Literature DB >> 21512742

White matter involvement in idiopathic normal pressure hydrocephalus: a voxel-based diffusion tensor imaging study.

Shigenori Kanno1, Nobuhito Abe, Makoto Saito, Masahito Takagi, Yoshiyuki Nishio, Akiko Hayashi, Makoto Uchiyama, Risa Hanaki, Hirokazu Kikuchi, Kotaro Hiraoka, Hiroshi Yamasaki, Osamu Iizuka, Atsushi Takeda, Yasuto Itoyama, Shoki Takahashi, Etsuro Mori.   

Abstract

The aim of this study was to characterise the white matter damage involved in idiopathic normal pressure hydrocephalus (INPH) using diffusion tensor imaging (DTI) and the relationship between this damage and clinical presentation. Twenty patients with INPH, 20 patients with Alzheimer's disease and 20 patients with idiopathic Parkinson's disease (as disease control groups) were enrolled in this study. Mean diffusivity (MD) and fractional anisotropy (FA) were determined using DTI, and these measures were analysed to compare the INPH group with the control groups and with certain clinical correlates. On average, the supratentorial white matter presented higher MD and lower FA in the INPH group than in the control groups. In the INPH group, the mean hemispheric FA correlated with some of the clinical measures, whereas the mean hemispheric MD did not. On a voxel-based statistical map, white matter involvement with high MD was localised to the periventricular regions, and white matter involvement with low FA was localised to the corpus callosum and the subcortical regions. The total scores on the Frontal Assessment Battery were correlated with the FA in the frontal and parietal subcortical white matter, and an index of gait disturbance was correlated with the FA in the anterior limb of the left internal capsule and under the left supplementary motor area. DTI revealed the presence of white matter involvement in INPH. Whereas white matter regions with high MD were not related to symptom manifestation, those with low FA were related to motor and cognitive dysfunction in INPH.

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Year:  2011        PMID: 21512742     DOI: 10.1007/s00415-011-6038-5

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


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