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Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions

PURPOSE: To compare the ability of linear mixed models with different random effect distributions to estimate rates of visual field loss in glaucoma patients. METHODS: Eyes with five or more reliable standard automated perimetry (SAP) tests were identified from the Duke Glaucoma Registry. Mean devia...

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Autores principales: Swaminathan, Swarup S., Berchuck, Samuel I., Jammal, Alessandro A., Rao, J. Sunil, Medeiros, Felipe A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842468/
https://www.ncbi.nlm.nih.gov/pubmed/35138343
http://dx.doi.org/10.1167/tvst.11.2.16
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author Swaminathan, Swarup S.
Berchuck, Samuel I.
Jammal, Alessandro A.
Rao, J. Sunil
Medeiros, Felipe A.
author_facet Swaminathan, Swarup S.
Berchuck, Samuel I.
Jammal, Alessandro A.
Rao, J. Sunil
Medeiros, Felipe A.
author_sort Swaminathan, Swarup S.
collection PubMed
description PURPOSE: To compare the ability of linear mixed models with different random effect distributions to estimate rates of visual field loss in glaucoma patients. METHODS: Eyes with five or more reliable standard automated perimetry (SAP) tests were identified from the Duke Glaucoma Registry. Mean deviation (MD) values from each visual field and associated timepoints were collected. These data were modeled using ordinary least square (OLS) regression and linear mixed models using the Gaussian, Student's t, or log-gamma (LG) distributions as the prior distribution for random effects. Model fit was compared using the Watanabe–Akaike information criterion (WAIC). Simulated eyes of varying initial disease severity and rates of progression were created to assess the accuracy of each model in predicting the rate of change and likelihood of declaring progression. RESULTS: A total of 52,900 visual fields from 6558 eyes of 3981 subjects were included. Mean follow-up period was 8.7 ± 4.0 years, with an average of 8.1 ± 3.7 visual fields per eye. The LG model produced the lowest WAIC, demonstrating optimal model fit. In simulations, the LG model declared progression earlier than OLS (P < 0.001) and had the greatest accuracy in predicted slopes (P < 0.001). The Gaussian model significantly underestimated rates of progression among fast and catastrophic progressors. CONCLUSIONS: Linear mixed models using the LG distribution outperformed conventional approaches for estimating rates of SAP MD loss in a population with glaucoma. TRANSLATIONAL RELEVANCE: Use of the LG distribution in models estimating rates of change among glaucoma patients may improve their accuracy in rapidly identifying progressors at high risk for vision loss.
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spelling pubmed-88424682022-02-18 Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions Swaminathan, Swarup S. Berchuck, Samuel I. Jammal, Alessandro A. Rao, J. Sunil Medeiros, Felipe A. Transl Vis Sci Technol Article PURPOSE: To compare the ability of linear mixed models with different random effect distributions to estimate rates of visual field loss in glaucoma patients. METHODS: Eyes with five or more reliable standard automated perimetry (SAP) tests were identified from the Duke Glaucoma Registry. Mean deviation (MD) values from each visual field and associated timepoints were collected. These data were modeled using ordinary least square (OLS) regression and linear mixed models using the Gaussian, Student's t, or log-gamma (LG) distributions as the prior distribution for random effects. Model fit was compared using the Watanabe–Akaike information criterion (WAIC). Simulated eyes of varying initial disease severity and rates of progression were created to assess the accuracy of each model in predicting the rate of change and likelihood of declaring progression. RESULTS: A total of 52,900 visual fields from 6558 eyes of 3981 subjects were included. Mean follow-up period was 8.7 ± 4.0 years, with an average of 8.1 ± 3.7 visual fields per eye. The LG model produced the lowest WAIC, demonstrating optimal model fit. In simulations, the LG model declared progression earlier than OLS (P < 0.001) and had the greatest accuracy in predicted slopes (P < 0.001). The Gaussian model significantly underestimated rates of progression among fast and catastrophic progressors. CONCLUSIONS: Linear mixed models using the LG distribution outperformed conventional approaches for estimating rates of SAP MD loss in a population with glaucoma. TRANSLATIONAL RELEVANCE: Use of the LG distribution in models estimating rates of change among glaucoma patients may improve their accuracy in rapidly identifying progressors at high risk for vision loss. The Association for Research in Vision and Ophthalmology 2022-02-09 /pmc/articles/PMC8842468/ /pubmed/35138343 http://dx.doi.org/10.1167/tvst.11.2.16 Text en Copyright 2022 The Authors https://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
Swaminathan, Swarup S.
Berchuck, Samuel I.
Jammal, Alessandro A.
Rao, J. Sunil
Medeiros, Felipe A.
Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title_full Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title_fullStr Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title_full_unstemmed Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title_short Rates of Glaucoma Progression Derived from Linear Mixed Models Using Varied Random Effect Distributions
title_sort rates of glaucoma progression derived from linear mixed models using varied random effect distributions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842468/
https://www.ncbi.nlm.nih.gov/pubmed/35138343
http://dx.doi.org/10.1167/tvst.11.2.16
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