33 - References
References
834 The Maudsley® Prescribing Guidelines in Psychiatry CHAPTER 10 Cognitive symptoms Cognitive disturbances may emerge many years before motor disturbances.7 The progression of cognitive decline is gradual25 and dementia is inevitable in late stages. Although a wide variety of agents have been studied,2,11 none has become established treatment and the benefit of most remains unclear.26 There is insufficient evidence to support the use of acetylcholinesterase inhibitors27 and no evidence to support any other medications to treat dementia in HD.11,28 References
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- Jellinger KA. The pathobiology of depression in Huntington’s disease: an unresolved puzzle. J Neural Transm 2024; doi: 10.1007/ s00702-024-02750-w.
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- Oosterloo M, et al. Obsessive-compulsive and perseverative behaviors in Huntington’s disease. J Huntingtons Dis 2019; 8:1–7.
- Karagas NE, et al. Irritability in Huntington’s disease. J Huntingtons Dis 2020; 9:107–113.
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- Connolly A, et al. Meta-analysis and systematic review of vesicular monoamine transporter (VMAT-2) inhibitors in schizophrenia and psychosis. Psychopharmacology (Berl) 2024; 241:225–241.
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- Van der Vaart T, et al. Treatment of cognitive deficits in genetic disorders: a systematic review of clinical trials of diet and drug treatments. JAMA Neurol 2015; 72:1052–1060.
- Li Y, et al. Cholinesterase inhibitors for rarer dementias associated with neurological conditions. Cochrane Database Syst Rev 2015; 3:CD009444.
- O’Brien JT, et al. Clinical practice with anti-dementia drugs: a revised (third) consensus statement from the British Association for Psychopharmacology. J Psychopharmacol 2017; 31:147–168.
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