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
. 2007 Nov;78(11):1209-12.
doi: 10.1136/jnnp.2006.112532. Epub 2007 Mar 1.

Widespread white matter changes in Kennedy disease: a voxel based morphometry study

Affiliations

Widespread white matter changes in Kennedy disease: a voxel based morphometry study

Jan Kassubek et al. J Neurol Neurosurg Psychiatry. 2007 Nov.

Abstract

Objective: X linked spinobulbar muscular atrophy (Kennedy disease (KD)), which is clinically characterised mainly by neuromuscular and endocrine symptoms, has to be considered as a multisystem disorder. Based on clinical evidence of central nervous system involvement, potential KD associated cerebral volume alterations were analysed in vivo.

Methods: Whole brain based analysis of optimised voxel based morphometry (VBM) was applied to three dimensional MRI data from 18 genetically confirmed KD patients and compared with age matched controls.

Results: Subtle decreases in grey matter volume, mainly localised in frontal areas, were found, but extensive white matter atrophy was observed, particularly in frontal areas, but also involving multiple additional subcortical areas, the cerebellar white matter and the dorsal brainstem from the midbrain to the medulla oblongata.

Conclusion: The VBM results demonstrated a morphological correlate of central nervous system involvement in KD, in agreement with aspects of the clinical phenotype (behavioural abnormalities, central-peripheral axonopathy) and with pathohistological findings.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None.

Similar articles

Cited by

References

    1. La Spada A R, Roling D B, Harding A E.et al Meiotic stability and genotype–phenotype correlation of the trinucleotide repeat in X‐linked spinal and bulbar muscular atrophy. Nat Genet 19922301–304. - PubMed
    1. Sperfeld A D, Karitzky J, Brummer D.et al X‐linked bulbospinal neuronopathy: Kennedy disease. Arch Neurol 2002591921–1926. - PubMed
    1. Buecking A, Pfister R. Sensory ataxia as the initial clinical symptom in X‐linked recessive bulbospinal neuronopathy. J Neurol Neurosurg Psychiatry 200069277 - PMC - PubMed
    1. Guidetti D, Vescovini E, Motti L.et al X‐linked bulbar and spinal muscular atrophy or Kennedy disease: clinical, neurophysiological, neuropathological, neuropsychological and molecular study of a large family. J Neurol Sci 1996135140–148. - PubMed
    1. Good C D, Johnsrude I S, Ashburner J.et al A voxel‐based morphometric study of ageing in 465 normal adult human brains. Neuroimage 20011421–36. - PubMed