Brain atrophy in pure and complicated hereditary spastic paraparesis: A quantitative 3D MRI study

J. Kassubek*, A. D. Sperfeld, A. Baumgartner, H. J. Huppertz, A. Riecker, F. D. Juengling

*Corresponding author for this work
21 Citations (Scopus)

Abstract

Hereditary spastic paraparesis (HSP) is a heterogeneous group of neurodegenerative disorders with progressive lower limb spasticity, categorized into pure (p-HSP) and complicated forms (c-HSP). The purpose of this study was to evaluate if brain volumes in HSP were altered compared with a control population. Brain volumes were determined in patients suffering from HSP, including both p-HSP (n = 21) and c-HSP type (n = 12), and 30 age-matched healthy controls, using brain parenchymal fractions (BPF) calculated from 3D MRI data in an observer-independent procedure. In addition, the tissue segments of grey and white matter were analysed separately. In HSP patients, BPF were significantly reduced compared with controls both for the whole patient group (P < 0.001) and for both subgroups, indicating considerable brain atrophy. In contrast to controls who showed a decline of brain volumes with age, this physiological phenomenon was less pronounced in HSP. Therefore, global brain parenchyma reduction, involving both grey and white matter, seems to be a feature in both subtypes of HSP. Atrophy was more pronounced in c-HSP, consistent with the more severe phenotype including extramotor involvement. Thus, global brain atrophy, detected by MRI-based brain volume quantification, is a biological marker in HSP subtypes.

Original languageEnglish
JournalEuropean Journal of Neurology
Volume13
Issue number8
Pages (from-to)880-886
Number of pages7
ISSN1351-5101
DOIs
Publication statusPublished - 08.2006

Research Areas and Centers

  • Health Sciences

DFG Research Classification Scheme

  • 206-07 Clinical Neurology Neurosurgery and Neuroradiology
  • 206-08 Cognitive and Systemic Human Neuroscience

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