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Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation
BACKGROUND: To model the progression of geographic atrophy (GA) in patients with age-related macular degeneration (AMD) by building a suitable statistical regression model for GA size measurements obtained from fundus autofluorescence imaging. METHODS: Based on theoretical considerations, we develop...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369742/ https://www.ncbi.nlm.nih.gov/pubmed/34404346 http://dx.doi.org/10.1186/s12874-021-01356-0 |
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author | Behning, Charlotte Fleckenstein, Monika Pfau, Maximilian Adrion, Christine Goerdt, Lukas Lindner, Moritz Schmitz-Valckenberg, Steffen Holz, Frank G Schmid, Matthias |
author_facet | Behning, Charlotte Fleckenstein, Monika Pfau, Maximilian Adrion, Christine Goerdt, Lukas Lindner, Moritz Schmitz-Valckenberg, Steffen Holz, Frank G Schmid, Matthias |
author_sort | Behning, Charlotte |
collection | PubMed |
description | BACKGROUND: To model the progression of geographic atrophy (GA) in patients with age-related macular degeneration (AMD) by building a suitable statistical regression model for GA size measurements obtained from fundus autofluorescence imaging. METHODS: Based on theoretical considerations, we develop a linear mixed-effects model for GA size progression that incorporates covariable-dependent enlargement rates as well as correlations between longitudinally collected GA size measurements. To capture nonlinear progression in a flexible way, we systematically assess Box-Cox transformations with different transformation parameters λ. Model evaluation is performed on data collected for two longitudinal, prospective multi-center cohort studies on GA size progression. RESULTS: A transformation parameter of λ=0.45 yielded the best model fit regarding the Akaike information criterion (AIC). When hypertension and hypercholesterolemia were included as risk factors in the model, they showed an association with progression of GA size. The mean estimated age-of-onset in this model was 67.21±6.49 years. CONCLUSIONS: We provide a comprehensive framework for modeling the course of uni- or bilateral GA size progression in longitudinal observational studies. Specifically, the model allows for age-of-onset estimation, identification of risk factors and prediction of future GA size. A square-root transformation of atrophy size is recommended before model fitting. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12874-021-01356-0). |
format | Online Article Text |
id | pubmed-8369742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83697422021-08-18 Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation Behning, Charlotte Fleckenstein, Monika Pfau, Maximilian Adrion, Christine Goerdt, Lukas Lindner, Moritz Schmitz-Valckenberg, Steffen Holz, Frank G Schmid, Matthias BMC Med Res Methodol Research BACKGROUND: To model the progression of geographic atrophy (GA) in patients with age-related macular degeneration (AMD) by building a suitable statistical regression model for GA size measurements obtained from fundus autofluorescence imaging. METHODS: Based on theoretical considerations, we develop a linear mixed-effects model for GA size progression that incorporates covariable-dependent enlargement rates as well as correlations between longitudinally collected GA size measurements. To capture nonlinear progression in a flexible way, we systematically assess Box-Cox transformations with different transformation parameters λ. Model evaluation is performed on data collected for two longitudinal, prospective multi-center cohort studies on GA size progression. RESULTS: A transformation parameter of λ=0.45 yielded the best model fit regarding the Akaike information criterion (AIC). When hypertension and hypercholesterolemia were included as risk factors in the model, they showed an association with progression of GA size. The mean estimated age-of-onset in this model was 67.21±6.49 years. CONCLUSIONS: We provide a comprehensive framework for modeling the course of uni- or bilateral GA size progression in longitudinal observational studies. Specifically, the model allows for age-of-onset estimation, identification of risk factors and prediction of future GA size. A square-root transformation of atrophy size is recommended before model fitting. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12874-021-01356-0). BioMed Central 2021-08-17 /pmc/articles/PMC8369742/ /pubmed/34404346 http://dx.doi.org/10.1186/s12874-021-01356-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Behning, Charlotte Fleckenstein, Monika Pfau, Maximilian Adrion, Christine Goerdt, Lukas Lindner, Moritz Schmitz-Valckenberg, Steffen Holz, Frank G Schmid, Matthias Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title | Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title_full | Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title_fullStr | Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title_full_unstemmed | Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title_short | Modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
title_sort | modeling of atrophy size trajectories: variable transformation, prediction and age-of-onset estimation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369742/ https://www.ncbi.nlm.nih.gov/pubmed/34404346 http://dx.doi.org/10.1186/s12874-021-01356-0 |
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