Literature DB >> 28056389

Altered visual contrast gain control is sensitive for idiopathic generalized epilepsies.

Daehan Won1, Wonsuk Kim2, W Art Chaovalitwongse3, Jeffrey J Tsai4.   

Abstract

OBJECTIVE: Visual hyperexcitability in the form of abnormal contrast gain control has been shown in photosensitive epilepsy and idiopathic generalized epilepsies. We assessed the accuracy and reliability of measures of visual contrast gain control in discerning individuals with idiopathic generalized epilepsies from healthy controls.
METHODS: Twenty-four adult patients with idiopathic generalized epilepsy and 32 neurotypical control subjects from two study sites participated in a prospective, cross-sectional study. We recorded steady-state visual evoked potentials to a wide range of contrasts of a flickering grating stimulus. The resultant response magnitude vs. contrast curves were fitted to a standard model of contrast response function, and the model parameters were used as input features to a linear classifier to separate patients from controls. Additionally we compared the relative contribution of model parameters towards the classification using a sparse feature-selection approach.
RESULTS: Classification accuracy was 80% or better. Sensitivity and specificity both were 80-85%. Cross validation confirmed robust classifier performance generalizable across the data from the two samples. Patients' relative lack of gain control at high contrasts was the most important information distinguishing patients from controls.
CONCLUSIONS: Individuals with idiopathic generalized epilepsy were distinguishable from the neurotypical with a high degree of accuracy and reliability by a reduction in gain control at high contrasts. SIGNIFICANCE: Gain control is an essential neural operation that regulates neuronal sensitivity to stimuli and may represent a novel biomarker of hyperexcitability. Published by Elsevier B.V.

Entities:  

Keywords:  Biomarker; Hyperexcitability; Machine learning; Visual-evoked potentials

Mesh:

Year:  2016        PMID: 28056389      PMCID: PMC5823846          DOI: 10.1016/j.clinph.2016.12.008

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


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