Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Jun;34(6):858-865.
doi: 10.1002/mds.27653. Epub 2019 Mar 13.

Huntington's disease in the United States: Variation by demographic and socioeconomic factors

Affiliations

Huntington's disease in the United States: Variation by demographic and socioeconomic factors

Emilie Bruzelius et al. Mov Disord. 2019 Jun.

Abstract

Background: Despite extensive research regarding the etiology of Huntington's disease, relatively little is known about the epidemiology of this rare disorder, particularly in the United States where there are no national-scale estimates of the disease.

Objectives: To provide national-scale estimates of Huntington's disease in a U.S. population and to test whether disease rates are increasing, and whether frequency varies by race, ethnicity, or other factors.

Methods: Using an insurance database of over 67 million enrollees, we retrospectively identified a cohort of 3,707 individuals diagnosed with Huntington's disease between 2003 and 2016. We estimated annual incidence, annual diagnostic frequency, and tested for trends over time and differences in diagnostic frequency by sociodemographic characteristics.

Results: During the observation period, the age-adjusted cumulative incidence rate was1.22 per 100,000 persons (95% confidence interval: 1.53, 1.65), and age-adjusted diagnostic frequency was 6.52 per 100,000 persons (95% confidence interval: 5.31, 5.66); both rates remained relatively stable over the 14-year period. We identified several previously unreported differences in Huntington's disease frequency by self-reported sex, income, and race/ethnicity. However, racial/ethnic differences were of lower magnitude than have previously been reported in other country-level studies.

Conclusions: In these large-scale estimates of U.S. Huntington's disease epidemiology, we found stable disease frequency rates that varied by several sociodemographic factors. These findings suggest that disease patterns may be more driven by social or environmental factors than has previously been appreciated. Results further demonstrate the potential utility of administrative Big Data in rare disease epidemiology when other data sources are unavailable. © 2019 International Parkinson and Movement Disorder Society.

Keywords: Big Data; Huntington's disease; incidence and prevalence; neurodegenerative diseases; neuroepidemiology.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest: No conflicts to disclose

References

    1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group. Cell 1993; 72(6):971–83. - PubMed
    1. Duyao M, Ambrose C, Myers R, et al. Trinucleotide repeat length instability and age of onset in Huntington’s disease. Nat Genet 1993; 4(4):387–92. doi:10.1038/ng0893-387 - DOI - PubMed
    1. Genetic Modifiers of Huntington’s Disease C. Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease. Cell 2015; 162(3):516–26. doi:10.1016/j.cell.2015.07.003 - DOI - PMC - PubMed
    1. Gusella JF, MacDonald ME, Lee JM. Genetic modifiers of Huntington’s disease. Mov Disord 2014; 29(11):1359–65. doi:10.1002/mds.26001 - DOI - PubMed
    1. Sipila JO, Paivarinta M. Why We Still Need More Research on the Epidemiology of Huntington’s Disease. Neuroepidemiology 2016; 46(2):154–5. doi:10.1159/000444230 - DOI - PubMed

Publication types