AI Article Synopsis

  • * It involved 54 participants with diabetes and 48 controls undergoing various tests, revealing that those with diabetes had poorer contrast sensitivity and slowed response times in visual tasks.
  • * Findings indicated that while diabetics exhibited less circular foveal avascular zones, there were no significant differences in foveal vessel density, suggesting that functional impairments may not directly correlate with vascular changes in the retina.

Article Abstract

Purpose: This study measured associations between ON and OFF functional indicators and structural optical coherence tomography (OCT) and OCT angiography (OCTA) markers in diabetic retinal disease.

Methods: Fifty-four participants with type 1 or type 2 diabetes (mean age = 34.1 years; range 18-60) and 48 age-matched controls (mean age = 35.4 years, range 18-59) underwent visual psychophysical testing, OCT and OCTA retinal imaging. Psychophysical tasks measuring (A) contrast increment and decrement sensitivity and (B) response times to increment and decrement targets were assessed as surrogate measures of ON and OFF retinal ganglion cell function.

Results: The group with diabetes had worse foveal contrast increment and decrement thresholds (p = 0.04) and were slower to search for increment and decrement targets relative to controls (p = 0.009). Individuals with diabetes had a less circular foveal avascular zone (FAZ) (p < 0.001) but did not differ from controls in foveal vessel density and FAZ area. Functional and structural outcome measures related to the peripheral retina were also comparable between those with and without diabetes. Functional responses to increments and decrements were not significantly correlated with FAZ circularity or vessel density in individuals with diabetes.

Conclusions: Diabetic retinal disease results in impaired performance on measures of inferred ON and OFF pathway function in addition to vascular deficits measurable with OCTA. Future longitudinal studies may determine the temporal relationship between these deficits, and whether they predict future diabetic retinopathy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629852PMC
http://dx.doi.org/10.1111/opo.13394DOI Listing

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