Abstract

Purpose: This study aims to explore the correlations of arteriosclerosis-associated plasma indices with various severity levels of diabetic retinopathy (DR) and to test the hypothesis that elevated circulating level of known angiogenic cytokines induced by hyperglycemia is associated with dyslipidemia on DR.Methods: This cross-sectional study consists of 131 patients with type 2 diabetes. The patients were categorized based on their DR status into those with no DR (diabetes mellitus, DM), non-proliferative diabetic retinopathy (NPDR), and proliferative diabetic retinopathy (PDR) groups. The biochemical profile including fasting glucose, glycated hemoglobin (HbA1c), lipid profile were estimated, plasma angiogenic cytokines (vascular endothelial growth factor, VEGF-A, -C, -D) and placental growth factor (PlGF) were analyzed by protein microarrays. The atherogenic plasma index (API) was defined as low-density lipoprotein cholesterol/high-density lipoprotein cholesterol (LDL-C/HDL-C); atherogenic index (AI) was calculated as (TC-(HDL-C))/HDL-C and atherogenic index of plasma (AIP) was defined as log (TG/HDL-C).Results: No significant differences were detected in the duration of hypertension, age, and gender between the three groups. Serum TC and LDL-C, AI, and API in the NPDR group and PDR group were significantly higher than those in the DM group. The circulating level of PlGF, VEGF-A, and VEGF-C were significantly correlated with the severity of DR. VEGF-D is a risk factor independent of API (Z = −2.61, P = 0.009) and AI (Z = −2.40, P = 0.016). Multivariate logistic regression showed that AI and API are strong risk factors for the occurrence and severity of DR. Associated with AI and API, VEGF-D and PlGF contribute to DR: VEGF-D [AI: P = 0.038, odd ratio (OR) = 1.38; VEGF-D: P = 0.002, OR = 1.00. API: P = 0.027, OR = 1.56, VEGF-D:P = 0.002, OR = 1.00] and PlGF [AI: P = 0.021, OR = 1.43; VEGF-D: P = 0.004, OR = 1.50. API: P = 0.011, OR = 1.66; VEGF-D: P = 0.005, OR = 1.49].Conclusions: Total cholesterol (TC) and LDL-C are risk factors for presence of any DR. Atherogenic index and API are novel and better predictive indicators for the occurrence and severity of DR in comparion with the traditional lipid profiles. Abnormal lipid metabolism are associated with the upregulation of circulating cytokines that are linked to the severity of DR.

Highlights

  • Diabetic retinopathy (DR) is the most common ocular microvascular complication of diabetes mellitus (DM)

  • The fenofibrate intervention and event lowering in diabetes (FIELD) and the action to control cardiovascular risk in diabetes (ACCORD) studies demonstrated that abnormal lipid metabolism is associated with the onset and progression of DR but the underlying mechanisms are yet to be elucidated [3, 4]

  • We found that serum Total cholesterol (TC), low density lipoprotein (LDL)-C, atherogenic index (AI), and atherogenic plasma index (API) in the non-proliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR) groups were significantly higher than those in the DM group

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Summary

Introduction

Diabetic retinopathy (DR) is the most common ocular microvascular complication of diabetes mellitus (DM). Hyperglycemia is the strongest modifiable risk factor but people with optimal glycemic control develop DR. Ranibizumab and bevacizumab are VEGF-A inhibitors while aflibercept blocks VEGF-A and placental growth factor (PlGF). These anti-VEGF agents are superior to macular laser and a considerable proportion of patients improve visual acuity, the results of Diabetic Retinopathy Collaboration Network (DRCR.net) Protocol I and T studies show that persistent macular edema was seen in approximately 51–73% at 12 weeks and 32–66% after 24 weeks of regular anti-VEGF injections [5,6,7,8]

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