Abstract
We model longitudinal macular thickness measurements to monitor the course of glaucoma and prevent vision loss due to disease progression. The macular thickness varies over a 6 × 6 grid of locations on the retina, with additional variability arising from the imaging process at each visit. Currently, ophthalmologists estimate slopes using repeated simple linear regression for each subject and location. To estimate slopes more precisely, we develop a novel Bayesian hierarchical model for multiple subjects with spatially varying population-level and subject-level coefficients, borrowing information over subjects and measurement locations. We augment the model with visit effects to account for observed spatially correlated visit-specific errors. We model spatially varying: (a) intercepts, (b) slopes, and (c) log-residual standard deviations (SD) with multivariate Gaussian process priors with Matérn cross-covariance functions. Each marginal process assumes an exponential kernel with its own SD and spatial correlation matrix. We develop our models for and apply them to data from the Advanced Glaucoma Progression Study. We show that including visit effects in the model reduces error in predicting future thickness measurements and greatly improves model fit.
Funding Statement
This work was supported by an NIH R01 grant (R01-EY029792), an unrestricted Departmental Grant from Research to Prevent Blindness, and an unrestricted grant from Heidelberg Engineering.
AJH was supported by NIH Grant K25 AI153816, NSF Grant DMS 2152774, and a generous gift from the Karen Toffler Charitable Trust.
Acknowledgments
This work used computational and storage services associated with the Hoffman2 Shared Cluster provided by UCLA Office of Advanced Research Computing’s Research Technology Group.
Citation
Erica Su. Robert E. Weiss. Kouros Nouri-Mahdavi. Andrew J. Holbrook. "A spatially varying hierarchical random effects model for longitudinal macular structural data in glaucoma patients." Ann. Appl. Stat. 18 (4) 3444 - 3466, December 2024. https://doi.org/10.1214/24-AOAS1944
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