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Published on: November 21, 2013
[Psychiatric symptoms of Huntington's disease]
Alzbeta Mühlbäck1,2, Rainer Hoffmann3, Nicolo Gabriele Pozzi3,4
1Huntington-Zentrum-Süd, kbo-Isar-Amper-Klinikum, Region München, Taufkirchen (Vils), Deutschland. Alzbeta.muehlbaeck@mri.tum.de.
Insights
Huntington's disease (HD) is an inherited disorder causing motor, cognitive, and psychiatric issues. This review covers HD's psychiatric symptoms, diagnosis, and current treatment options.
Area of Science:
- Neurology
- Genetics
- Psychiatry
Background:
- Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder.
- It manifests with a triad of motor, cognitive, and psychiatric symptoms.
- Psychiatric symptoms often precede motor deficits and significantly impact quality of life.
Purpose of the Study:
- To provide a comprehensive overview of the psychiatric manifestations in Huntington's disease.
- To discuss diagnostic approaches for HD-related psychiatric symptoms.
- To review current pharmacological and non-pharmacological treatment strategies.
Main Methods:
- Literature review of existing studies and clinical guidelines.
- Synthesis of information on diagnostic criteria and genetic testing for HD.
- Analysis of established treatment modalities for psychiatric symptoms in HD.
Main Results:
- Psychiatric symptoms in HD are diverse, including apathy, depression, anxiety, OCD, psychosis, and aggression.
- Diagnosis is confirmed by genetic testing for expanded CAG repeats in the Huntingtin gene.
- Current treatments focus on symptom management, as disease-modifying therapies are under investigation.
Conclusions:
- Psychiatric symptoms are a core feature of Huntington's disease, requiring careful management.
- Established clinical practice relies on expert opinion and experience from treating similar symptoms in other conditions.
- Further research into disease-modifying treatments for HD is crucial.
Abstract:
Huntington's disease (HD) is an autosomal dominant inherited disease, which leads to motor, cognitive and psychiatric symptoms. The diagnosis can be confirmed by genetic testing for extended CAG repeats in the Huntingtin gene. Mental and behavioral symptoms are common in HD and can appear several years before the onset of motor symptoms. The psychiatric symptoms include apathy, depression, anxiety, obsessive-compulsive symptoms and, in some cases, psychoses and aggression. These are currently restricted to symptomatic treatment as disease-modifying treatment approaches are still under investigation. The current clinical practice is based on expert opinions as well as experience with the treatment of similar symptoms in other neurological and mental health diseases. This article provides an overview of the complex psychiatric manifestations of HD, the diagnostic options and the established pharmacological and nonpharmacological treatment approaches.
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