Abstract
Aim A cross-sectional study was performed to examine the alterations of the retinal pigment epithelium– (RPE–) photoreceptor complex layer in type 2 diabetes mellitus (DM) without diabetic retinopathy (DR), using spectral-domain optical coherence tomography (SD-OCT). Methods Patients with type 2 DM without DR and healthy controls without DM were recruited. All participants underwent examinations including SD-OCT. The thickness measurements of the retinal neural layers were calculated after automatic segmentation. An independent-sample t-test was used to compare the means of the thickness of retinal neural layers in patients with DM and healthy controls. Results Sixty-seven eyes from 67 patients with DM and 30 eyes from 30 healthy controls were included in this study. No significant differences were found in age (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (P = 0.601), gender (Conclusion Lesions in the RPE–photoreceptor complex are present without vascular abnormalities, which may precede the alterations of ganglion cells in patients with type 2 DM.
Highlights
Diabetic retinopathy (DR) caused by type 2 diabetes mellitus (DM) is one of the major complications leading to blindness
Sixty-seven eyes from 67 patients with type 2 DM without DR were included in the DM group, and 30 eyes from 30 healthy controls were recruited in the control group
We reported an increase in the thickness of the retinal pigment epithelium (RPE)–photoreceptor complex in the macula of diabetic eyes without any sign of DR
Summary
Diabetic retinopathy (DR) caused by type 2 diabetes mellitus (DM) is one of the major complications leading to blindness. Investigators began to explore the changes in OCT images to verify the presence of early neural dysfunction. They discovered the damages of the retinal nerve fiber layer (RNFL) and ganglion cell– inner plexiform layer or ganglion cell layer (GCL) [6,7,8]. Some other studies [9,10,11,12] have focused on the outer layers of the retina, such as the outer nuclear layer (ONL), inner segment photoreceptors, or outer segment photoreceptors (OS).
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