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. 2022 Jan 7:7:27-33.
doi: 10.1016/j.cnp.2021.12.001. eCollection 2022.

The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy

Affiliations

The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy

Thomas Krøigård et al. Clin Neurophysiol Pract. .

Abstract

Objective: To explore potential differences in motor nerve excitability testing (NET) variables at group levels between patients with a clinical diagnosis of polyneuropathy (PNP), which did not fulfil diagnostic criteria of conventional nerve conduction studies (NCS) and patients without polyneuropathy. Such differences could support a role for NET in increasing the diagnostic sensitivity of NCS in chronic axonal PNP.

Methods: Motor NET was performed using the median nerve in patients with a clinical suspicion of PNP in addition to conventional NCS, skin biopsies, corneal confocal microscopy and structured clinical evaluation including scoring of neuropathy symptoms and signs.

Results: Of the 57 patients included, 32 had PNP, half of which had NCS, which fulfilled criteria for PNP (NCS+ PNP). There were no significant differences for any of the NET variables between PNP patients with non-diagnostic conventional NCS (NCS- PNP) and patients without PNP. Rheobase was increased, and Ted (undershoot) and subexcitability were decreased in NCS+ PNP. Sural amplitude, peroneal nerve F-wave latency and tibial nerve F-wave-latency were correlated with subexcitability, and tibial nerve motor amplitude was correlated with rheobase.

Conclusions: NET was correlated with conventional NCS and no differences were found between NCS- PNP patients and patients without PNP.

Significance: NET does not seem to offer any additional diagnostic value in chronic mixed etiology neuropathy.

Keywords: Diagnosis; Nerve conduction studies; Nerve excitability testing; Polyneuropathy.

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Figures

Fig. 1
Fig. 1
Motor nerve excitability measures including A: current-threshold relationship, B: strength-duration properties, C: threshold electrotonus, and D recovery cycle. Red: NCS+ PNP, green: NCS− PNP, blue: No polyneuropathy. Data shown as mean ± SD. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2
Fig. 2
Correlations between NET and conventional NCS. Sural nerve amplitude and subexcitability (r = 0.6309; p = 0.018), tibial nerve motor amplitude and rheobase (r = −0.4139; p = 0.044), peroneal nerve F-wave latency and subexcitability (r = −0.5525; p = 0.010) and tibial nerve F-wave-latency and subexcitability (r = −0.5408; p = 0.004) were significantly correlated.
Fig. 3
Fig. 3
Correlations between NET and clinical neuropathy scores and vibration detection threshold (VDT). Correlations were not statistically significant.

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