4.5 Article

Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis

Journal

Publisher

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/tvst.10.4.1

Keywords

principal component analysis; visual evoked potentials; pediatric; development

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Funding

  1. National Institute of Neurological Disorders and Stroke of the National Institutes of Health [R01NS0975NIH]
  2. Pennsylvania Department of Health [SAP100077078]
  3. American Academy of Neurology Clinical Research Scholarship
  4. International Headache Academy Research Fellowship
  5. Minds Matter Frontiers grant from the Children's Hospital of Philadelphia
  6. Department of Defense [W81XWH-151-0447]

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The study used Principal Component Analysis (PCA) to characterize developmental changes of prVEP in youths, revealing narrowing and amplitude reduction of the P100 peak with maturation, as well as a broader and smaller P100 peak in male subjects compared to female subjects.
Purpose: Peak amplitude and peak latency in the pattern reversal visual evoked potential (prVEP) vary with maturation. We considered that principal component analysis (PCA) may be used to describe age-related variation over the entire prVEP time course and provide a means of modeling and removing variation due to developmental age. Methods: PrVEP was recorded from 155 healthy subjects ages 11 to 19 years at two time points. We created a model of the prVEP by identifying principal components (PCs) that explained >95% of the variance in a training dataset of 40 subjects. We examined the ability of the PCs to explain variance in an age- and sex-matched validation dataset (n = 40) and calculated the intrasubject reliability of the PC coefficients between the two time points. We explored the effect of subject age and sex upon the PC coefficients. Results: Seven PCs accounted for 96.0% of the variability of the training dataset and 90.5% of the variability in the validation dataset with good within-subject reliability across time points (R > 0.7 for all PCs). The PCA model revealed narrowing and amplitude reduction of the P100 peak with maturation, and a broader and smaller P100 peak in male subjects compared to female subjects. Conclusions: PCA is a generalizable, reliable, and unbiased method of analyzing prVEP. The PCA model revealed changes across maturation and biological sex not fully described by standard peak analysis. Translational Relevance: We describe a novel application of PCA to characterize developmental changes of prVEP in youths that can be used to compare healthy and pathologic pediatric cohorts.

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