Enlarged high frequency oscillations of the median nerve somatosensory evoked potential and survival in amyotrophic lateral sclerosis
•N20-P25 amplitude in the median nerve SEP was increased in amyotrophic lateral sclerosis (ALS), and associated with survival.•Early and late high frequency oscillations over N20 were enlarged in ALS.•Increased high frequency oscillation size in ALS might be a compensatory phenomenon. A large N20 an...
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Veröffentlicht in: | Clinical neurophysiology 2021-09, Vol.132 (9), p.2003-2011 |
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Zusammenfassung: | •N20-P25 amplitude in the median nerve SEP was increased in amyotrophic lateral sclerosis (ALS), and associated with survival.•Early and late high frequency oscillations over N20 were enlarged in ALS.•Increased high frequency oscillation size in ALS might be a compensatory phenomenon.
A large N20 and P25 of the median nerve somatosensory evoked potential (SEP) predicts short survival in amyotrophic lateral sclerosis (ALS). We investigated whether high frequency oscillations (HFOs) over N20 are enlarged and associated with survival in ALS.
A total of 145 patients with ALS and 57 healthy subjects were studied. We recorded the median nerve SEP and measured the onset-to-peak amplitude of N20 (N20o-p), and peak-to-peak amplitude between N20 and P25 (N20p-P25p). We obtained early and late HFO potentials by filtering SEP between 500 and 1 kHz, and measured the peak-to-peak amplitude. We followed up patients until endpoints (death or tracheostomy) and analyzed the relationship between SEP or HFO amplitudes and survival using a Cox analysis.
Patients showed larger N20o-p, N20p-P25p, and early and late HFO amplitudes than the control values. N20p-P25p was associated with survival periods (p = 0.0004), while early and late HFO amplitudes showed no significant association with survival (p = 0.4307, and p = 0.6858, respectively).
The HFO amplitude in ALS is increased, but does not predict survival.
The enlarged HFOs in ALS might be a compensatory phenomenon to the hyperexcitability of the sensory cortex pyramidal neurons. |
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ISSN: | 1388-2457 1872-8952 |
DOI: | 10.1016/j.clinph.2021.05.023 |