Literature DB >> 1375882

Amplitude abnormalities in the scalp far-field N18 of SSEPs to median nerve stimulation in patients with midbrain-pontine lesion.

E Urasaki1, S Wada, C Kadoya, T Tokimura, A Yokota, S Yamamoto, A Fukumura, S Hamada.   

Abstract

Various amplitude ratios were measured in 20 normal controls and 36 patients with midbrain-pontine, thalamic or putaminal lesions in order to evaluate the amplitude abnormalities in scalp far-field N18 following median nerve stimulation. A study of normal controls showed that the distributions of P9/N18, P14/N18 and N18/P14 + N18 resembled a gaussian distribution and could be used as criteria for determining the decrease in N18 amplitude in each patient. There was a decrease in N18 amplitude, or the absence of N18, in patients with midbrain-pontine lesions, but not in those with thalamic or putaminal lesions. Nine amplitude ratios (P11/P9, P14/P9, N18/P9, P9/P11, P9/P14, P9/N18, N18/P14, P14/N18 and N18/P14 + N18) were compared statistically for normal controls and 3 groups of patients based on non-parametric, Wilcoxon's non-pairs and signed-rank tests. A decrease in N18 amplitude in midbrain-pontine lesion was shown by significant changes in N18/P9, P9/N18, N18/P14, P14/N18 and N18/P14 + N18, no amplitude decreases in P11 and P14 being found from the amplitude ratios of P11/P9, P9/P11, P14/P9 and P9/P14. No significant changes were seen in any of the 9 amplitude ratios when the normal controls and patients with thalamic and putaminal lesions were compared. The amplitude ratios of N18 can be used to detect a decrease in N18 amplitude in patients with midbrain-pontine lesions. The data obtained support the hypothesis that N18 originates in the midbrain-pontine region and that neither the thalamus nor thalamocortical radiation make major contributions to the formation of the N18 peak.

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Year:  1992        PMID: 1375882     DOI: 10.1016/0168-5597(92)90004-u

Source DB:  PubMed          Journal:  Electroencephalogr Clin Neurophysiol        ISSN: 0013-4694


  2 in total

1.  Brainstem origins of the n18 component of the somatosensory evoked response.

Authors:  M Philips; M Kotapka; T Patterson; D C Bigelow; E Zager; E S Flamm; M Stecker
Journal:  Skull Base Surg       Date:  1998

2.  The origin, and application of somatosensory evoked potentials as a neurophysiological technique to investigate neuroplasticity.

Authors:  Steven R Passmore; Bernadette Murphy; Timothy D Lee
Journal:  J Can Chiropr Assoc       Date:  2014-06
  2 in total

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