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Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling

PURPOSE: To quantify visual field (VF) variability as a function of threshold sensitivity and location, and to compare weighted pointwise linear regression (PLR) with unweighted PLR and pointwise exponential regression (PER) for data fit and prediction ability. METHODS: Two datasets were used for th...

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Autores principales: Rabiolo, Alessandro, Morales, Esteban, Afifi, Abdelmonem A, Yu, Fei, Nouri-Mahdavi, Kouros, Caprioli, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798312/
https://www.ncbi.nlm.nih.gov/pubmed/31637105
http://dx.doi.org/10.1167/tvst.8.5.25
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author Rabiolo, Alessandro
Morales, Esteban
Afifi, Abdelmonem A
Yu, Fei
Nouri-Mahdavi, Kouros
Caprioli, Joseph
author_facet Rabiolo, Alessandro
Morales, Esteban
Afifi, Abdelmonem A
Yu, Fei
Nouri-Mahdavi, Kouros
Caprioli, Joseph
author_sort Rabiolo, Alessandro
collection PubMed
description PURPOSE: To quantify visual field (VF) variability as a function of threshold sensitivity and location, and to compare weighted pointwise linear regression (PLR) with unweighted PLR and pointwise exponential regression (PER) for data fit and prediction ability. METHODS: Two datasets were used for this retrospective study. The first was used to characterize and estimate VF variability, and included a total of 4,747 eyes of 3,095 glaucoma patients with six or more VFs and 3 years or more of follow-up. After performing PER for each series, standard deviation of residuals was quantified for each decibel of sensitivity as a measure of variability. A separate dataset was used to test and compare unweighted PLR, weighted PLR, and PER for data fit and prediction, and included 261 eyes of 176 primary open-angle glaucoma patients with 10 or more VFs and 6 years or more of follow-up. RESULTS: The degree of variability changed as a function of threshold sensitivity with a zenith and a nadir at 33 and 11 dB, respectively. Variability decreased with eccentricity and was higher in the central 10° (P < 0.001). Differences among the methods for data fit were negligible. PER was the best model to predict future sensitivity values in the mid term and long term. CONCLUSIONS: VF variability increases with the severity of glaucoma damage and decreases with eccentricity. Weighted linear regression neither improves model fit nor prediction. PER exhibited the best prediction ability, which is likely related to the nonlinear nature of long-term glaucomatous perimetric decay. TRANSLATIONAL RELEVANCE: This study suggests that taking into account heteroscedasticity has no advantage in VF modeling.
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spelling pubmed-67983122019-10-21 Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling Rabiolo, Alessandro Morales, Esteban Afifi, Abdelmonem A Yu, Fei Nouri-Mahdavi, Kouros Caprioli, Joseph Transl Vis Sci Technol Articles PURPOSE: To quantify visual field (VF) variability as a function of threshold sensitivity and location, and to compare weighted pointwise linear regression (PLR) with unweighted PLR and pointwise exponential regression (PER) for data fit and prediction ability. METHODS: Two datasets were used for this retrospective study. The first was used to characterize and estimate VF variability, and included a total of 4,747 eyes of 3,095 glaucoma patients with six or more VFs and 3 years or more of follow-up. After performing PER for each series, standard deviation of residuals was quantified for each decibel of sensitivity as a measure of variability. A separate dataset was used to test and compare unweighted PLR, weighted PLR, and PER for data fit and prediction, and included 261 eyes of 176 primary open-angle glaucoma patients with 10 or more VFs and 6 years or more of follow-up. RESULTS: The degree of variability changed as a function of threshold sensitivity with a zenith and a nadir at 33 and 11 dB, respectively. Variability decreased with eccentricity and was higher in the central 10° (P < 0.001). Differences among the methods for data fit were negligible. PER was the best model to predict future sensitivity values in the mid term and long term. CONCLUSIONS: VF variability increases with the severity of glaucoma damage and decreases with eccentricity. Weighted linear regression neither improves model fit nor prediction. PER exhibited the best prediction ability, which is likely related to the nonlinear nature of long-term glaucomatous perimetric decay. TRANSLATIONAL RELEVANCE: This study suggests that taking into account heteroscedasticity has no advantage in VF modeling. The Association for Research in Vision and Ophthalmology 2019-10-17 /pmc/articles/PMC6798312/ /pubmed/31637105 http://dx.doi.org/10.1167/tvst.8.5.25 Text en Copyright 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Articles
Rabiolo, Alessandro
Morales, Esteban
Afifi, Abdelmonem A
Yu, Fei
Nouri-Mahdavi, Kouros
Caprioli, Joseph
Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title_full Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title_fullStr Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title_full_unstemmed Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title_short Quantification of Visual Field Variability in Glaucoma: Implications for Visual Field Prediction and Modeling
title_sort quantification of visual field variability in glaucoma: implications for visual field prediction and modeling
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798312/
https://www.ncbi.nlm.nih.gov/pubmed/31637105
http://dx.doi.org/10.1167/tvst.8.5.25
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