The influence of gender on phenotype and disease progression in patients with Huntington's disease

Daniel Zielonka, Johan Marinus, Raymund A C Roos, Giuseppe De Michele, Stefano Di Donato, Hein Putter, Jerzy Marcinkowski, Ferdinando Squitieri, Anna Rita Bentivoglio, G. Bernhard Landwehrmeyer

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. The aim of this study is to determine whether gender plays a role in the phenotypic expression and progression of HD. Methods: 1267 patients with HD (636 women) from the Registry project of the EHDN were included. A cross-sectional analysis (ANCOVA) controlling for differences in age at onset, disease burden, disease duration, smoking status, alcohol abuse, depression and the number of years of education, was performed to evaluate if there were differences between men and women in UHDRS motor, function and cognitive scores. Additionally, analyses on follow-up data using linear mixed models with the same covariates were performed to test for gender-related differences in progression. Results: Baseline features did not differ between genders, with the exception of a higher frequency of past and current depression among women, and a higher number of years of education as well as more frequent alcohol abuse and smoking among men. In the cross-sectional ANCOVA analyses of patients with a mid-age HD onset, women showed worse scores than men in the functional domain (TFC, P = 0.001; UHDRS functional, P = 0.033), UHDRS motor (P = 0.033). The longitudinal analyses showed a faster rate of progression in women in the functional assessment (P = 0.025), the motor assessment (P = 0.032) and the independence scale (P = 0.008). Conclusions: These results suggest a complex gender effect on the phenotypical presentation and the rate of disease progression in HD, with slightly more severe phenotype and faster rate of progression in women in especially the motor and functional domains.

Original languageEnglish
Pages (from-to)192-197
Number of pages6
JournalParkinsonism and Related Disorders
Volume19
Issue number2
DOIs
Publication statusPublished - Feb 2013

Keywords

  • CAG repeats
  • Gender
  • Huntington's disease
  • Progression
  • UHDRS

ASJC Scopus subject areas

  • Geriatrics and Gerontology
  • Clinical Neurology
  • Neurology

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