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Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients

Patients with chronic schizophrenia often display enlarged striatal volumes, and antipsychotic drugs may contribute via the dopamine D(2/3) receptor (D(2/3)R) blockade. Separating the effects of disease from medication is challenging due to the lack of a proper placebo-group. To address this, we con...

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Autores principales: Andersen, Helle G., Raghava, Jayachandra M., Svarer, Claus, Wulff, Sanne, Johansen, Louise B., Antonsen, Patrick K., Nielsen, Mette Ø., Rostrup, Egill, Vernon, Anthony C., Jensen, Lars T., Pinborg, Lars H., Glenthøj, Birte Y., Ebdrup, Bjørn H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251943/
https://www.ncbi.nlm.nih.gov/pubmed/32508577
http://dx.doi.org/10.3389/fnins.2020.00484
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author Andersen, Helle G.
Raghava, Jayachandra M.
Svarer, Claus
Wulff, Sanne
Johansen, Louise B.
Antonsen, Patrick K.
Nielsen, Mette Ø.
Rostrup, Egill
Vernon, Anthony C.
Jensen, Lars T.
Pinborg, Lars H.
Glenthøj, Birte Y.
Ebdrup, Bjørn H.
author_facet Andersen, Helle G.
Raghava, Jayachandra M.
Svarer, Claus
Wulff, Sanne
Johansen, Louise B.
Antonsen, Patrick K.
Nielsen, Mette Ø.
Rostrup, Egill
Vernon, Anthony C.
Jensen, Lars T.
Pinborg, Lars H.
Glenthøj, Birte Y.
Ebdrup, Bjørn H.
author_sort Andersen, Helle G.
collection PubMed
description Patients with chronic schizophrenia often display enlarged striatal volumes, and antipsychotic drugs may contribute via the dopamine D(2/3) receptor (D(2/3)R) blockade. Separating the effects of disease from medication is challenging due to the lack of a proper placebo-group. To address this, we conducted a longitudinal study of antipsychotic-naïve, first-episode schizophrenia patients to test the hypothesis that selective blockade of D(2/3)R would induce a dose-dependent striatal volume increase. Twenty-one patients underwent structural magnetic resonance imaging (sMRI), single-photon emission computed tomography (SPECT), and symptom severity ratings before and after six weeks of amisulpride treatment. Twenty-three matched healthy controls underwent sMRI and baseline SPECT. Data were analyzed using repeated measures and multiple regression analyses. Correlations between symptom severity decrease, volume changes, dose and receptor occupancy were explored. Striatal volumes did not differ between patients and controls at baseline or follow-up, but a significant group-by-time interaction was found (p = 0.01). This interaction was explained by a significant striatal volume increase of 2.1% in patients (Cohens d = 0.45). Striatal increase was predicted by amisulpride dose, but not by either D(2/3)R occupancy or baseline symptom severity. A significant reduction in symptom severity was observed at a mean dose of 233.3 (SD = 109.9) mg, corresponding to D(2/3)R occupancy of 44.65%. Reduction in positive symptoms correlated significantly with striatal volume increase, driven by reductions in hallucinations. Our data demonstrate a clear link between antipsychotic treatment and striatal volume increase in antipsychotic-naïve schizophrenia patients. Moreover, the treatment-induced striatal volume increase appears clinically relevant by correlating to reductions in core symptoms of schizophrenia.
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spelling pubmed-72519432020-06-05 Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients Andersen, Helle G. Raghava, Jayachandra M. Svarer, Claus Wulff, Sanne Johansen, Louise B. Antonsen, Patrick K. Nielsen, Mette Ø. Rostrup, Egill Vernon, Anthony C. Jensen, Lars T. Pinborg, Lars H. Glenthøj, Birte Y. Ebdrup, Bjørn H. Front Neurosci Neuroscience Patients with chronic schizophrenia often display enlarged striatal volumes, and antipsychotic drugs may contribute via the dopamine D(2/3) receptor (D(2/3)R) blockade. Separating the effects of disease from medication is challenging due to the lack of a proper placebo-group. To address this, we conducted a longitudinal study of antipsychotic-naïve, first-episode schizophrenia patients to test the hypothesis that selective blockade of D(2/3)R would induce a dose-dependent striatal volume increase. Twenty-one patients underwent structural magnetic resonance imaging (sMRI), single-photon emission computed tomography (SPECT), and symptom severity ratings before and after six weeks of amisulpride treatment. Twenty-three matched healthy controls underwent sMRI and baseline SPECT. Data were analyzed using repeated measures and multiple regression analyses. Correlations between symptom severity decrease, volume changes, dose and receptor occupancy were explored. Striatal volumes did not differ between patients and controls at baseline or follow-up, but a significant group-by-time interaction was found (p = 0.01). This interaction was explained by a significant striatal volume increase of 2.1% in patients (Cohens d = 0.45). Striatal increase was predicted by amisulpride dose, but not by either D(2/3)R occupancy or baseline symptom severity. A significant reduction in symptom severity was observed at a mean dose of 233.3 (SD = 109.9) mg, corresponding to D(2/3)R occupancy of 44.65%. Reduction in positive symptoms correlated significantly with striatal volume increase, driven by reductions in hallucinations. Our data demonstrate a clear link between antipsychotic treatment and striatal volume increase in antipsychotic-naïve schizophrenia patients. Moreover, the treatment-induced striatal volume increase appears clinically relevant by correlating to reductions in core symptoms of schizophrenia. Frontiers Media S.A. 2020-05-20 /pmc/articles/PMC7251943/ /pubmed/32508577 http://dx.doi.org/10.3389/fnins.2020.00484 Text en Copyright © 2020 Andersen, Raghava, Svarer, Wulff, Johansen, Antonsen, Nielsen, Rostrup, Vernon, Jensen, Pinborg, Glenthøj and Ebdrup. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Andersen, Helle G.
Raghava, Jayachandra M.
Svarer, Claus
Wulff, Sanne
Johansen, Louise B.
Antonsen, Patrick K.
Nielsen, Mette Ø.
Rostrup, Egill
Vernon, Anthony C.
Jensen, Lars T.
Pinborg, Lars H.
Glenthøj, Birte Y.
Ebdrup, Bjørn H.
Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title_full Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title_fullStr Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title_full_unstemmed Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title_short Striatal Volume Increase After Six Weeks of Selective Dopamine D(2/3) Receptor Blockade in First-Episode, Antipsychotic-Naïve Schizophrenia Patients
title_sort striatal volume increase after six weeks of selective dopamine d(2/3) receptor blockade in first-episode, antipsychotic-naïve schizophrenia patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251943/
https://www.ncbi.nlm.nih.gov/pubmed/32508577
http://dx.doi.org/10.3389/fnins.2020.00484
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