Can a single muscle have both its Upper Motor Neuron (UMN) and Lower Motor Neuron (LMN) damaged?

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Last updated: February 20, 2025View editorial policy

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From the Guidelines

Yes, it is possible for a single muscle to have both its upper and lower motor neurons damaged, as seen in conditions like amyotrophic lateral sclerosis (ALS) where both upper and lower motor neurons degenerate, potentially affecting the same muscle. This can occur in conditions that affect multiple levels of the nervous system simultaneously. For example, in ALS, both upper and lower motor neurons degenerate, potentially affecting the same muscle, as noted in a study published in the Journal of the American College of Radiology in 2020 1.

When this happens, the muscle would exhibit signs of both upper and lower motor neuron damage:

  • Upper motor neuron damage: Increased muscle tone, hyperreflexia, and spasticity
  • Lower motor neuron damage: Muscle weakness, atrophy, and fasciculations The combination of these effects can lead to a mixed clinical picture, with the muscle showing signs of both flaccid and spastic paralysis. This dual damage severely impairs muscle function and control, as patients with ALS typically present with hypertonicity and hyperreflexia (upper motor neuron degeneration) and muscle fasciculations, weakness, and atrophy (lower motor neuron degeneration) 1.

Understanding this possibility is crucial for accurate diagnosis and appropriate management of neurological conditions affecting motor function. It highlights the importance of comprehensive neurological examinations to assess both upper and lower motor neuron integrity when evaluating muscle weakness or paralysis. Electromyography and nerve conduction velocity are key tests in diagnosing conditions like ALS, with imaging relied upon mainly to exclude other conditions with similar clinical presentations rather than confirm or facilitate the diagnosis of ALS 1.

From the Research

Upper and Lower Motor Neuron Damage

  • A single muscle can have both its Upper Motor Neuron (UMN) and Lower Motor Neuron (LMN) damaged, as seen in diseases such as amyotrophic lateral sclerosis (ALS) 2, 3, 4.
  • In ALS, both UMN and LMN are involved in the process of neurodegeneration, leading to progressive muscle wasting and clinical heterogeneity of the disease 4.
  • Studies have shown that muscles in tetraplegic patients can have both UMN and LMN lesions, with the majority of forearm muscles retaining some or all of their LMN intact 5.
  • The involvement of both UMN and LMN can impact disease prognosis and overall survival in ALS patients, highlighting the importance of evaluating the severity of both UMN and LMN involvement in disease diagnosis and staging 4.

Clinical Implications

  • The assessment of UMN involvement remains essentially clinical, with biomarkers of pathological UMN involvement required to ensure timely access to therapeutic trials 2.
  • Motor unit firing rate and variability can be useful variables in assessing UMN involvement in motor system disorders, with decreased physiological modulation of LMN firing rate seen in patients with lower limb spasticity 3.
  • Exercise therapy can be beneficial for patients with muscle diseases, but may have a blunted response in motor neuron diseases, with high-intensity training showing promise as a safe and effective exercise method 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Assessment of the upper motor neuron in amyotrophic lateral sclerosis.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2016

Research

Motor unit firing in amyotrophic lateral sclerosis and other upper and lower motor neurone disorders.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2012

Research

Exercise therapy for muscle and lower motor neuron diseases.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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