Evidence map›Paper›PMID 35313602›Full record

ArticleClinical neurophysiology practice2022

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

Open access · goldAbstract read
In one paragraph

Article in Clinical neurophysiology practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Atsuko TsuneyamaDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Kazumoto ShibuyaDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Sonoko MisawaDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Yo-Ichi SuzukiDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Tomoki SuichiDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Yuta KojimaDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Keigo NakamuraDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Hiroki KanoDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Mario J PradoDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Satoshi KuwabaraDepartment of Neurology, Graduate School of Medicine, Chiba University Chiba, Japan.
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Activity-dependent hyperpolarization and conduction blockChronic inflammatory demyelinating polyneuropathyFatigueSpinal and bulbar muscular atrophy

Identifiers

PMID35313602
PMCPMC8933635
OpenAlexW4214912354

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.