4.4 Article

Retinal venular oxygen saturation is associated with non-proliferative diabetic retinopathy in young patients with type 1 diabetes

期刊

ACTA OPHTHALMOLOGICA
卷 100, 期 4, 页码 388-394

出版社

WILEY
DOI: 10.1111/aos.15018

关键词

retinal oximetry; retinal vessel oxygen saturation; diabetic retinopathy; type 1 diabetes; retinal vessel calibres; retinal microvasculature; OCT angiography

资金

  1. South-Eastern Norway Regional Health Authority
  2. Norwegian Association of the Blind and Partially Sighted
  3. Dam Foundation
  4. Norwegian Diabetes Association

向作者/读者索取更多资源

The study aimed to investigate the role of retinal vessel density, central retinal vessel diameter, and retinal oxygen saturation in the development of non-proliferative diabetic retinopathy. Results showed that age and AV-O2 saturation difference were significantly associated with NPDR.
Purpose To determine the contribution of retinal vessel density (VD), central retinal vessel diameter and retinal oxygen (O-2) saturation independently of other known risk factors in the development of non-proliferative diabetic retinopathy (NPDR). Methods Macular optical coherence tomography angiography (OCTA), central retinal artery/vein equivalent diameter (CRAE/CRVE) measurements and retinal oximetry were performed in a cross-sectional study of 166 eyes from 166 individuals with type 1 diabetes (T1D) aged 14-30 years. Multiple logistic regression analysis was used to investigate whether O-2 saturation, retinal vessel diameters and vessel density in the deep capillary plexus (VD-DCP) were associated with NPDR, when adjusting for known risk factors. The individuals were allocated to one group without and one group with NPDR. Results Multiple logistic regression analysis showed that age (OR = 1.25, 95% CI: 1.04-1.49) and AV-difference in O-2 saturation (OR = 0.85, 95% CI 0.77-0.93) were significantly associated with NPDR. Conclusion Our findings suggest that age and lower AV-O-2 saturation difference contribute to explaining the grade of NPDR independently of other well-known risk factors. Reduced delivery of O-2 to the retinal tissue is associated with the development of NPDR in young patients with T1D and should be given appropriate weight in the risk stratification at early stages of the disease.

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