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Case Reports
. 2015 Apr;28(2):126-32.
doi: 10.1177/1971400915581740. Epub 2015 May 11.

Brain MR diffusion tensor imaging in Kennedy's disease

Affiliations
Case Reports

Brain MR diffusion tensor imaging in Kennedy's disease

Francesco Garaci et al. Neuroradiol J. 2015 Apr.

Abstract

Introduction: Kennedy's disease (KD) is a progressive degenerative disorder affecting lower motor neurons. We investigated the correlation between disease severity and whole brain white matter microstructure, including upper motor neuron tracts, by using diffusion-tensor imaging (DTI) in eight patients with KD in whom disease severity was evaluated using the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS).

Methods: From DTI acquisitions we obtained maps of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (L1) and radial diffusivities (L2, L3). We then employed tract-based spatial statistics (TBSS) to investigate within-patient correlations of DTI invariants with ALSFRS and disease duration (DD).

Results: We found a significant correlation between low ALSFRS and 1) low FA values in association commissural and projection fibers, and 2) high L3 values in commissural tracts and fronto-parietal white matter. Additionally, we found a significant association between longer DD and 1) low FA in the genu and body of corpus callosum, association fibers and midbrain and 2) high L1 in projection and association tracts.

Conclusions: The associations between clinical variables and white matter microstructural changes in areas thought to be spared by the disease process support the hypothesis of a multisystem involvement in the complex pathogenic mechanisms responsible for the clinical disability of these patients.

Keywords: ALSFRS; DTI; Kennedy’s disease; TBSS; disease duration; fractional anisotropy; mean diffusivity.

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Figures

Figure 1.
Figure 1.
Results of voxel-based analysis of FA and L3 maps in patient group by using TBSS. Upper panel: Red shows regions where FA correlates significantly with ALSFRS score: in highlighted areas, FA is significantly lower (p < 0.05, TFCE) when ALFSRS is lower. Lower panel: Blue shows regions where L3 correlates significantly with ALSFRS score: in highlighted areas, L3 is significantly higher (p < 0.05, TFCE) when ALSFRS is lower. For each brain section Montreal Neurological Institute (MNI) coordinates are displayed. FA: fractional anisotropy; TBSS: tract-based spatial statistics; ALSFRS: Amyotrophic Lateral Sclerosis Functional Rating Scale; L3: radial diffusivity; TFCE: threshold-free cluster enhancement.
Figure 2.
Figure 2.
Results of voxel-based analysis of FA and L1 maps in patient group by using TBSS. Upper panel: Red shows regions where FA correlates significantly with disease duration in highlighted areas, FA is significantly lower (p < 0.05, TFCE) when disease duration is higher. Lower panel: Blue shows regions where L1 correlates significantly with disease duration in highlighted areas, L1 is significantly lower (p < 0.05, TFCE) when disease duration is higher. For each brain section Montreal Neurological Institute (MNI) coordinates are displayed. FA: fractional anisotropy; TBSS: tract-based spatial statistics; L1: axial diffusivity.

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References

    1. Katsuno M, Banno H, Suzuki K, et al. Clinical features and molecular mechanisms of spinal and bulbar muscular atrophy (SBMA). Adv Exp Med Biol 2010; 685: 64–74. - PubMed
    1. Harding AE, Thomas PK, Baraitser M, et al. X-linked recessive bulbospinal neuronopathy: A report of ten cases. J Neurol Neurosurg Psychiatry 1982; 45: 1012–1019. - PMC - PubMed
    1. Shaw PJ, Thagesen H, Tomkins J, et al. Kennedy’s disease: Unusual molecular pathologic and clinical features. Neurology 1998; 51: 252–255. - PubMed
    1. Karitzky J, Block W, Mellies JK, et al. Proton magnetic resonance spectroscopy in Kennedy syndrome. Arch Neurol 1999; 56: 1465–1471. - PubMed
    1. Mader I, Karitzky J, Klose U, et al. Proton MRS in Kennedy disease: Absolute metabolite and macromolecular concentrations. J Magn Reson Imaging 2002; 16: 160–167. - PubMed

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