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Updated: Feb 4, 2026

In vivo Structural Assessments of Ocular Disease in Rodent Models using Optical Coherence Tomography
Published on: July 24, 2020
Progression of Diabetic Microaneurysms According to the Internal Reflectivity on Structural Optical Coherence
Mariacristina Parravano1, Daniele De Geronimo1, Fabio Scarinci1
1IRCCS - Fondazione Bietti, Rome, Italy.
Purpose:
To investigate the progression of diabetic microaneurysms (MAs) according to the spectral-domain optical coherence tomography (SD-OCT) and OCT angiography (OCTA) characteristics and to evaluate their influence on the retinal extracellular fluid accumulation at 1 year follow-up in patients with nonproliferative diabetic retinopathy (NPDR).
Design:
Prospective, observational case series.
Methods:
Fourteen patients with NPDR underwent SD-OCT and OCTA at the baseline and at 1 year follow-up. For all the selected MAs the visibility, the changes of internal reflectivity, graded as hyporeflective, moderate, or hyperreflective, and the extracellular fluid accumulation surrounding each MA on SD-OCT at 1 year were evaluated. The changes in terms of visualization at the level either of superficial (SCP) or deep (DCP) capillary plexus and the presence of flow on the corresponding OCTA scan at 1 year were evaluated.
Results:
Of 127 MAs selected at the baseline, 89 (70%) were still visible on SD-OCT at 1 year. The reflectivity pattern at baseline was strongly associated with extracellular fluid accumulation at 1 year, with 18% of hyporeflective vs 66% of hyperreflective MAs developing extracellular fluid (P = .004). Among OCTA findings, the presence of flow (P = .001), the visibility (P < .001), and the deep location (DCP or both DCP and SCP, P = .007) were strongly associated with the development of extracellular fluid at 12 months.
Conclusions:
This study suggests an association between the SD-OCT and OCTA characteristics of diabetic MAs and the retinal extracellular fluid accumulation at 1 year. A better interpretation of MA characteristics could improve the timing and the management of diabetic maculopathy.
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