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Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment

In Huntington's disease (HD), the main clinical symptoms include depression, apathy, cognitive deficits, motor deficiencies and involuntary movements. Cognitive, mood and behavioral changes may precede motor symptoms by up to 15 years. The treatment of these diverse symptoms is challenging. Tet...

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Autores principales: Molnar, Maria Judit, Molnar, Viktor, Fedor, Mariann, Csehi, Reka, Acsai, Karoly, Borsos, Beata, Grosz, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866559/
https://www.ncbi.nlm.nih.gov/pubmed/35222108
http://dx.doi.org/10.3389/fpsyt.2021.825532
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author Molnar, Maria Judit
Molnar, Viktor
Fedor, Mariann
Csehi, Reka
Acsai, Karoly
Borsos, Beata
Grosz, Zoltan
author_facet Molnar, Maria Judit
Molnar, Viktor
Fedor, Mariann
Csehi, Reka
Acsai, Karoly
Borsos, Beata
Grosz, Zoltan
author_sort Molnar, Maria Judit
collection PubMed
description In Huntington's disease (HD), the main clinical symptoms include depression, apathy, cognitive deficits, motor deficiencies and involuntary movements. Cognitive, mood and behavioral changes may precede motor symptoms by up to 15 years. The treatment of these diverse symptoms is challenging. Tetrabenazine and deutetrabenazine are the only medications specifically approved for Huntington's chorea, but they do not affect the non-motor symptoms. For these, antidepressants, antipsychotics, and benzodiazepines have demonstrated benefit in some cases and can be used off-label. These drugs, due to sedative side effects, may negatively influence cognition. Sixteen patients having HD received a 12-week off-label cariprazine (CAR) treatment (1.5–3 mg/day). Cognitive performance and behavioral changes were measured by the Addenbrooke Cognitive Examination (ACE) test, the Cognitive and Behavioral part of the Unified Huntington's Disease Rating Scale (UHDRS), and the Beck Depression Inventory (BDI). Mixed model for repeated measures was fitted to the data, with terms of visit, baseline (BL) and their interaction. Cariprazine treatment resulted in the following changes from BL to week 12, respectively: the mean score of BDI decreased from 17.7 ± 10.7 to 10.0 ± 10.7 (p <0.0097), while the Behavioral Assessment score of the UHDRS decreased from 54.9 ± 11.3 to 32.5 ± 15.4 (p < 0.0001); ACE score increased from 75.1 ± 11.0 to 89.0 ± 9.3 (p < 0.0001); Cognitive Verbal Fluency score from 6.2 ± 2.5 to 7.7 ± 2.7 (p < 0.0103); Symbol Digit Test from 9.2 ± 6.9 to 12.3 ± 8.9 (p < 0.0009). Mild akathisia was the most frequent side effect, presenting in 2 out of 16 patients (12.5%). We conclude that CAR had a positive effect on depressive mood, apathy and cognitive functions in patients with early stage of HD. Based on the neurobiological basis of these symptoms, CAR can improve the dopamine imbalance of the prefrontal cortex. This draws attention to the transdiagnostic approach which supports the further understanding of the similar symptomatology of different neuropsychiatric disorders and helps to identify new indications of pharmaceutical compounds.
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spelling pubmed-88665592022-02-25 Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment Molnar, Maria Judit Molnar, Viktor Fedor, Mariann Csehi, Reka Acsai, Karoly Borsos, Beata Grosz, Zoltan Front Psychiatry Psychiatry In Huntington's disease (HD), the main clinical symptoms include depression, apathy, cognitive deficits, motor deficiencies and involuntary movements. Cognitive, mood and behavioral changes may precede motor symptoms by up to 15 years. The treatment of these diverse symptoms is challenging. Tetrabenazine and deutetrabenazine are the only medications specifically approved for Huntington's chorea, but they do not affect the non-motor symptoms. For these, antidepressants, antipsychotics, and benzodiazepines have demonstrated benefit in some cases and can be used off-label. These drugs, due to sedative side effects, may negatively influence cognition. Sixteen patients having HD received a 12-week off-label cariprazine (CAR) treatment (1.5–3 mg/day). Cognitive performance and behavioral changes were measured by the Addenbrooke Cognitive Examination (ACE) test, the Cognitive and Behavioral part of the Unified Huntington's Disease Rating Scale (UHDRS), and the Beck Depression Inventory (BDI). Mixed model for repeated measures was fitted to the data, with terms of visit, baseline (BL) and their interaction. Cariprazine treatment resulted in the following changes from BL to week 12, respectively: the mean score of BDI decreased from 17.7 ± 10.7 to 10.0 ± 10.7 (p <0.0097), while the Behavioral Assessment score of the UHDRS decreased from 54.9 ± 11.3 to 32.5 ± 15.4 (p < 0.0001); ACE score increased from 75.1 ± 11.0 to 89.0 ± 9.3 (p < 0.0001); Cognitive Verbal Fluency score from 6.2 ± 2.5 to 7.7 ± 2.7 (p < 0.0103); Symbol Digit Test from 9.2 ± 6.9 to 12.3 ± 8.9 (p < 0.0009). Mild akathisia was the most frequent side effect, presenting in 2 out of 16 patients (12.5%). We conclude that CAR had a positive effect on depressive mood, apathy and cognitive functions in patients with early stage of HD. Based on the neurobiological basis of these symptoms, CAR can improve the dopamine imbalance of the prefrontal cortex. This draws attention to the transdiagnostic approach which supports the further understanding of the similar symptomatology of different neuropsychiatric disorders and helps to identify new indications of pharmaceutical compounds. Frontiers Media S.A. 2022-02-10 /pmc/articles/PMC8866559/ /pubmed/35222108 http://dx.doi.org/10.3389/fpsyt.2021.825532 Text en Copyright © 2022 Molnar, Molnar, Fedor, Csehi, Acsai, Borsos and Grosz. https://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 Psychiatry
Molnar, Maria Judit
Molnar, Viktor
Fedor, Mariann
Csehi, Reka
Acsai, Karoly
Borsos, Beata
Grosz, Zoltan
Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title_full Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title_fullStr Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title_full_unstemmed Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title_short Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
title_sort improving mood and cognitive symptoms in huntington's disease with cariprazine treatment
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866559/
https://www.ncbi.nlm.nih.gov/pubmed/35222108
http://dx.doi.org/10.3389/fpsyt.2021.825532
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