Association of vitreous vitamin C depletion with diabetic macular ischemia in proliferative diabetic retinopathy

PLoS One. 2019 Jun 19;14(6):e0218433. doi: 10.1371/journal.pone.0218433. eCollection 2019.

Abstract

Purpose: Vitreous vitamin C, as an anti-oxidant, is responsible for regulating oxygen tension and oxidative stress in the eye. Oxidative stress and retinal ischemia are implicated in the development of proliferative diabetic retinopathy (PDR). In this study, we aimed to determine whether vitreous level of vitamin C is compromised in patients with PDR and to investigate the association of diabetic macular ischemia and vitamin C.

Methods: This prospective study enrolled forty patients who underwent pars plana vitrectomy for the treatment of PDR (PDR group, n = 20) and idiopathic epiretinal membrane (control group, n = 20). Serum, aqueous humor, and the vitreous were collected for the analysis of vitamin C level by HPLC. Diabetic macular ischemia (DMI) in PDR group was evaluated with fluorescein angiography (FA).

Results: PDR patients (60.4 ± 2.1 y) were younger than non-diabetic control patients (67.4 ± 1.2 y). Serum, aqueous, and vitreous levels of vitamin C in PDR were 38.7%, 22.5%, and 11.1% of non-diabetic control group, respectively. All PDR patients had DMI (grade 1: 25%, grade 2: 30%, grade 3: 30%, grade 4: 15%). DMI grade was inversely correlated with the level of vitreous vitamin C (r = -0.546, P = 0.019), not with HbA1C, serum, or aqueous vitamin C level. In addition, the level of vitreous vitamin C (4.5 ± 2.6 μg/ml) in high DMI group (Gr 3 &4) was lower than that (31.0 ± 9.1 μg/ml) in low DMI group (Gr 1&2) (P = 0.015).

Conclusions: Vitreous level of vitamin C in PDR patients showed a tenfold decrease, which was associated with the degree of macular ischemia. This suggests that vitreous vitamin C depletion may cause macula ischemia in PDR patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antioxidants / therapeutic use*
  • Aqueous Humor / metabolism
  • Ascorbic Acid / metabolism*
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetes Mellitus, Type 2 / surgery
  • Diabetic Retinopathy / drug therapy*
  • Diabetic Retinopathy / pathology
  • Diabetic Retinopathy / surgery
  • Epiretinal Membrane / drug therapy
  • Epiretinal Membrane / pathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Oxidative Stress / drug effects
  • Vitrectomy
  • Vitreous Body / metabolism
  • Vitreous Body / pathology

Substances

  • Antioxidants
  • Ascorbic Acid

Grants and funding

This study was supported by the Yuhan corporation and Seoul National University Hospital (0620161840) to HGY. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.