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

Author:

Ludolph Albert CORCID,Emilian Susanne,Dreyhaupt Jens,Rosenbohm Angela,Kraskov Alexander,Lemon Roger N,Del Tredici KellyORCID,Braak HeikoORCID

Abstract

ObjectiveA 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.MethodsIn 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).ResultsThe 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.ConclusionsThese 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.

Funder

Virtual Helmholtz Institute for RNA Dysmetabolism in ALS and FTD

German Research Council

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

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