Fatigue and activity-dependent conduction block in neuromuscular disorders

Atsuko Tsuneyama; Kazumoto Shibuya; Sonoko Misawa; Yo-Ichi Suzuki; Tomoki Suichi; Yuta Kojima; Keigo Nakamura; Hiroki Kano; Mario J Prado; Satoshi Kuwabara

doi:10.1016/j.cnp.2022.02.003

Fatigue and activity-dependent conduction block in neuromuscular disorders

Clin Neurophysiol Pract. 2022 Mar 2:7:71-77. doi: 10.1016/j.cnp.2022.02.003. eCollection 2022.

Authors

Affiliation

¹ Department of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.

Abstract

Objective: Fatigue is a major disabling problem in patients with neuromuscular disorders. Both nerve demyelination and increased axonal branching associated with collateral sprouting reduce the safety factor for impulse transmission and could cause activity-dependent hyperpolarization and conduction block during voluntary contraction, and thus fatigue. This study aimed to investigate whether activity-dependent conduction block is associated with fatigue in demyelinating neuropathies and lower motor neuron disorders.

Methods: This study included 31 patients (17 with chronic inflammatory demyelinating polyneuropathy [CIDP] and 14 with spinal and bulbar muscular atrophy [SBMA]). Sixteen healthy subjects served as normal controls. Fatigue was assessed using the Fatigue Scale for Motor and Cognitive Functions (FSMC). Compound muscle action potential (CMAP) recording and nerve excitability testing after median nerve stimulation in the wrist were performed before and after maximal voluntary contraction of the abductor pollicis brevis for 1 min.

Results: Patients with CIDP/SBMA had prominent fatigue with higher FSMC motor scores (P < 0.0001) than normal controls. After voluntary contractions, CMAP amplitudes decreased significantly in four of the 17 patients with CIDP and one of the 14 patients with SBMA. The reduction in CMAP amplitude was associated with the fatigue score in the motor but not in the cognitive domain. After voluntary contraction, excitability testing showed axonal hyperpolarization in the normal and CIDP/SBMA groups.

Conclusions: In CIDP or SBMA, fatigue is caused by voluntary contraction-induced membrane hyperpolarization and conduction block, presumably due to the critically lowered safety factor due to demyelination or increased axonal branching.

Significance: Peripheral fatigue can be objectively assessed using CMAP amplitudes and nerve excitability testing.

Keywords: Activity-dependent hyperpolarization and conduction block; Chronic inflammatory demyelinating polyneuropathy; Fatigue; Spinal and bulbar muscular atrophy.