Prediction of anti-vascular endothelial growth factor agent-specific treatment outcomes in neovascular age-related macular degeneration using a generative adversarial network
Scientific Reports, ISSN: 2045-2322, Vol: 13, Issue: 1, Page: 5639
2023
- 19Citations
- 46Captures
- 1Mentions
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Metrics Details
- Citations19
- Citation Indexes19
- 19
- Captures46
- Readers46
- 46
- Mentions1
- News Mentions1
- 1
Most Recent News
Researchers from School of Electrical Engineering and Computer Science Describe Findings in Personalized Medicine (Prediction of anti-vascular endothelial growth factor agent-specific treatment outcomes in neovascular age-related macular ...)
2023 APR 20 (NewsRx) -- By a News Reporter-Staff News Editor at Angiogenesis Daily -- Data detailed on personalized medicine have been presented. According to
Article Description
To develop an artificial intelligence (AI) model that predicts anti-vascular endothelial growth factor (VEGF) agent-specific anatomical treatment outcomes in neovascular age-related macular degeneration (AMD), thereby assisting clinicians in selecting the most suitable anti-VEGF agent for each patient. This retrospective study included patients diagnosed with neovascular AMD who received three loading injections of either ranibizumab or aflibercept. Training was performed using optical coherence tomography (OCT) images with an attention generative adversarial network (GAN) model. To test the performance of the AI model, the sensitivity and specificity to predict the presence of retinal fluid after treatment were calculated for the AI model, an experienced (Examiner 1), and a less experienced (Examiner 2) human examiners. A total of 1684 OCT images from 842 patients (419 treated with ranibizumab and 423 treated with aflibercept) were used as the training set. Testing was performed using images from 98 patients. In patients treated with ranibizumab, the sensitivity and specificity, respectively, were 0.615 and 0.667 for the AI model, 0.385 and 0.861 for Examiner 1, and 0.231 and 0.806 for Examiner 2. In patients treated with aflibercept, the sensitivity and specificity, respectively, were 0.857 and 0.881 for the AI model, 0.429 and 0.976 for Examiner 1, and 0.429 and 0.857 for Examiner 2. In 18.5% of cases, the fluid status of synthetic posttreatment images differed between ranibizumab and aflibercept. The AI model using GAN might predict anti-VEGF agent-specific short-term treatment outcomes with relatively higher sensitivity than human examiners. Additionally, there was a difference in the efficacy in fluid resolution between the anti-VEGF agents. These results suggest the potential of AI in personalized medicine for patients with neovascular AMD.
Bibliographic Details
Springer Science and Business Media LLC
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