Literature DB >> 22133668

Huntington's disease: current epidemiology and pharmacological management in UK primary care.

Catherine Sackley1, Thomas J Hoppitt, Melanie Calvert, Paramjit Gill, Benjamin Eaton, Guiqing Yao, Hardev Pall.   

Abstract

BACKGROUND: Recent debate suggests Huntington's disease (HD) may be more prevalent than previously reported. In addition, relatively little is known about current disease management. This study aims to provide epidemiological data and describe the pharmacological management of HD in the United Kingdom.
METHODS: A primary care research database was accessed to identify incident and prevalent HD cases between January 1, 2004, and December 31, 2008. Patients with Read codes denoting a definite diagnosis or possible diagnosis, and undiagnosed patients with a positive family history were identified. A subset of patients with a definite diagnosis and prescribed medication indicating symptom onset was also identified. Epidemiological data were estimated. Pharmacological prescriptions to HD patients from 2004 to 2008 were identified, and prescription frequencies were grouped according to the British National Formulary categories.
RESULTS: HD incidence estimates ranged from 0.44 to 0.78 per 100,000 person-years, and HD prevalence ranged from 5.96 to 6.54 per 100,000 of the population. Forty-four percent of pharmacological prescriptions targeted the central nervous system. Nearly half of the HD patients were prescribed antidepressants, and over 40% were prescribed analgesics.
CONCLUSIONS: Although prevalence estimates fell short of figures suggested in recent debate, it is feasible that the true prevalence may be much higher than previously reported. Pharmacological management appears to rely heavily on central nervous system drugs and nutrition support. Many of these drugs are prescribed to HD patients for reasons other than the medication's primary use. Further work is required to evaluate the impact of alternative management strategies, such as therapist intervention, counselling, and organisation support, on the patients' quality of life.
Copyright © 2011 S. Karger AG, Basel.

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Year:  2011        PMID: 22133668     DOI: 10.1159/000331912

Source DB:  PubMed          Journal:  Neuroepidemiology        ISSN: 0251-5350            Impact factor:   3.282


  7 in total

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3.  A Tale of Two Maladies? Pathogenesis of Depression with and without the Huntington's Disease Gene Mutation.

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4.  Natural history and burden of Huntington's disease in the UK: A population-based cohort study.

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Review 5.  Incidence of adult Huntington's disease in the UK: a UK-based primary care study and a systematic review.

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6.  The known burden of Huntington disease in the North of Scotland: prevalence of manifest and identified pre-symptomatic gene expansion carriers in the molecular era.

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7.  Prevalence of adult Huntington's disease in the UK based on diagnoses recorded in general practice records.

Authors:  Stephen J W Evans; Ian Douglas; Michael D Rawlins; Nancy S Wexler; Sarah J Tabrizi; Liam Smeeth
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-03-12       Impact factor: 10.154

  7 in total

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