-
- Steve Vucic and Matthew C Kiernan.
- Prince of Wales Medical Research Institute, Barker Street, Randwick, Sydney, NSW 2031, Australia.
- Clin Neurophysiol. 2008 May 1; 119 (5): 1088-96.
ObjectiveSpinobulbomuscular atrophy, or Kennedy's disease (KD), is an X-linked inherited neurodegenerative disorder that clinically may "mimic" amyotrophic lateral sclerosis (ALS). Although KD is regarded as a pure lower motor neuron disorder, recent studies have reported on the presence of corticomotoneuron dysfunction in KD, similar to ALS. To clarify these discordant findings, the present study applied novel threshold tracking transcranial magnetic stimulation (TMS) techniques to gain further insights into corticomotoneuron function and thereby possible pathophysiological processes underlying neurodegeneration in KD.MethodsCortical excitability studies were undertaken in 7 KD patients, 55 normal controls, 45 ALS patients and 6 patients with the flail arm variant ALS (FAV), a pure lower motor neuron form of ALS. Motor evoked responses were recorded over abductor pollicis brevis.ResultsShort-interval intracortical inhibition (SICI) in KD was similar to controls (KD 6.0+/-1.2%; controls 8.4+/-1.1%, P=0.08), but significantly greater when compared to ALS and FAV patients (ALS 0.7+/-0.7%; FAV -0.8+/-0.7%, P<0.0001). The magnetic stimulus-response curve gradient, motor evoked potential amplitude and cortical silent period duration in KD patients were similar to controls. In ALS and FAV patients, the magnetic stimulus-response curve gradient (ALS and FAV, P<0.01) and motor evoked potential amplitude (ALS and FAV, P<0.05) were significantly increased, while the cortical silent period duration was reduced (ALS, P<0.001) when compared to KD patients.ConclusionsThreshold tracking TMS techniques have established normal corticomotoneuron function in KD, clearly differentiating KD from ALS.SignificanceThe present study has established normal cortical excitability in KD, inferring a lack of significant cortical involvement in this disease.
Notes
Knowledge, pearl, summary or comment to share?You can also include formatting, links, images and footnotes in your notes
- Simple formatting can be added to notes, such as
*italics*
,_underline_
or**bold**
. - Superscript can be denoted by
<sup>text</sup>
and subscript<sub>text</sub>
. - Numbered or bulleted lists can be created using either numbered lines
1. 2. 3.
, hyphens-
or asterisks*
. - Links can be included with:
[my link to pubmed](http://pubmed.com)
- Images can be included with:
![alt text](https://bestmedicaljournal.com/study_graph.jpg "Image Title Text")
- For footnotes use
[^1](This is a footnote.)
inline. - Or use an inline reference
[^1]
to refer to a longer footnote elseweher in the document[^1]: This is a long footnote.
.