Huntington's Disease

351 Users are discussing this topic

PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Huntington's Disease written for patients

Huntington's disease (HD) is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and dystonia, inco-ordination, cognitive decline and behavioural difficulties.[1] It is associated with cell loss within the basal ganglia and cortex. Huntington's disease was first described by George Huntington in 1872. The disease is associated with increases in the length of a cysteine-adenosine-guanine (CAG) triplet repeat present in a gene called 'huntingtin' (HTT) located on chromosome 4p16.3.[2] There are many symptomatic treatments but no therapies that alter disease progression.[3] 

  • The prevalence is estimated at between 1 in 10,000 and 1 in 20,000.
  • HD is the most common hereditary neurodegenerative disorder.[5] It is the most common genetic cause of chorea.[6] 
  • The mean age at onset of symptoms is 30-50 years.
  • In some cases symptoms start before the age of 20 years with behavioural disturbances and learning difficulties at school  - juvenile Huntington's disease (JHD); this is more common when the condition has been inherited from the father.[2] 

NEW - log your activity

  • Notes
    Add notes to any clinical page and create a reflective diary
  • Track
    Automatically track and log every page you have viewed
  • Print
    Print and export a summary to use in your appraisal
Click to find out more »

Typically, onset of symptoms is in middle age but the disorder can manifest at any age.[1]There is often a prodromal phase of mild psychotic and behavioural symptoms before the development of chorea. Clinical and neuroradiological abnormalities can be demonstrated in gene-positive individuals before the onset of manifest HD, even as far as 15 years before the disease onset.[7]

  • Early signs may be personality change, self-neglect, apathy with clumsiness, fidgeting with fleeting facial grimaces.
  • Behavioural problems may lead to family conflict, marital breakdown and job loss before a formal diagnosis has been made.
  • Depressed mood is significantly higher in HD gene carriers than in the general population and in individuals with HD it has been reported to be as common as 69%.[5] 
  • HD then leads to progressive chorea, rigidity and dementia. It is frequently associated with seizures.
  • Chorea is initially mild but may be severe and cause uncontrollable limb movements.
  • As the disease progresses, chorea is gradually replaced by dystonia and Parkinsonian features.
  • Dysarthria, dysphagia and abnormal eye movements are common. There may also be other movement disorders - eg, tics and myoclonus.
  • HD patients can develop a wide array of dysfunction, including HD-related cardiomyopathy and skeletal muscle wasting.[5] 

HD is associated with increasing depression, bradykinesia, cognitive impairment and aggression as the disease progresses.[8]Behavioural difficulties include apathy or lack of initiative, dysphoria, irritability, agitation or anxiety, poor self-care, poor judgment and inflexibility.[1]Late features include spasticity, clonus, supranuclear gaze palsy and extensor plantar responses. The rate of cognitive decline is very variable.

JHD (6% of all cases of HD) is defined as an age of onset of younger than 20 years. It causes Parkinsonian features, dystonia, pyramidal tract signs, dementia and epilepsy. Chorea is often mild and may be absent.

  • Neuroacanthocytosis: a group of genetic conditions that are characterised by movement disorders and acanthocytosis (abnormally-shaped red blood cells).
  • Tardive dyskinesia and other causes of chorea.
  • Other causes of dementia.
  • MRI and CT scans in moderate-to-severe HD show a loss of striatal volume and increased size of the frontal horns of the lateral ventricles; however, scans are usually unhelpful for diagnosis of early disorder.[1]
  • If genetic testing is considered then extensive genetic counselling in a specialised unit is required in view of the implications of an untreatable, familial, progressive, neurodegenerative disease.
  • Testing for alternative causes of movement disorders (including systemic lupus erythematosus (SLE), antiphospholipid antibody syndrome, thyroid disease and Wilson's disease) and dementia.
  • Genetic testing is available at regional genetics clinics (contact details are available in the linked Huntington's Disease Association information sheet).
  • The clinics follow an agreed genetic counselling procedure which is usually spread over at least three sessions to help the person decide whether or not to go ahead with the test.
  • Two separate blood samples are taken to double-check the results. The affected parent's blood may also be tested to check the original diagnosis of HD.
  • One section of the Huntington's gene contains cytosine, adenine and guanine repeated a number of times. In the faulty gene there are many repetitions.
  • Four types of results are recognised:[5] 
    • Under 27 repetitions is unequivocally normal.
    • Between 27-35 repetitions is normal but there is a small chance that the repeat may increase in future generations.
    • Between 36-39 repetitions is abnormal but there is a chance the person may be affected very late in life or even not at all.
    • Over 40 repetitions is unequivocally abnormal.
  • Although the test can tell whether the person is carrying the HD mutation, it cannot tell when the disease itself will start to develop.
  • Current drug therapy has no effect on the progression of disability.
  • Hyperkinesias and psychiatric symptoms may respond well to pharmacotherapy but neuropsychological deficits and dementia remain untreatable.[10]
  • Standards of care:
    • Patients, their families and carers require a great deal of physical and emotional support.
    • The care of someone with HD is complex and involves many specialties including neurology, general practice, psychiatry, speech and language therapy, physiotherapy, clinical genetics, neuropsychology and dietetics, as well as social work and palliative care. However, there is little research on this aspect of HD.
    • The European Huntington's Disease Network has created 'Standards of Care' which are expected to benefit patients directly, as well as encourage collection of data to contribute towards research into its cause and prevention.[11] 
  • Chorea:
    • Benzodiazepines, valproic acid, dopamine-depleting agents (eg, tetrabenazine) and neuroleptics may be useful.
    • A Cochrane review found that no intervention proved to have consistent symptomatic control in HD. Tetrabenazine was considered to be the antichoreic drug with the best-quality data available.[12] 
    • An algorithm for the drug treatment of chorea has been developed from international expert opinion.[5] 
    • Pridopidine is a new drug thought to act as a possible 'dopaminergic stabiliser'. It is the subject of a phase II clinical research study.[5] 
  • Patients with predominant bradykinesia and rigidity may benefit from levodopa or dopamine agonists.
  • Depression:[5]
    • Needs prompt recognition and treatment.
    • Selective serotonin reuptake inhibitors (SSRIs) are first-choice antidepressants. Refractory depression may require ECT treatment.
    • The risk of suicide ranges from 5-10%; it is highest initially when the patient recognises the first symptoms of HD; the second 'danger period' occurs as independence starts to be lost.
  • Psychosis:
    • Antipsychotic medications may be necessary. Newer atypical antipsychotics are preferable in view of their lower incidence of extrapyramidal side-effects.
    • Antipsychotics may also be needed in the treatment of obsessive-compulsive behaviours and irritability when psychotherapy and behavioural management strategies have proved inadequate.[5] 
  • Neural and stem cell transplantation have been studied in humans but only in small studies.
  • Deep brain stimulation is a new approach for palliative treatment of choreatic movements, dystonia and stiffness.

