AI Article Synopsis

  • Myopic choroidal neovascularization (mCNV) is a major cause of vision loss in pathological myopia, making visual prognosis prediction difficult.
  • A study developed two AI models to predict visual acuity (VA) in 279 patients with mCNV, using horizontal/vertical OCT images and multiple-volume scans, achieving high accuracy in predictions over 1 to 3 years.
  • The findings suggest that incorporating OCT images and baseline VA data significantly improves prediction performance, which could help in assessing treatment outcomes for mCNV patients receiving anti-VEGF therapy.

Article Abstract

Myopic choroidal neovascularization (mCNV) is a common cause of vision loss in patients with pathological myopia. However, predicting the visual prognosis of patients with mCNV remains challenging. This study aimed to develop an artificial intelligence (AI) model to predict visual acuity (VA) in patients with mCNV. This study included 279 patients with mCNV at baseline; patient data were collected, including optical coherence tomography (OCT) images, VA, and demographic information. Two models were developed: one comprising horizontal/vertical OCT images (H/V cuts) and the second comprising 25 volume scan images. The coefficient of determination (R) and root mean square error (RMSE) were computed to evaluate the performance of the trained network. The models achieved high performance in predicting VA after 1 (R = 0.911, RMSE = 0.151), 2 (R = 0.894, RMSE = 0.254), and 3 (R = 0.891, RMSE = 0.227) years. Using multiple-volume scanning, OCT images enhanced the performance of the models relative to using only H/V cuts. This study proposes AI models to predict VA in patients with mCNV. The models achieved high performance by incorporating the baseline VA, OCT images, and post-injection data. This model could assist in predicting the visual prognosis and evaluating treatment outcomes in patients with mCNV undergoing intravitreal anti-vascular endothelial growth factor therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452208PMC
http://dx.doi.org/10.3390/biomedicines11082238DOI Listing

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