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Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society)
INTRODUCTION: Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The pharmacological treatment of motor signs (e.g. chorea) may favorably or unfavorably impact other facets of the disease phenotype (such as mood and cognition...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652593/ https://www.ncbi.nlm.nih.gov/pubmed/37968732 http://dx.doi.org/10.1186/s42466-023-00285-1 |
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author | Saft, Carsten Burgunder, Jean-Marc Dose, Matthias Jung, Hans Heinrich Katzenschlager, Regina Priller, Josef Nguyen, Huu Phuc Reetz, Kathrin Reilmann, Ralf Seppi, Klaus Landwehrmeyer, Georg Bernhard |
author_facet | Saft, Carsten Burgunder, Jean-Marc Dose, Matthias Jung, Hans Heinrich Katzenschlager, Regina Priller, Josef Nguyen, Huu Phuc Reetz, Kathrin Reilmann, Ralf Seppi, Klaus Landwehrmeyer, Georg Bernhard |
author_sort | Saft, Carsten |
collection | PubMed |
description | INTRODUCTION: Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The pharmacological treatment of motor signs (e.g. chorea) may favorably or unfavorably impact other facets of the disease phenotype (such as mood and cognition). Similarly, pharmacotherapy for behavioral issues may modify the motor phenotype. Sometimes synergistic effects can be achieved. In patients undergoing pragmatic polypharmacological therapy, emerging complaints may stem from the employed medications' side effects, a possibility that needs to be considered. It is recommended to clearly and precisely delineate the targeted signs and symptoms (e.g., chorea, myoclonus, bradykinesia, Parkinsonism, or dystonia). Evidence from randomized controlled trials (RCTs) is limited. SUMMARY OR DEFINITION OF THE TOPIC: Therefore, the guidelines prepared for the German Neurological Society (DGN) for German-speaking countries intentionally extend beyond evidence from RCTs and aim to synthesize evidence from RCTs and recommendations of experienced clinicians. RECOMMENDATIONS: First-line treatment for chorea is critically discussed, and a preference in prescription practice for using tiapride instead of tetrabenazine is noted. In severe chorea, combining two antidopaminergic drugs with a postsynaptic (e.g., tiapride) and presynaptic mode of action (e.g., tetrabenazine) is discussed as a potentially helpful strategy. Sedative side effects of both classes of compounds can be used to improve sleep if the highest dosage of the day is given at night. Risperidone, in some cases, may ameliorate irritability but also chorea and sleep disorders. Olanzapine can be helpful in the treatment of weight loss and chorea, and quetiapine as a mood stabilizer with an antidepressant effect. CONCLUSIONS: Since most HD patients simultaneously suffer from distinct motor signs and distinct psychiatric/behavioral symptoms, treatment should be individually adapted. |
format | Online Article Text |
id | pubmed-10652593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106525932023-11-16 Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) Saft, Carsten Burgunder, Jean-Marc Dose, Matthias Jung, Hans Heinrich Katzenschlager, Regina Priller, Josef Nguyen, Huu Phuc Reetz, Kathrin Reilmann, Ralf Seppi, Klaus Landwehrmeyer, Georg Bernhard Neurol Res Pract Guidelines INTRODUCTION: Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The pharmacological treatment of motor signs (e.g. chorea) may favorably or unfavorably impact other facets of the disease phenotype (such as mood and cognition). Similarly, pharmacotherapy for behavioral issues may modify the motor phenotype. Sometimes synergistic effects can be achieved. In patients undergoing pragmatic polypharmacological therapy, emerging complaints may stem from the employed medications' side effects, a possibility that needs to be considered. It is recommended to clearly and precisely delineate the targeted signs and symptoms (e.g., chorea, myoclonus, bradykinesia, Parkinsonism, or dystonia). Evidence from randomized controlled trials (RCTs) is limited. SUMMARY OR DEFINITION OF THE TOPIC: Therefore, the guidelines prepared for the German Neurological Society (DGN) for German-speaking countries intentionally extend beyond evidence from RCTs and aim to synthesize evidence from RCTs and recommendations of experienced clinicians. RECOMMENDATIONS: First-line treatment for chorea is critically discussed, and a preference in prescription practice for using tiapride instead of tetrabenazine is noted. In severe chorea, combining two antidopaminergic drugs with a postsynaptic (e.g., tiapride) and presynaptic mode of action (e.g., tetrabenazine) is discussed as a potentially helpful strategy. Sedative side effects of both classes of compounds can be used to improve sleep if the highest dosage of the day is given at night. Risperidone, in some cases, may ameliorate irritability but also chorea and sleep disorders. Olanzapine can be helpful in the treatment of weight loss and chorea, and quetiapine as a mood stabilizer with an antidepressant effect. CONCLUSIONS: Since most HD patients simultaneously suffer from distinct motor signs and distinct psychiatric/behavioral symptoms, treatment should be individually adapted. BioMed Central 2023-11-16 /pmc/articles/PMC10652593/ /pubmed/37968732 http://dx.doi.org/10.1186/s42466-023-00285-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Guidelines Saft, Carsten Burgunder, Jean-Marc Dose, Matthias Jung, Hans Heinrich Katzenschlager, Regina Priller, Josef Nguyen, Huu Phuc Reetz, Kathrin Reilmann, Ralf Seppi, Klaus Landwehrmeyer, Georg Bernhard Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title | Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title_full | Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title_fullStr | Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title_full_unstemmed | Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title_short | Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society) |
title_sort | symptomatic treatment options for huntington’s disease (guidelines of the german neurological society) |
topic | Guidelines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652593/ https://www.ncbi.nlm.nih.gov/pubmed/37968732 http://dx.doi.org/10.1186/s42466-023-00285-1 |
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