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Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment

It has been postulated that particular patterns of macular pigment (MP) distribution may be associated with the risk for eye diseases such as age-related macular degeneration (AMD). This work investigates the potential of Zernike polynomials (ZP) to characterise the level and distribution of MP, and...

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Autores principales: Allen, Piers, Calcagni, Antonio, Robson, Anthony G., Claridge, Ela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534297/
https://www.ncbi.nlm.nih.gov/pubmed/31125363
http://dx.doi.org/10.1371/journal.pone.0217265
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author Allen, Piers
Calcagni, Antonio
Robson, Anthony G.
Claridge, Ela
author_facet Allen, Piers
Calcagni, Antonio
Robson, Anthony G.
Claridge, Ela
author_sort Allen, Piers
collection PubMed
description It has been postulated that particular patterns of macular pigment (MP) distribution may be associated with the risk for eye diseases such as age-related macular degeneration (AMD). This work investigates the potential of Zernike polynomials (ZP) to characterise the level and distribution of MP, and their suitability as a representation for analysis of the effects of age and AMD on MP patterns. As the case study, MP distribution maps computed using an experimental method based on fundus reflectance (MRIA) were obtained for ninety volunteers representing three groups: under-fifty without AMD, fifty and over without AMD, and fifty and over with AMD. ZP with 105 coefficients were fitted to the maps using least-squares optimisation and found to represent MP maps accurately (RMSE<10(−1)). One-way MANOVA analysis carried out on ZP representations showed that the three subject groups have significantly different means (Wilk’s Lambda 0.125, p<0.0001). Linear discriminant analysis with leave-one-out scheme resulted in accuracy, sensitivity and specificity of classification according to, respectively, disease status regardless of age (81% all); disease status in the age-matched groups (87%, 88%, 86%); age irrespective of disease status (81%, 83%, 73%); and age for subjects without AMD (83%, 88%, 80%). Mean MP distributions computed from ZP coefficients for the three groups showed more elevated and more peaked MP for the healthy under-fifty group; more irregular and more elevated peripheral levels in over-fifty AMD group than in over-fifty non-AMD group; and moderate radial asymmetry in non-AMD over-50 group. The results suggest that ZP coefficients are capable of accurately representing MP in a way that captures certain spatial patterns of its distribution. Using the ZP representation MP maps could be classified according to both age and disease status with accuracy significantly greater than chance, with peak elevation, pattern irregularity and radial asymmetry identified as important features.
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spelling pubmed-65342972019-06-05 Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment Allen, Piers Calcagni, Antonio Robson, Anthony G. Claridge, Ela PLoS One Research Article It has been postulated that particular patterns of macular pigment (MP) distribution may be associated with the risk for eye diseases such as age-related macular degeneration (AMD). This work investigates the potential of Zernike polynomials (ZP) to characterise the level and distribution of MP, and their suitability as a representation for analysis of the effects of age and AMD on MP patterns. As the case study, MP distribution maps computed using an experimental method based on fundus reflectance (MRIA) were obtained for ninety volunteers representing three groups: under-fifty without AMD, fifty and over without AMD, and fifty and over with AMD. ZP with 105 coefficients were fitted to the maps using least-squares optimisation and found to represent MP maps accurately (RMSE<10(−1)). One-way MANOVA analysis carried out on ZP representations showed that the three subject groups have significantly different means (Wilk’s Lambda 0.125, p<0.0001). Linear discriminant analysis with leave-one-out scheme resulted in accuracy, sensitivity and specificity of classification according to, respectively, disease status regardless of age (81% all); disease status in the age-matched groups (87%, 88%, 86%); age irrespective of disease status (81%, 83%, 73%); and age for subjects without AMD (83%, 88%, 80%). Mean MP distributions computed from ZP coefficients for the three groups showed more elevated and more peaked MP for the healthy under-fifty group; more irregular and more elevated peripheral levels in over-fifty AMD group than in over-fifty non-AMD group; and moderate radial asymmetry in non-AMD over-50 group. The results suggest that ZP coefficients are capable of accurately representing MP in a way that captures certain spatial patterns of its distribution. Using the ZP representation MP maps could be classified according to both age and disease status with accuracy significantly greater than chance, with peak elevation, pattern irregularity and radial asymmetry identified as important features. Public Library of Science 2019-05-24 /pmc/articles/PMC6534297/ /pubmed/31125363 http://dx.doi.org/10.1371/journal.pone.0217265 Text en © 2019 Allen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Allen, Piers
Calcagni, Antonio
Robson, Anthony G.
Claridge, Ela
Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title_full Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title_fullStr Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title_full_unstemmed Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title_short Investigating the potential of Zernike polynomials to characterise spatial distribution of macular pigment
title_sort investigating the potential of zernike polynomials to characterise spatial distribution of macular pigment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534297/
https://www.ncbi.nlm.nih.gov/pubmed/31125363
http://dx.doi.org/10.1371/journal.pone.0217265
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