Prediction of Visual Field Progression from OCT Structural Measures in Moderate to Advanced Glaucoma.


Journal

American journal of ophthalmology
ISSN: 1879-1891
Titre abrégé: Am J Ophthalmol
Pays: United States
ID NLM: 0370500

Informations de publication

Date de publication:
06 2021
Historique:
received: 27 09 2020
revised: 23 01 2021
accepted: 25 01 2021
pubmed: 3 2 2021
medline: 11 9 2021
entrez: 2 2 2021
Statut: ppublish

Résumé

To test the hypothesis that visual field (VF) progression can be predicted from baseline and longitudinal optical coherence tomography (OCT) structural measurements. Prospective cohort study. A total of 104 eyes (104 patients) with ≥3 years of follow-up and ≥5 VF examinations were enrolled. We defined VF progression based on pointwise linear regression on 24-2 VF (≥3 locations with slope less than or equal to -1.0 dB/year and P < .01). We used elastic net logistic regression (ENR) and machine learning to predict VF progression with demographics, baseline circumpapillary retinal nerve fiber layer (RNFL), macular ganglion cell/inner plexiform layer (GCIPL) thickness, and RNFL and GCIPL change rates at central 24 superpixels and 3 eccentricities, 3.4°, 5.5°, and 6.8°, from fovea and hemimaculas. Areas-under-ROC curves (AUC) were used to compare models. Average ± SD follow-up and VF examinations were 4.5 ± 0.9 years and 8.7 ± 1.6, respectively. VF progression was detected in 23 eyes (22%). ENR selected rates of change of superotemporal RNFL sector and GCIPL change rates in 5 central superpixels and at 3.4° and 5.6° eccentricities as the best predictor subset (AUC = 0.79 ± 0.12). Best machine learning predictors consisted of baseline superior hemimacular GCIPL thickness and GCIPL change rates at 3.4° eccentricity and 3 central superpixels (AUC = 0.81 ± 0.10). Models using GCIPL-only structural variables performed better than RNFL-only models. VF progression can be predicted with clinically relevant accuracy from baseline and longitudinal structural data. Further refinement of proposed models would assist clinicians with timely prediction of functional glaucoma progression and clinical decision making.

Identifiants

pubmed: 33529590
pii: S0002-9394(21)00044-1
doi: 10.1016/j.ajo.2021.01.023
pmc: PMC8580576
mid: NIHMS1690784
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

172-181

Subventions

Organisme : NEI NIH HHS
ID : R01 EY029792
Pays : United States
Organisme : NEI NIH HHS
ID : R21 EY030142
Pays : United States
Organisme : NEI NIH HHS
ID : R21 EY031725
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

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Auteurs

Kouros Nouri-Mahdavi (K)

Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, California, USA. Electronic address: nouri-mahdavi@jsei.ucla.edu.

Vahid Mohammadzadeh (V)

Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, California, USA.

Alessandro Rabiolo (A)

Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, California, USA; Department of Ophthalmology, Gloucestershire Hospitals National Health Service Foundation Trust, Cheltenham, United Kingdom.

Kiumars Edalati (K)

Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, California, USA.

Joseph Caprioli (J)

Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, California, USA.

Siamak Yousefi (S)

Departments of Ophthalmology and Genetics, Genomics, and Informatics, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

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Classifications MeSH