Literature DB >> 11464937

Functional magnetic resonance imaging (fMRI) clinical studies in ALS--paradigms, problems and promises.

B R Brooks1, K Bushara, A Khan, J Hershberger, J O Wheat, D Belden, H Henningsen.   

Abstract

Functional magnetic resonance imaging (fMRI) provides high-resolution, non-invasive estimates of neural activity detected by a blood oxygen level dependent signal by assessing the increase in blood flow to the local vasculature that accompanies neural activity in the brain. fMRI studies with standard hand motor test (index-thumb opposition, ITO, or pinch) in ALS patients show good test-retest reliability and similar amplitude of signals in ALS patients compared with control subjects. Isometric force can be performed with careful control for the force exerted, recruitment of other muscles and motion artefact. The volume (number of voxels above threshold) of sensorimotor and cerebellar cortex activated by ITO is reproducibly larger in ALS patients compared with control subjects. Imagined movements in ALS have been studied, as in amputees, and larger volumes are activated in ALS patients with imagined movements as well, compared with control subjects. fMRI studies in ALS patients evaluating cortical activation during pure somatosensory stimulation cutaneous stimulation of the hand to elicit the palmomental response and cutaneous stimulation of the sole to elicit the plantar response - indicate that ALS patients activate a significantly smaller volume of the contralateral sensorimotor cortex compared to control subjects. No statistically significant difference was seen in other areas, including the ipsilateral cerebellum and the contralateral thalamus. An anterior shift in the volume of cortex activated by these paradigms occurs in ALS patients, with a volume of activation, anteriorly, not activated in control subjects. fMRI studies will complement other clinical neurophysiological and neuroimaging techniques in our future attempts to solve the riddle of ALS and other motor neuron diseases.

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Year:  2000        PMID: 11464937     DOI: 10.1080/14660820052415790

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord        ISSN: 1466-0822


  10 in total

Review 1.  Neuroimaging in amyotrophic lateral sclerosis.

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Journal:  Neurotherapeutics       Date:  2011-01       Impact factor: 7.620

2.  Potential impact of a 32-channel receiving head coil technology on the results of a functional MRI paradigm.

Authors:  J Albrecht; M Burke; K Haegler; V Schöpf; A M Kleemann; M Paolini; M Wiesmann; J Linn
Journal:  Clin Neuroradiol       Date:  2010-09-21       Impact factor: 3.649

3.  Longitudinal monitoring of motor neuron circuitry in FALS rats using in-vivo phMRI.

Authors:  Ji-Kyung Choi; Alpaslan Dedeoglu; Bruce G Jenkins
Journal:  Neuroreport       Date:  2010-02-17       Impact factor: 1.837

4.  Subcortical reorganization in amyotrophic lateral sclerosis.

Authors:  C Konrad; A Jansen; H Henningsen; J Sommer; P A Turski; B R Brooks; S Knecht
Journal:  Exp Brain Res       Date:  2006-03-25       Impact factor: 1.972

5.  Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging.

Authors:  G Caiazzo; D Corbo; F Trojsi; G Piccirillo; M Cirillo; M R Monsurrò; F Esposito; Gioacchino Tedeschi
Journal:  J Neurol       Date:  2013-10-15       Impact factor: 4.849

6.  Noninvasive detection of brainstem and spinal cord axonal degeneration in an amyotrophic lateral sclerosis mouse model.

Authors:  Joong Hee Kim; Tzy-Haw Wu; Matthew D Budde; Jin-Moo Lee; Sheng-Kwei Song
Journal:  NMR Biomed       Date:  2010-12-08       Impact factor: 4.044

Review 7.  Amyotrophic lateral sclerosis: objective upper motor neuron markers.

Authors:  Petra Kaufmann; Hiroshi Mitsumoto
Journal:  Curr Neurol Neurosci Rep       Date:  2002-01       Impact factor: 5.081

Review 8.  Corticostriatal connectivity and its role in disease.

Authors:  Gordon M G Shepherd
Journal:  Nat Rev Neurosci       Date:  2013-04       Impact factor: 34.870

Review 9.  The strength of corticomotoneuronal drive underlies ALS split phenotypes and reflects early upper motor neuron dysfunction.

Authors:  Andrew Eisen; Peter Bede
Journal:  Brain Behav       Date:  2021-10-28       Impact factor: 2.708

10.  Magnetic resonance imaging in amyotrophic lateral sclerosis.

Authors:  Katja Kollewe; Sonja Körner; Reinhard Dengler; Susanne Petri; Bahram Mohammadi
Journal:  Neurol Res Int       Date:  2012-07-09
  10 in total

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