Purpose
AMD degrades reading vision in aged persons worldwide. Hyper-transmission defects (HTDs) on optical coherence tomography (OCT), a structural clinical imaging biomarker for AMD progression, represents loss of shadowing by degenerating retinal pigment epithelium (RPE). We sought HTDs in individuals with normal eyes, early AMD (eAMD), and intermediate AMD (iAMD).
Methods
One eye of each participant in the baseline visit of the Alabama Study on Early Age-Related Macular Degeneration 2 (ALSTAR2) was analyzed. AMD presence and severity was determined using standardized color fundus photography. Participants underwent volume OCT angiography imaging. HTDs were defined in en face scans by hyper-intensity of signal in the choroid, confirmed on B-scans by the presence of RPE disruption, and measured by fitting circles.
Results
In 460 eyes of 460 participants (normal N=236, eAMD N=134, iAMD N=90), HTDs were detected in 134. Prevalence of any HTD (minimum diameter ≥62 μm) was higher in eyes with iAMD (86.7%, N=78) and eAMD (35.1%, N=47) compared to normal eyes (3.8%, N=9). Prevalence of HTD ≥250 μm was higher in eyes with iAMD (13.3%, N=12) and eAMD (5.2%, N=7) compared to normal eyes (0.4%, N=1).
Conclusions
More and larger HTDs are found in later stages of AMD. Degeneration of the RPE layer leads to HTDs and can be quickly identified on face OCTA scans. Persistent HTDs are markers for geography atrophy, an AMD end-stage (PMID 36958537). The prognostic significance of HTD identified at early stages of AMD will be clarified by imaging of the same participants at 3-year follow-up.