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Multicenter Normative Data for Mesopic Microperimetry.
Maximilian Pfau1,2,3,4, Jasleen K Jolly5,6,7, Jason Charng8,9,10
1Department of Ophthalmology, University Hospital Basel, Basel, Switzerland.
Investigative Ophthalmology & Visual Science
|October 18, 2024
Summary
A large dataset for the Macular Integrity Assessment (MAIA) microperimeter was created. A simple linear model effectively explains normal variations in visual sensitivity, making it useful for customized testing.
Area of Science:
- Ophthalmology
- Visual Neuroscience
- Biostatistics
Background:
- Microperimetry is crucial for assessing visual function.
- Establishing normative data is essential for accurate interpretation of microperimetry results.
- Existing models for predicting visual sensitivity may require refinement.
Purpose of the Study:
- To establish a large, multi-center normative dataset for the Macular Integrity Assessment (MAIA) microperimeter.
- To compare the goodness-of-fit and prediction accuracy of various hill-of-vision models.
- To identify the most effective model for predicting normative visual sensitivity.
Main Methods:
- Included microperimetry data from 1137 tests on 531 healthy eyes across multiple study groups.
- Employed linear mixed models (LMMs) to develop interpretable hill-of-vision models.
- Utilized cross-validation with site-wise splits to compare regression models, evaluating Mean Absolute Error (MAE) and miscalibration area.
Main Results:
- A Bayesian mixed model showed the lowest MAE (2.13 dB) and miscalibration area (0.13).
- A parsimonious linear model demonstrated comparable performance with an MAE of 2.17 dB and miscalibration area of 0.14.
- Both models effectively predicted normative visual sensitivity based on age and eccentricity.
Conclusions:
- Normal variations in mesopic microperimetry visual sensitivity are well-explained by a linear model incorporating age and eccentricity.
- The developed dataset and code vignette facilitate the estimation of normative values for customized microperimeter testing patterns.
- The findings support the use of simplified models for understanding visual sensitivity across diverse retinal locations.
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