4.6 Article

Validating Variational Bayes Linear Regression Method With Multi-Central Datasets

Journal

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
Volume 59, Issue 5, Pages 1897-1904

Publisher

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.17-22907

Keywords

visual field; glaucoma; progression; variational Bayes; JAMDIG; The Japanese Archive of Multicentral Databases in Glaucoma; DIGS; the Diagnostic Innovations in Glaucoma Study

Categories

Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [17K11418, 17K16959]
  2. Japan Science, and Technology Agency (JST), CREST [JPMJCR1304]
  3. Daiichi Sankyo Foundation of Life Science
  4. National Eye Institute [EY011008, EY14267, EY019869, EY201818, P30EY022589]
  5. Grants-in-Aid for Scientific Research [17K11418, 17K11478, 17K16959] Funding Source: KAKEN

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PURPOSE. To validate the prediction accuracy of variational Bayes linear regression (VBLR) with two datasets external to the training dataset. METHOD. The training dataset consisted of 7268 eyes of 4278 subjects from the University of Tokyo Hospital. The Japanese Archive of Multicentral Databases in Glaucoma (JAMDIG) dataset consisted of 271 eyes of 177 patients, and the Diagnostic Innovations in Glaucoma Study (DIGS) dataset includes 248 eyes of 173 patients, which were used for validation. Prediction accuracy was compared between the VBLR and ordinary least squared linear regression (OLSLR). First, OLSLR and VBLR were carried out using total deviation (TD) values at each of the 52 test points from the second to fourth visual fields (VFs) (VF2-4) to 2nd to 10th VF (VF2-10) of each patient in JAMDIG and DIGS datasets, and the TD values of the 11th VF test were predicted every time. The predictive accuracy of each method was compared through the root mean squared error (RMSE) statistic. RESULTS. OLSLR RMSEs with the JAMDIG and DIGS datasets were between 31 and 4.3 dB, and between 19.5 and 3.9 dB. On the other hand, VBLR RMSEs with JAMDIG and DIGS datasets were between 5.0 and 3.7, and between 4.6 and 3.6 dB. There was statistically significant difference between VBLR and OLSLR for both datasets at every series (VF2-4 to VF2-10) (P < 0.01 for all tests). However, there was no statistically significant difference in VBLR RMSEs between JAMDIG and DIGS datasets at any series of VFs (VF2-2 to VF2-10) (P > 0.05). CONCLUSIONS. VBLR outperformed OLSLR to predict future VF progression, and the VBLR has a potential to be a helpful tool at clinical settings.

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