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Review
doi: 10.1007/s40265-016-0670-4.

Current Pharmacological Approaches to Reduce Chorea in Huntington's Disease

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Review

Current Pharmacological Approaches to Reduce Chorea in Huntington's Disease

Emma M Coppen et al. Drugs.2017 Jan.

Abstract

There are currently no effective pharmacological agents available to stop or prevent the progression of Huntington's disease (HD), a rare hereditary neurodegenerative disorder. In addition to psychiatric symptoms and cognitive impairments, HD causes progressive motor disturbances, in particular choreiform movements, which are characterized by unwanted contractions of the facial muscles, trunk and extremities. Management of choreiform movements is usually advised if chorea interferes with daily functioning, causes social isolation, gait instability, falls, or physical injury. Although drugs to reduce chorea are available, only few randomized controlled studies have assessed the efficacy of these drugs, resulting in a high variety of prescribed drugs in clinical practice. The current pharmacological treatment options to reduce chorea in HD are outlined in this review, including the latest results on deutetrabenazine, a newly developed pharmacological agent similar to tetrabenazine, but with suggested less peak dose side effects. A review of the existing literature was conducted using the PubMed, Cochrane and Medline databases. In conclusion, mainly tetrabenazine, tiapride (in European countries), olanzapine, and risperidone are the preferred first choice drugs to reduce chorea among HD experts. In the existing literature, these drugs also show a beneficial effect on motor symptom severity and improvement of psychiatric symptoms. Generally, it is recommended to start with a low dose and increase the dose with close monitoring of any adverse effects. New interesting agents, such as deutetrabenazine and pridopidine, are currently under development and more randomized controlled trials are warranted to assess the efficacy on chorea severity in HD.

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Conflict of interest statement

Compliance with Ethical Standards Funding None. Conflict of interest EM Coppen has no conflicts of interest to declare. R. A. C. Roos received research grants from the CHDI Foundation, Gossweiler Foundation, and Teva Pharmaceutical Industries, Ltd.

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References

    1. Roos RAC. Huntington’s disease: a clinical review. Orphanet J Rare Dis. 2010;5:40. doi: 10.1186/1750-1172-5-40. - DOI - PMC - PubMed
    1. Mestre T, Ferreira J, Coelho MM, Rosa M, Sampaio C. Therapeutic interventions for symptomatic treatment in Huntington’s disease. Cochrane Database Syst Rev. 2009;(3):CD006456. doi:10.1002/14651858.CD006456.pub2. - PubMed
    1. Jankovic J, Roos RAC. Chorea associated with Huntington’s disease: to treat or not to treat? Mov Disord. 2014;29:1414–1418. doi: 10.1002/mds.25996. - DOI - PubMed
    1. The Huntington’s Disease Collaborative Research Group A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell. 1993;72:971–983. doi: 10.1016/0092-8674(93)90585-E. - DOI - PubMed
    1. De la Monte S, Vonsattel J, Richardson E. Morphometric demonstration of atrophic changes in cerebral cortex, white matter and neostriatum in Huntington’s disease. J Neuropathol Exp Neurol. 1988;47:516–525. doi: 10.1097/00005072-198809000-00003. - DOI - PubMed

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