Neuropsychiatric aspects of Huntington's disease

التفاصيل البيبلوغرافية
العنوان: Neuropsychiatric aspects of Huntington's disease
المؤلفون: J. M. Hamilton, Jeffrey L. Cummings, Michael S. Mega, Rebecca E. Ready, Jane S. Paulsen
المصدر: Journal of Neurology, Neurosurgery & Psychiatry. 71:310-314
بيانات النشر: BMJ, 2001.
سنة النشر: 2001
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Psychomotor agitation, Neurocognitive Disorders, Disease, Neuropsychological Tests, Neuropsychiatry, Irritability, Severity of Illness Index, Cognition, Huntington's disease, mental disorders, Prevalence, medicine, Humans, Dementia, Apathy, Psychiatry, Psychomotor Agitation, Aged, Visual Cortex, Chorea, Middle Aged, medicine.disease, Frontal Lobe, Psychiatry and Mental health, Huntington Disease, Motor Skills, Papers, Educational Status, Female, Surgery, Neurology (clinical), Nervous System Diseases, medicine.symptom, Mental Status Schedule, Psychology
الوصف: OBJECTIVE Neuropsychiatric symptoms are common in Huntington9s disease and have been considered its presenting manifestation. Research characterising these symptoms in Huntington9s disease is variable, however, encumbered by limitations within and across studies. Gaining a better understanding of neuropsychiatric symptoms is essential, as these symptoms have implications for disease management, prognosis, and quality of life for patients and caregivers. METHOD Fifty two patients with Huntington9s disease were administered standardised measures of cognition, psychiatric symptoms, and motor abnormalities. Patient caregivers were administered the neuropsychiatric inventory. RESULTS Ninety eight per cent of the patients exhibited neuropsychiatric symptoms, the most prevalent being dysphoria, agitation, irritability, apathy, and anxiety. Symptoms ranged from mild to severe and were unrelated to dementia and chorea. CONCLUSIONS Neuropsychiatric symptoms are prevalent in Huntington9s disease and are relatively independent of cognitive and motor aspects of the disease. Hypothesised links between neuropsychiatric symptoms of Huntington9s disease and frontal-striatal circuitry were explored. Findings indicate that dimensional measures of neuropsychiatric symptoms are essential to capture the full range of pathology in Huntington9s disease and are vital to include in a comprehensive assessment of the disease.
تدمد: 0022-3050
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::144ac6485b1cb0b701e4cfeef1c03103Test
https://doi.org/10.1136/jnnp.71.3.310Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....144ac6485b1cb0b701e4cfeef1c03103
قاعدة البيانات: OpenAIRE