Literature DB >> 23899638

Estimated dopamine D₂ receptor occupancy and remission in schizophrenia: analysis of the CATIE data.

Sho Moriguchi1, Robert R Bies, Gary Remington, Takefumi Suzuki, David C Mamo, Koichiro Watanabe, Masaru Mimura, Bruce G Pollock, Hiroyuki Uchida.   

Abstract

In treating schizophrenia, 65% to 80% occupancy of dopamine D₂ receptors optimizes therapeutic efficacy while minimizing risks of extrapyramidal symptoms and cognitive impairments. However, it is unclear as to whether it is necessary to keep D₂ receptor occupancy within this therapeutic window to maintain clinical response. The data set from phase 1 of the Clinical Antipsychotic Trials in Intervention Effectiveness (CATIE) trial was reappraised. Thirty patients receiving risperidone (12 patients), olanzapine (12 patients), or ziprasidone (6 patients) fulfilled the following definition of remission and were included: a score of 3 or less on the 8 specific items in the Positive and Negative Syndrome Scale (ie, P1, P2, P3, N1, N4, N6, G5, and G9; adopted from Andreasen et al, 2005) at the initial assessment and months 1, 2, and 6. Peak and trough D₂ receptor occupancy levels at month 6 were estimated from plasma antipsychotic concentrations using population pharmacokinetic analysis and our D₂ prediction model. Estimated mean ± SD peak and trough D₂ receptor occupancy levels at month 6 were 70.3% ± 9.8% and 60.5% ± 20.2%, respectively; among these individuals, 46.7% (14 patients) did not achieve continuous blockade of 65% or greater (ie, trough D₂ occupancy of <65%). In conclusion, approximately half of patients with remission did not achieve continuous blockade of estimated D₂ receptor occupancy 5% or greater. These results extend our previous findings and suggest that sustained D₂ receptor occupancy greater than 65% may not always be necessary for the maintenance treatment of schizophrenia.

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Year:  2013        PMID: 23899638     DOI: 10.1097/JCP.0b013e3182979a0a

Source DB:  PubMed          Journal:  J Clin Psychopharmacol        ISSN: 0271-0749            Impact factor:   3.153


  6 in total

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Review 2.  Achieving the Lowest Effective Antipsychotic Dose for Patients with Remitted Psychosis: A Proposed Guided Dose-Reduction Algorithm.

Authors:  Chen-Chung Liu; Hiroyoshi Takeuchi
Journal:  CNS Drugs       Date:  2020-02       Impact factor: 5.749

3.  Tardive dyskinesia in relation to estimated dopamine D2 receptor occupancy in patients with schizophrenia: analysis of the CATIE data.

Authors:  Kazunari Yoshida; Robert R Bies; Takefumi Suzuki; Gary Remington; Bruce G Pollock; Yuya Mizuno; Masaru Mimura; Hiroyuki Uchida
Journal:  Schizophr Res       Date:  2014-02-01       Impact factor: 4.939

4.  Prediction of brain clozapine and norclozapine concentrations in humans from a scaled pharmacokinetic model for rat brain and plasma pharmacokinetics.

Authors:  Claire H Li; Robert E Stratford; Nieves Velez de Mendizabal; Thomas I F H Cremers; Bruce G Pollock; Benoit H Mulsant; Gary Remington; Robert R Bies
Journal:  J Transl Med       Date:  2014-08-20       Impact factor: 5.531

5.  Striatal Volume Increase After Six Weeks of Selective Dopamine D2/3 Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients.

Authors:  Helle G Andersen; Jayachandra M Raghava; Claus Svarer; Sanne Wulff; Louise B Johansen; Patrick K Antonsen; Mette Ø Nielsen; Egill Rostrup; Anthony C Vernon; Lars T Jensen; Lars H Pinborg; Birte Y Glenthøj; Bjørn H Ebdrup
Journal:  Front Neurosci       Date:  2020-05-20       Impact factor: 4.677

6.  Relationship between the timing of relapse and plasma drug levels following discontinuation of cariprazine treatment in patients with schizophrenia: indirect comparison with other second-generation antipsychotics after treatment discontinuation.

Authors:  Christoph U Correll; Rakesh Jain; Jonathan M Meyer; Antonia Periclou; Timothy Carrothers; Ágota Barabássy; Mehul Patel; Willie Earley
Journal:  Neuropsychiatr Dis Treat       Date:  2019-08-30       Impact factor: 2.570

  6 in total

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