Literature DB >> 32665323

Pattern of paresis in ALS is consistent with the physiology of the corticomotoneuronal projections to different muscle groups.

Albert C Ludolph1,2, Susanne Emilian3, Jens Dreyhaupt4, Angela Rosenbohm3, Alexander Kraskov5, Roger N Lemon6, Kelly Del Tredici7, Heiko Braak7.   

Abstract

OBJECTIVE: A recent neuroanatomical staging scheme of amyotrophic lateral sclerosis (ALS) indicates that a cortical lesion may spread, as a network disorder, both at the cortical level and via corticofugal tracts, including corticospinal projections providing direct monosynaptic input to α-motoneurons. These projections are involved preferentially and early in ALS. If these findings are clinically relevant, the pattern of paresis in ALS should primarily involve those muscle groups that receive the strongest direct corticomotoneuronal (CM) innervation.
METHODS: In a large cohort (N=436), we analysed retrospectively the pattern of muscle paresis in patients with ALS using the UK Medical Research Council (MRC) scoring system; we subsequently carried out two independent prospective studies in two smaller groups (N=92 and N=54).
RESULTS: The results indicated that a characteristic pattern of paresis exists. When pairs of muscle groups were compared within patients, the group known to receive the more pronounced CM connections was significantly weaker. Within patients, there was greater relative weakness (lower MRC score) in thumb abductors versus elbow extensors, for hand extensors versus hand flexors and for elbow flexors versus elbow extensors. In the lower limb, knee flexors were relatively weaker than extensors, and plantar extensors were weaker than plantar flexors.
CONCLUSIONS: These findings were mostly significant (p<0.01) for all six pairs of muscles tested and provide indirect support for the concept that ALS may specifically affect muscle groups with strong CM connections. This specific pattern could help to refine clinical and electrophysiological ALS diagnostic criteria and complement prospective clinicopathological correlation studies. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  amyotrophic lateral sclerosis; corticospinal tract; monosynaptic transmission; neuropathological staging; primates

Year:  2020        PMID: 32665323     DOI: 10.1136/jnnp-2020-323331

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  7 in total

Review 1.  The Dying Forward Hypothesis of ALS: Tracing Its History.

Authors:  Andrew Eisen
Journal:  Brain Sci       Date:  2021-02-27

2.  The split-elbow index: A biomarker of the split elbow sign in ALS.

Authors:  Nathan Pavey; Mana Higashihara; Mehdi A J van den Bos; Parvathi Menon; Steve Vucic
Journal:  Clin Neurophysiol Pract       Date:  2021-12-09

Review 3.  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

4.  Case Report: A 72-Year-Old Woman With Progressive Motor Weakness, Dry Eyes and High Levels of Serum Neurofilament Light Chain.

Authors:  Maria Janina Wendebourg; Jens Kuhle; Martin Hardmeier
Journal:  Front Neurol       Date:  2022-07-11       Impact factor: 4.086

Review 5.  The Cortical "Upper Motoneuron" in Health and Disease.

Authors:  Roger N Lemon
Journal:  Brain Sci       Date:  2021-05-12

Review 6.  Corticospinal vs Rubrospinal Revisited: An Evolutionary Perspective for Sensorimotor Integration.

Authors:  Rafael Olivares-Moreno; Paola Rodriguez-Moreno; Veronica Lopez-Virgen; Martín Macías; Moisés Altamira-Camacho; Gerardo Rojas-Piloni
Journal:  Front Neurosci       Date:  2021-06-11       Impact factor: 4.677

7.  Progressive arm muscle weakness in ALS follows the same sequence regardless of onset site: use of TOMS, a novel analytic method to track limb strength.

Authors:  Nimish J Thakore; Brian J Drawert; Brittany R Lapin; Erik P Pioro
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2021-02-23       Impact factor: 3.528

  7 in total

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