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DOI 10.1016/j.clinph.2003.10.018

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2004

Principal component analysis for reduction of ocular artefacts in event-related potentials of normal and dyslexic children.

Casarotto Silvia, Bianchi Anna M, Cerutti Sergio, Chiarenza Giuseppe A

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Аннотация

OBJECTIVE

The aim of this study was to reduce ocular artefacts in single trial event-related potentials (ERPs) recorded in normal and in dyslexic children.

METHODS

ERPs were recorded during passive and active reading of centrally presented alphabetic letters and non alphabetic symbols. EEG was recorded from 10 EEG locations using the 10-20 system. Diagonal EOG from the right eye was also recorded. Principal component analysis (PCA) was applied in order to reduce ocular artefacts: the first or the second principal component (PC) was subtracted when the correlation coefficient between the component and EOG was greater or equal to 0.9 or 0.95, respectively. Performance of the method was tested on simulated and real data, on both single and averaged trials, varying EOG amplitude and artefact transmission characteristics.

RESULTS

Applying the method to real recordings from normal and dyslexic children, we obtained a significant increase in the number of useful trials. In normal children we retrieved 41.0% of the rejected trials in passive and 39.1% in active reading. In dyslexic children 36.7 and 32.2% of the rejected trials in passive and active reading could be included in the respective averages.

CONCLUSIONS

The method allows an increase in the number of trials suitable for averaging, a great improvement in ERP quality and a reduction in the recording time.

Для цитирования: Casarotto Silvia, Bianchi Anna M, Cerutti Sergio, Chiarenza Giuseppe A. Principal component analysis for reduction of ocular artefacts in event-related potentials of normal and dyslexic children.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2004. DOI: 10.1016/j.clinph.2003.10.018.

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