OCT angiography may help detect glaucoma progression earlier than standard OCT or visual field exams, although its specificity was lower than that of structural OCT, according to data published in JAMA Ophthalmology.“Glaucoma progression is commonly monitored with structural OCT and visual field testing, but these tests do not always show progression at the same time,” Takashi Nishida, MD, PhD, associate project scientist at the Shiley Eye Institute, told Healio. “We conducted this study to compare when progression is detected by OCT-A, structural OCT and visual field
October 14, 2026
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OCT angiography may help detect glaucoma progression earlier than standard OCT or visual field exams, although its specificity was lower than that of structural OCT, according to data published in JAMA Ophthalmology.
“Glaucoma progression is commonly monitored with structural OCT and visual field testing, but these tests do not always show progression at the same time,” Takashi Nishida, MD, PhD, associate project scientist at the Shiley Eye Institute, told Healio. “We conducted this study to compare when progression is detected by OCT-A, structural OCT and visual field testing using event-based criteria and to determine whether OCT-A could provide an earlier signal of disease worsening.”
Nishida and colleagues retrospectively analyzed data on 180 eyes from 116 patients with glaucoma included in the Diagnostic Innovations in Glaucoma Study. They reviewed patient records to determine when they had crossed cutoff points of glaucoma progression on OCT, OCT-A and visual field tests with the Humphrey Field Analyzer II (Zeiss).
The cutoff point on OCT was 4.02 m of circumpapillary retinal nerve fiber layer thickness, and on OCT-A it was 4.1% circumpapillary capillary density. The cutoff for visual field progression was worsening pattern deviation in at least three identical test locations on three examinations vs. the average of two baseline tests.
“OCT and OCTA changes had to exceed established test-retest variability and be confirmed on two consecutive visits,” Nishida said. “We also evaluated specificity in clinically stable eyes, because earlier detection is useful only if it does not come with an excessive number of false-positive events.”
At least one modality detected progression in 107 eyes. The following showed glaucoma progression earliest:
“Among eyes that progressed by both modalities, OCT-A vessel density changes preceded visual field progression by an average of 2.3 years,” Nishida said, “while OCT [retinal nerve fiber layer] thinning preceded visual field progression by about 1.5 years.”
Different stages of glaucoma had different events that appeared first.
“[Retinal nerve fiber layer] thinning was more often the first signal in preperimetric glaucoma, while OCT-A vessel density loss was more often first in more established disease,” Nishida said.
The rates of false-positive events in the 45 stable eyes were 31.1% for OCT-A and 24.4% for OCT, from which the researchers calculated specificities of 68.9% and 75.6%, respectively.
The results “support a multimodal approach to glaucoma monitoring,” Nishida said.
“Different tests often identified progression in different eyes or at different times,” Nishida said. “This suggests that no single test captures all aspects of glaucomatous change.”
Nishida said OCT-A “may provide complementary information rather than replace OCT or visual field testing.”
“The main clinical message is that OCT-A may be particularly useful as an additional source of information when structural and functional tests are discordant,” Nishida said. “Further work is needed to standardize OCT-A progression criteria, address image artifacts and reproducibility and determine whether adding OCT-A to routine monitoring improves long-term patient outcomes enough to justify the additional testing.”
For more information:Takashi Nishida, MD, PhD, can be reached at tnishida@health.ucsd.edu.

While the role of OCT angiography continues to evolve, I have reservations about adopting it into glaucoma management in its current form. The authors present data on circumpapillary vessel density from a single platform, but this metric is not interchangeable across devices, and the progression threshold they used has no validated equivalent on other instruments. More fundamentally, “vessel density” on this instrument is a percentage derived from an en face projection of decorrelation signal within a segmented tissue volume, and it is unclear whether a decline in density reflects true vascular regression, altered flow distribution, vascular collapse, or simply a thresholding or segmentation artifact. The authors’ own specificity analysis reinforces this uncertainty; nearly one-third of clinically stable eyes met their OCT-A progression criteria. Practical considerations regarding OCT-A capture also give me pause. Its signal is highly sensitive to motion during capture and to media opacities, both common in glaucoma patients. Finally, as the authors acknowledge, their analysis relied on global (circumpapillary) metrics. Demonstrating regional vessel density loss that corresponds spatially to field defects would strengthen their case considerably. For now, I would view a decline in vessel density as a reason for closer surveillance rather than evidence of true progression.
Joe L. Wheat, OD, PhD, FAAO
Disclosures: Wheat reports no relevant financial disclosures.
Published by:
Hashemi M, et al. JAMA Ophthalmol. 2026;doi:10.1001/jamaophthalmol.2026.3545.
Disclosures: Nishida reports consulting for Topcon Healthcare outside this study. Please see the study for all other authors' relevant financial disclosures. The study was funded by grants from Akorn, Allergan, Merck, Novartis/Alcon Laboratories, Pfizer and Santen Pharmaceutical.
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