Literature DB >> 28393354

Discrepancy in prevalence of Huntington's disease in two Swedish regions.

A-K Roos1, L Wiklund1, K Laurell1.   

Abstract

BACKGROUND: Huntington's disease (HD) is a neurodegenerative disease with an autosomal dominant pattern of inheritance. The prevalence varies between different geographical regions with an estimated average in Europe of about 6/100 000. Parts of northern Sweden are known to have an accumulation of HD, but no prevalence studies have been undertaken for 50 years. OBJECT: The aim of this study was to estimate the prevalence of HD in the two different Swedish counties of Jämtland and Uppsala and compare them with the reported prevalence in Europe.
METHOD: Patients registered with the diagnosis of HD were identified through medical records in each county. Presymptomatic patients were excluded. We also compared the annual number of individuals with HD registered in the database of the National Board of Health and Welfare in these regions, with all of Sweden.
RESULTS: The prevalence of HD was found to be 22.1/100 000 in Jämtland and 4.9/100 000 in Uppsala county. The mean age was 62.2 years and 61.8 years, respectively. The annual average of patients with HD registered at inpatient care was 1.5/100 000 in Jämtland, 0.44/100 000 in Uppsala county, and 0.56/100 000 in all of Sweden.
CONCLUSION: The prevalence of patients with the diagnosis of HD is four times higher in the county of Jämtland than in the county of Uppsala, where the prevalence is more similar to the average in Europe. Our results support earlier findings of regional variations of HD prevalence with an accumulation in certain parts of northern Sweden.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  cross-sectional study; epidemiology; huntington's disease; neurodegenerative disease; prevalence

Mesh:

Year:  2017        PMID: 28393354     DOI: 10.1111/ane.12762

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  4 in total

1.  HTT haplogroups in Finnish patients with Huntington disease.

Authors:  Susanna Ylönen; Jussi O T Sipilä; Marja Hietala; Kari Majamaa
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2.  Genetic epidemiological characteristics of a Hungarian subpopulation of patients with Huntington's disease.

Authors:  Katalin Despotov; Dénes Zádori; Gábor Veres; Katalin Jakab; Gabriella Gárdián; Eszter Tóth; Tamás Zsigmond Kincses; László Vécsei; András Ajtay; Dániel Bereczki; Péter Klivényi
Journal:  BMC Neurol       Date:  2021-02-18       Impact factor: 2.474

3.  High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study.

Authors:  Jimmy Sundblom; Valter Niemelä; Maria Ghazarian; Ann-Sofi Strand; Ingvar A Bergdahl; Jan-Håkan Jansson; Stefan Söderberg; Eva-Lena Stattin
Journal:  Sci Rep       Date:  2020-06-17       Impact factor: 4.996

4.  Huntington's disease among immigrant groups and Swedish-born individuals: a cohort study of all adults 18 years of age and older in Sweden.

Authors:  Per Wändell; Sten Fredrikson; Axel C Carlsson; Xinjun Li; Jan Sundquist; Kristina Sundquist
Journal:  Neurol Sci       Date:  2021-01-30       Impact factor: 3.307

  4 in total

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