Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal Hypoplasia.

BCVA, best-corrected visual acuity CHS, Chediak–Higashi syndrome D, diopters FH, foveal hypoplasia Foveal hypoplasia GAN, generative adversarial network Generative adversarial network HPS, Hermansky–Pudlak syndrome LogMAR, logarithm of the minimal angle of resolution NEI, National Eye Institute Neural network classifier Nystagmus OCT PAX6, Paired Box 6 gene SER, spherical equivalent refractive error WAGR, Wilms tumor-aniridia-genital anomalies-retardation syndrome

Journal

Ophthalmology science
ISSN: 2666-9145
Titre abrégé: Ophthalmol Sci
Pays: Netherlands
ID NLM: 9918230896206676

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 02 06 2022
revised: 30 08 2022
accepted: 19 09 2022
entrez: 7 11 2022
pubmed: 8 11 2022
medline: 8 11 2022
Statut: epublish

Résumé

To describe the relationships between foveal structure and visual function in a cohort of individuals with foveal hypoplasia (FH) and to estimate FH grade and visual acuity using a deep learning classifier. Retrospective cohort study and experimental study. A total of 201 patients with FH were evaluated at the National Eye Institute from 2004 to 2018. Structural components of foveal OCT scans and corresponding clinical data were analyzed to assess their contributions to visual acuity. To automate FH scoring and visual acuity correlations, we evaluated the following 3 inputs for training a neural network predictor: (1) OCT scans, (2) OCT scans and metadata, and (3) real OCT scans and fake OCT scans created from a generative adversarial network. The relationships between visual acuity outcomes and determinants, such as foveal morphology, nystagmus, and refractive error. The mean subject age was 24.4 years (range, 1-73 years; standard deviation = 18.25 years) at the time of OCT imaging. The mean best-corrected visual acuity (n = 398 eyes) was equivalent to a logarithm of the minimal angle of resolution (LogMAR) value of 0.75 (Snellen 20/115). Spherical equivalent refractive error (SER) ranged from -20.25 diopters (D) to +13.63 D with a median of +0.50 D. The presence of nystagmus and a high-LogMAR value showed a statistically significant relationship ( Nystagmus and foveal anatomy impact visual outcomes in patients with FH, and computational algorithms reliably estimate FH grading and visual acuity.

Identifiants

pubmed: 36339947
doi: 10.1016/j.xops.2022.100225
pii: S2666-9145(22)00114-2
pmc: PMC9634033
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100225

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Auteurs

Volha V Malechka (VV)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Dat Duong (D)

Medical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.

Keyla D Bordonada (KD)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Amy Turriff (A)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Delphine Blain (D)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Elizabeth Murphy (E)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Wendy J Introne (WJ)

Medical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.
Human Biochemical Genetics Section, National Human Genome Research Institute, Bethesda, Maryland.

Bernadette R Gochuico (BR)

Medical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.
Human Biochemical Genetics Section, National Human Genome Research Institute, Bethesda, Maryland.

David R Adams (DR)

Medical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.
Human Biochemical Genetics Section, National Human Genome Research Institute, Bethesda, Maryland.

Wadih M Zein (WM)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Brian P Brooks (BP)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Laryssa A Huryn (LA)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Benjamin D Solomon (BD)

Medical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.

Robert B Hufnagel (RB)

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Classifications MeSH