Relationship of skin autofluorescence to severity of retinopathy in type 2 diabetes

Curr Eye Res. 2015 Mar;40(3):338-45. doi: 10.3109/02713683.2014.918152. Epub 2014 May 28.

Abstract

Purpose: To evaluate the relationship between skin autofluorescence (SAF), which reflects the accumulation of advanced glycation end products (AGEs), and the severity of diabetic retinopathy (DR) in patients with type 2 diabetes.

Methods: Sixty-seven eyes of 67 patients with type 2 diabetes were enrolled. Sixty-seven age-matched non-diabetic subjects served as controls. Diabetic patients were classified by the severity of their DR: no DR (NDR), non-proliferative DR (NPDR), and proliferative DR (PDR). SAF was measured with an autofluorescence reader.

Results: SAF in the diabetes patients was significantly higher than in the controls (median 2.5 (interquartile range 2.3-2.7) and 1.8 (1.6-2.3) arbitrary unit (AU), respectively, p < 0.001). There was a statistically significant increase in SAF along with the increasing severity of DR (from NDR to NPDR: p = 0.034; NPDR to PDR: p < 0.01). Logistic regression analysis revealed that SAF (OR, 17.2; p < 0.05) was an independent factor indicating the presence of PDR.

Conclusions: SAF has an independent relationship with PDR in patients with type 2 diabetes. SAF measurement with an autofluorescence reader is a non-invasive way to assess the risk of DR. SAF may, therefore, be a surrogate marker candidate for the non-invasive evaluation of DR.

Keywords: AGE; Advanced glycation end products; biomarker; diabetic retinopathy; skin autofluorescence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Biomarkers / metabolism*
  • Blood Pressure
  • Body Mass Index
  • Case-Control Studies
  • Creatinine / blood
  • Diabetes Mellitus, Type 2 / diagnosis
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetic Retinopathy / diagnosis
  • Diabetic Retinopathy / metabolism*
  • Female
  • Glycation End Products, Advanced / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Optical Imaging*
  • Risk Assessment
  • Severity of Illness Index
  • Skin / metabolism*

Substances

  • Biomarkers
  • Glycation End Products, Advanced
  • Creatinine