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DOI 10.1016/j.clinph.2014.01.027

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2014

Variability of magnetoencephalographic sensor sensitivity measures as a function of age, brain volume and cortical area.

Irimia Andrei, Erhart Matthew J, Brown Timothy T

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To assess the feasibility and appropriateness of magnetoencephalography (MEG) for both adult and pediatric studies, as well as for the developmental comparison of these factors across a wide range of ages.

METHODS

For 45 subjects with ages from 1 to 24years (infants, toddlers, school-age children and young adults), lead fields (LFs) of MEG sensors are computed using anatomically realistic boundary element models (BEMs) and individually-reconstructed cortical surfaces. Novel metrics are introduced to quantify MEG sensor focality.

RESULTS

The variability of MEG focality is graphed as a function of brain volume and cortical area. Statistically significant differences in total cerebral volume, cortical area, MEG global sensitivity and LF focality are found between age groups.

CONCLUSIONS

Because MEG focality and sensitivity differ substantially across the age groups studied, the cortical LF maps explored here can provide important insights for the examination and interpretation of MEG signals from early childhood to young adulthood.

SIGNIFICANCE: This is the first study to (1) investigate the relationship between MEG cortical LFs and brain volume as well as cortical area across development, and (2) compare LFs between subjects with different head sizes using detailed cortical reconstructions.

Для цитирования: Irimia Andrei, Erhart Matthew J, Brown Timothy T. Variability of magnetoencephalographic sensor sensitivity measures as a function of age, brain volume and cortical area.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2014. DOI: 10.1016/j.clinph.2014.01.027.

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