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. 2016 Mar 9:8:50.
doi: 10.3389/fnagi.2016.00050. eCollection 2016.

Differences in F-Wave Characteristics between Spinobulbar Muscular Atrophy and Amyotrophic Lateral Sclerosis

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Differences in F-Wave Characteristics between Spinobulbar Muscular Atrophy and Amyotrophic Lateral Sclerosis

Jia Fang et al. Front Aging Neurosci. .

Abstract

There is limited data on the differences in F-wave characteristics between spinobulbar muscular atrophy (SBMA) and lower motor neuron dominant (LMND) amyotrophic lateral sclerosis (ALS). We compared the parameters of F-waves recorded bilaterally from the median, ulnar, tibial, and deep peroneal nerves in 32 SBMA patients, 37 patients with LMND ALS, and 30 normal controls. The maximum F-wave amplitudes, frequencies of giant F-waves, and frequencies of patients with giant F-waves in all nerves examined were significantly higher in the SBMA patients than in the ALS patients and the normal controls. The mean F-wave amplitude, maximum F-wave amplitude, frequency of giant F-waves, and frequency of patients with giant F-waves in the median and deep peroneal nerves were comparable between the ALS patients and normal controls. Giant F-waves were detected in multiple nerves and were often symmetrical in the SBMA patients compared with the ALS patients. The number of nerves with giant F-waves seems to be the most robust variable for differentiation of SBMA from ALS, with an area under the curve of 0.908 (95% CI: 0.835-0.982). A cut-off value of the number of nerves with giant F-waves (≥3) for diagnosing SBMA showed high sensitivity and specificity: 85% sensitivity and 81% specificity vs. ALS patients. No significant correlations were found between the pooled frequency of giant F-waves and disease duration in the SBMA (r = 0.162, P = 0.418) or ALS groups (r = 0.107, P = 0.529). Our findings suggested that F-waves might be used to discriminate SBMA from ALS, even at early stages of disease.

Keywords: F-wave; amyotrophic lateral sclerosis; giant F-wave; motor neuron; nerve conduction study; spinobulbar muscular atrophy.

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Figures

FIGURE 1
FIGURE 1
Histogram of frequencies of subjects exhibiting giant F-waves in different numbers of nerves in the spinobulbar muscular atrophy (SBMA) patients, the amyotrophic lateral sclerosis (ALS) patients, and the normal controls. Ordinate, frequency of subjects with giant F-waves in different numbers of nerves. Abscissa, number of nerves with giant F-waves.
FIGURE 2
FIGURE 2
Histogram of frequencies of giant F-waves recorded symmetrically between the left and right sides in the spinobulbar muscular atrophy (SBMA) patients, the ALS patients, and the normal controls. Ordinate, frequency of giant F-waves recorded symmetrically between the left and right sides. The frequency of symmetrical giant F-waves between the left and right sides in the SBMA patients was significantly higher than those in the ALS patients (P = 0.004) and the normal controls (P = 0.001). While the frequencies of symmetrical giant F-waves were comparable between the ALS patients and the normal controls (P = 0.171). P < 0.05.

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