne Korning
  email: anne.mette.sigvard@regionh.dk
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. Electronic address: anne.mette.sigvard@regionh.dk
– sequence: 2
  givenname: Mette Ødegaard
  surname: Nielsen
  fullname: Nielsen, Mette Ødegaard
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
– sequence: 3
  givenname: Albert
  surname: Gjedde
  fullname: Gjedde, Albert
  organization: Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Translational Neuropsychiatry Unit, Department of Clinical Medicine, University of Aarhus, Aarhus, Denmark
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  givenname: Kirsten Borup
  surname: Bojesen
  fullname: Bojesen, Kirsten Borup
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
– sequence: 5
  givenname: Dan
  surname: Fuglø
  fullname: Fuglø, Dan
  organization: Department of Nuclear Medicine, Herlev Hospital, University of Copenhagen, Herlev, Hovedstaden, Denmark
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  givenname: Karen
  surname: Tangmose
  fullname: Tangmose, Karen
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
– sequence: 7
  givenname: Yoshitaka
  surname: Kumakura
  fullname: Kumakura, Yoshitaka
  organization: Department of Diagnostic Radiology and Nuclear Medicine, Saitama Medical Center, Saitama Medical University, Saitama, Saitama Prefecture, Japan
– sequence: 8
  givenname: Kim
  surname: Heltø
  fullname: Heltø, Kim
  organization: Department of Anaesthesiology, Herlev Hospital, University of Copenhagen, Herlev, Hovedstaden, Denmark
– sequence: 9
  givenname: Bjørn H
  surname: Ebdrup
  fullname: Ebdrup, Bjørn H
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
– sequence: 10
  givenname: Lars Thorbjørn
  surname: Jensen
  fullname: Jensen, Lars Thorbjørn
  organization: Department of Nuclear Medicine, Herlev Hospital, University of Copenhagen, Herlev, Hovedstaden, Denmark
– sequence: 11
  givenname: Egill
  surname: Rostrup
  fullname: Rostrup, Egill
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
– sequence: 12
  givenname: Birte Yding
  surname: Glenthøj
  fullname: Glenthøj, Birte Yding
  organization: Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Center, Glostrup, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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Issue 2
Keywords Psychosis
Partial agonist
Striatum
Treatment outcome
Dopamine
Dopa decarboxylase
Aripiprazole
Antipsychotic-naïve schizophrenia
Positron emission tomography
F-DOPA
Language English
License Copyright © 2021 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.
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References 34916029 - Biol Psychiatry. 2022 Jan 15;91(2):170-172
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Snippet Dopamine activity has been associated with the response to antipsychotic treatment. Our study used a four-parameter model to test the association between the...
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StartPage 236
SubjectTerms Antipsychotic Agents - therapeutic use
Corpus Striatum
Dopamine
Dopamine Agonists - therapeutic use
Humans
Positron-Emission Tomography
Psychotic Disorders - diagnostic imaging
Psychotic Disorders - drug therapy
Title Dopaminergic Activity in Antipsychotic-Naïve Patients Assessed With Positron Emission Tomography Before and After Partial Dopamine D 2 Receptor Agonist Treatment: Association With Psychotic Symptoms and Treatment Response
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