Predictive genetic testing allows for early identification of HD carriers and observational studies are increasing knowledge of the pathophysiology and natural progression of HD. In addition the development of sensitive measurements that allow earlier diagnosis are expected to provide the ideal time for the use of disease-modifying therapy, such as gene silencing.[13] 

  • This is currently a relentlessly progressive, neurodegenerative disorder. The clinical features develop steadily with severe increase in choreic movements and dementia.
  • Death is usually from an intercurrent illness - eg, pneumonia.
  • Suicide is the second most common cause of death.[4] 

Further reading & references

  1. Walker FO; Huntington's disease. Lancet. 2007 Jan 20;369(9557):218-28.
  2. Huntington Disease, HD; Online Mendelian Inheritance in Man (OMIM)
  3. Mestre T, Ferreira J, Coelho MM, et al; Therapeutic interventions for disease progression in Huntington's disease. Cochrane Database Syst Rev. 2009 Jul 8;(3):CD006455.
  4. Roos RA; Huntington's disease: a clinical review. Orphanet J Rare Dis. 2010 Dec 20;5(1):40. doi: 10.1186/1750-1172-5-40.
  5. Zielonka D, Mielcarek M, Landwehrmeyer GB; Update on Huntington's disease: advances in care and emerging therapeutic options. Parkinsonism Relat Disord. 2015 Mar;21(3):169-78. doi: 10.1016/j.parkreldis.2014.12.013. Epub 2014 Dec 19.
  6. Cardoso F; Huntington disease and other choreas. Neurol Clin. 2009 Aug;27(3):719-36, vi.
  7. Ha AD, Fung VS; Huntington's disease. Curr Opin Neurol. 2012 Aug;25(4):491-8. doi: 10.1097/WCO.0b013e3283550c97.
  8. Singer C; Comprehensive treatment of Huntington disease and other choreic disorders. Cleve Clin J Med. 2012 Jul;79 Suppl 2:S30-4. doi: 10.3949/ccjm.79.s2a.06.
  9. Predictive Testing for Huntington’s Disease; Huntington’s Disease Association
  10. Bonelli RM, Hofmann P; A systematic review of the treatment studies in Huntington's disease since 1990. Expert Opin Pharmacother. 2007 Feb;8(2):141-53.
  11. Rae D, Hamilton A, Miedzybrodzka Z; A Standard of Care in Huntington's Disease, European Huntington's Disease Network (EHDN) Standards of Care Working Group, 2013
  12. Mestre T, Ferreira J, Coelho MM, et al; Therapeutic interventions for symptomatic treatment in Huntington's disease. Cochrane Database Syst Rev. 2009 Jul 8;(3):CD006456.
  13. Tang C, Feigin A; Monitoring Huntington's disease progression through preclinical and early stages. Neurodegener Dis Manag. 2012 Aug 1;2(4):421-435.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Colin Tidy
Current Version:
Peer Reviewer:
Dr Adrian Bonsall
Document ID:
2278 (v25)
Last Checked:
05/05/2016
Next Review:
04/05/2021

Did you find this health information useful?

Yes No

Thank you for your feedback!

Subcribe to the Patient newsletter for healthcare and news updates.

We would love to hear your feedback!

 
 
Patient Access app - find out more Patient facebook page - Like our page