Fig. 2.

Retinal blood flow and tissue volume of the inner retina. a. A representative image of the retina from an AD patient was imaged using the RFI with a FOV of 4.3 × 4.3 mm² (20-degrees setting) centered on the fovea, corresponding to the dark area in the center. The blood flow velocities (mm/s) were overlaid with the vessels. The arterioles marked in red have negative velocity values, indicating that blood is flowing away from the heart (flow moving towards the fovea). The venules marked in purple have positive velocity values, indicating that blood is flowing towards the heart. To analyze the blood flow in the macula, a 2.5 mm circle (blue) centered on the fovea was outlined. Vessel diameters of the vessels crossing the circle were measured at the locations marked as yellow and green dots. The arteriolar blood flow of these arterioles was calculated using the velocity and diameter (yellow dot). The venular blood flow of these venules was also calculated using velocity and diameter (green dot). All the flow measurements in the arterioles (all yellow dots) were summed to obtain the total arteriolar flow of the macula. Similarly, all the flow measurements in the venules (all green dots) were summed to obtain the total venular flow of the macula. b. To measure the tissue volume, the same eye was imaged using a custom UHR-OCT with a raster scan of 6 × 6 mm². To calculate the tissue-dependent blood perfusion, volumetric tissue volume of the inner retina, including RFNL, GCIPL, INL and OPL was measured using segmentation software (Orion, Voxeleron) in the round area with a diameter of 2.5 mm centered on the fovea. RNFL: retinal nerve fiber layer; GCIPL: ganglion cell-inner plexiform layer; INL: inner nuclear layer; OPL: outer plexiform layer; ONL: outer nuclear layer; and PR: retinal photoreceptor