Literature DB >> 21195663

Axonal integrity of corticospinal projections to the upper limbs in patients with pure hereditary spastic paraplegia.

Nicolas Lang1, Tim Optenhoefel, Guenther Deuschl, Stephan Klebe.   

Abstract

OBJECTIVE: Patients with hereditary spastic paraplegia (HSP) show pathological findings when transcranial magnetic stimulation (TMS) is used to test corticospinal projections to the lower limbs. However, TMS studies on the pathways to the upper limbs revealed inconsistent results. Standard clinical TMS procedures are not well suited for testing axonal integrity, which is thought to be affected in HSP. More appropriate measures can be achieved by testing corticospinal projections with the triple stimulation technique (TST).
METHODS: TST was used to test axonal integrity of corticospinal projections to the upper limbs in 15 patients with pure HSP (13 of whom were tested positive for SPG 4) and 15 healthy control subjects.
RESULTS: TST measurements revealed normal values for corticospinal transmission in all 15 patients with pure HSP, as well as in all healthy control subjects. No differences between groups could be found.
CONCLUSIONS: Axonal integrity of projections to the upper limbs is unimpaired in patients with pure HSP. The pathological mechanisms leading to spasticity and motor disability seem to be restricted to those fibres of the corticospinal pathways projecting to the lower limbs. SIGNIFICANCE: Abnormal corticospinal function to the upper limbs seems to be incompatible with pure HSP.
Copyright © 2010 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 21195663     DOI: 10.1016/j.clinph.2010.12.033

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  7 in total

Review 1.  Cellular pathways of hereditary spastic paraplegia.

Authors:  Craig Blackstone
Journal:  Annu Rev Neurosci       Date:  2012-04-20       Impact factor: 12.449

2.  Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4.

Authors:  Federica Ginanneschi; Maria A Carluccio; Andrea Mignarri; Alessandra Tessa; Filippo M Santorelli; Alessandro Rossi; Antonio Federico; Maria T Dotti
Journal:  Neurol Sci       Date:  2014-03-20       Impact factor: 3.307

3.  Motor Evoked Potentials in Hereditary Spastic Paraplegia-A Systematic Review.

Authors:  Sue-Faye Siow; Ruaridh Cameron Smail; Karl Ng; Kishore R Kumar; Carolyn M Sue
Journal:  Front Neurol       Date:  2019-09-18       Impact factor: 4.003

4.  Spinal direct current stimulation (tsDCS) in hereditary spastic paraplegias (HSP): A sham-controlled crossover study.

Authors:  Gianluca Ardolino; Tommaso Bocci; Martina Nigro; Maurizio Vergari; Alessio Di Fonzo; Sara Bonato; Filippo Cogiamanian; Francesca Cortese; Ilaria Cova; Sergio Barbieri; Alberto Priori
Journal:  J Spinal Cord Med       Date:  2018-12-03       Impact factor: 1.985

5.  Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Authors:  Gerald Pfeffer; Gráinne S Gorman; Helen Griffin; Marzena Kurzawa-Akanbi; Emma L Blakely; Ian Wilson; Kamil Sitarz; David Moore; Julie L Murphy; Charlotte L Alston; Angela Pyle; Jon Coxhead; Brendan Payne; George H Gorrie; Cheryl Longman; Marios Hadjivassiliou; John McConville; David Dick; Ibrahim Imam; David Hilton; Fiona Norwood; Mark R Baker; Stephan R Jaiser; Patrick Yu-Wai-Man; Michael Farrell; Allan McCarthy; Timothy Lynch; Robert McFarland; Andrew M Schaefer; Douglass M Turnbull; Rita Horvath; Robert W Taylor; Patrick F Chinnery
Journal:  Brain       Date:  2014-04-10       Impact factor: 13.501

6.  Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).

Authors:  Kathrin N Karle; Rebecca Schüle; Stephan Klebe; Susanne Otto; Christian Frischholz; Inga Liepelt-Scarfone; Ludger Schöls
Journal:  Orphanet J Rare Dis       Date:  2013-10-09       Impact factor: 4.123

7.  Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31.

Authors:  K M Fisher; P F Chinnery; S N Baker; M R Baker
Journal:  J Neurol       Date:  2013-11-13       Impact factor: 4.849

  7 in total

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