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Deep Learning Approaches for Detecting of Nascent Geographic Atrophy in Age-Related Macular Degeneration.
Yao, Heming; Wu, Zhichao; Gao, Simon S; Guymer, Robyn H; Steffen, Verena; Chen, Hao; Hejrati, Mohsen; Zhang, Miao.
Afiliación
  • Yao H; gRED Computational Science, Genentech, Inc., South San Francisco, California.
  • Wu Z; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Gao SS; Ophthalmology Division, Department of Surgery, The University of Melbourne, Melbourne, Victoria, Australia.
  • Guymer RH; gRED Computational Science, Genentech, Inc., South San Francisco, California.
  • Steffen V; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Chen H; Ophthalmology Division, Department of Surgery, The University of Melbourne, Melbourne, Victoria, Australia.
  • Hejrati M; gRED Computational Science, Genentech, Inc., South San Francisco, California.
  • Zhang M; gRED Computational Science, Genentech, Inc., South San Francisco, California.
Ophthalmol Sci ; 4(3): 100428, 2024.
Article en En | MEDLINE | ID: mdl-38284101
ABSTRACT

Purpose:

Nascent geographic atrophy (nGA) refers to specific features seen on OCT B-scans, which are strongly associated with the future development of geographic atrophy (GA). This study sought to develop a deep learning model to screen OCT B-scans for nGA that warrant further manual review (an artificial intelligence [AI]-assisted approach), and to determine the extent of reduction in OCT B-scan load requiring manual review while maintaining near-perfect nGA detection performance.

Design:

Development and evaluation of a deep learning model.

Participants:

One thousand eight hundred and eighty four OCT volume scans (49 B-scans per volume) without neovascular age-related macular degeneration from 280 eyes of 140 participants with bilateral large drusen at baseline, seen at 6-monthly intervals up to a 36-month period (from which 40 eyes developed nGA).

Methods:

OCT volume and B-scans were labeled for the presence of nGA. Their presence at the volume scan level provided the ground truth for training a deep learning model to identify OCT B-scans that potentially showed nGA requiring manual review. Using a threshold that provided a sensitivity of 0.99, the B-scans identified were assigned the ground truth label with the AI-assisted approach. The performance of this approach for detecting nGA across all visits, or at the visit of nGA onset, was evaluated using fivefold cross-validation. Main Outcome

Measures:

Sensitivity for detecting nGA, and proportion of OCT B-scans requiring manual review.

Results:

The AI-assisted approach (utilizing outputs from the deep learning model to guide manual review) had a sensitivity of 0.97 (95% confidence interval [CI] = 0.93-1.00) and 0.95 (95% CI = 0.87-1.00) for detecting nGA across all visits and at the visit of nGA onset, respectively, when requiring manual review of only 2.7% and 1.9% of selected OCT B-scans, respectively.

Conclusions:

A deep learning model could be used to enable near-perfect detection of nGA onset while reducing the number of OCT B-scans requiring manual review by over 50-fold. This AI-assisted approach shows promise for substantially reducing the current burden of manual review of OCT B-scans to detect this crucial feature that portends future development of GA. Financial Disclosures Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Ophthalmol Sci Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Ophthalmol Sci Año: 2024 Tipo del documento: Article