SUMMARY OF KEY RESEARCH FINDINGS
The main risk factors for diabetic retinopathy are diabetes duration and poor glycaemic control. In this cross-sectional study, the authors aimed to assess the association between other metabolic risk factors and chronic inflammation with non-proliferative diabetic retinopathy in individuals with Type 1 diabetes in a large Finnish cohort. The authors presented preliminary results that have not yet undergone peer review in a full scientific publication. These preliminary results suggest that non-proliferative diabetic retinopathy is associated with higher high-sensitivity C-reactive protein concentrations even when accounting for other confounding factors. For metabolic syndrome, the results were less straightforward, but the odds of diabetic retinopathy increased with the number of metabolic syndrome components present. These preliminary findings suggest a potential role of chronic low-grade inflammation and the accumulation of several metabolic syndrome components in the early stage of diabetic retinopathy.1
WHAT CHALLENGE DOES THIS ADDRESS?
Diabetic retinopathy is one of the most prevalent complications of Type 1 diabetes.2 Several metabolic risk factors have been suggested to be associated with diabetic retinopathy, but the link between metabolic syndrome and diabetic retinopathy in Type 1 diabetes is still unclear.3 Metabolic syndrome is associated with chronic low-grade inflammation, which in turn is involved in the pathophysiological mechanisms underlying diabetic retinopathy. Yet, the link between markers of chronic low-grade inflammation and diabetic retinopathy in Type 1 diabetes remains uncertain,4,5 and there are very few studies that have investigated the risk factors associated with non-proliferative diabetic retinopathy, an early disease manifestation.
RELEVANCE TO EUROPEAN PRACTICE
The findings suggest that chronic low-grade inflammation is already associated with diabetic retinopathy at an early stage of the disease. In addition, the accumulation of multiple metabolic risk factors appears to be associated with non-proliferative diabetic retinopathy. As metabolic syndrome components and high-sensitivity C-reactive protein are readily assessable in clinical practice, they are potentially useful markers for risk stratification.6 However, further research is needed to establish causality and determine whether these factors play a direct role in the development of diabetic retinopathy in Type 1 diabetes.
WHAT ARE THE NEXT STEPS FOR THE RESEARCH?
As these findings are preliminary and derived from a cross-sectional study design, further research is required to determine whether high sensitivity C-reactive protein and/or metabolic syndrome are associated with diabetic retinopathy development or progression. Further follow-up analyses will investigate the risk of progression to proliferative diabetic retinopathy in Type 1 diabetes.






