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

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 va...

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Autores principales: Patterson Gentile, Carlyn, Joshi, Nabin R., Ciuffreda, Kenneth J., Arbogast, Kristy B., Master, Christina, Aguirre, Geoffrey K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024780/
https://www.ncbi.nlm.nih.gov/pubmed/34003980
http://dx.doi.org/10.1167/tvst.10.4.1
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author Patterson Gentile, Carlyn
Joshi, Nabin R.
Ciuffreda, Kenneth J.
Arbogast, Kristy B.
Master, Christina
Aguirre, Geoffrey K.
author_facet Patterson Gentile, Carlyn
Joshi, Nabin R.
Ciuffreda, Kenneth J.
Arbogast, Kristy B.
Master, Christina
Aguirre, Geoffrey K.
author_sort Patterson Gentile, Carlyn
collection PubMed
description 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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spelling pubmed-80247802021-04-16 Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis Patterson Gentile, Carlyn Joshi, Nabin R. Ciuffreda, Kenneth J. Arbogast, Kristy B. Master, Christina Aguirre, Geoffrey K. Transl Vis Sci Technol Article 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. The Association for Research in Vision and Ophthalmology 2021-04-01 /pmc/articles/PMC8024780/ /pubmed/34003980 http://dx.doi.org/10.1167/tvst.10.4.1 Text en Copyright 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Article
Patterson Gentile, Carlyn
Joshi, Nabin R.
Ciuffreda, Kenneth J.
Arbogast, Kristy B.
Master, Christina
Aguirre, Geoffrey K.
Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title_full Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title_fullStr Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title_full_unstemmed Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title_short Developmental Effects on Pattern Visual Evoked Potentials Characterized by Principal Component Analysis
title_sort developmental effects on pattern visual evoked potentials characterized by principal component analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024780/
https://www.ncbi.nlm.nih.gov/pubmed/34003980
http://dx.doi.org/10.1167/tvst.10.4.1
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