Shakthiya T, Chand Leena, Annamalai Radha, K A Arul Senghor
Biochemistry, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Ophthalmology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Cureus. 2024 Aug 31;16(8):e68273. doi: 10.7759/cureus.68273. eCollection 2024 Aug.
Introduction Diabetic retinopathy (DR) is a microvascular ailment that can arise from the long-term effects of diabetes mellitus. It can potentially cause retinal damage that could endanger vision and cause blindness. The worsening of DR is mainly linked to poor glycemic control, uncontrolled hypertension, and dyslipidemia. There is a need for alternative and clinically significant novel molecules involved in the pathogenesis of DR because the diagnostic and prognostic markers have reached a limit. Materials and method This study included sex and age-matched diabetic patients with proliferative stage (N = 70), non-proliferative stage (N = 80), and control (N = 80, without the sign of DR). These patients were recruited from outpatients in the Department of Ophthalmology, Sri Ramachandra Institute of Higher Education and Research, Chennai, India. A random blood sample was collected from each study participant, and the serum was separated after centrifugation and stored at -80 °C for batch analysis. The biomarkers vascular endothelial growth factor (VEGF-A) and angiopoietin-like protein-2 (ANGPTL2) were measured using a sandwich enzyme-linked immunosorbent assay (ELISA) technique, and the laboratory parameters such as fasting blood sugar (FBS), lipid profile, blood urea nitrogen (BUN), creatine, and glycated hemoglobin (HbA1C) were also assessed. Results We observed statistically significant differences in the duration of diabetes, FBS, total cholesterol (TC), triglyceride level (TGL), BUN, and creatine (p<0.05), and the mean age of study participants was 52.95±8.20 years in the control group, 53.85±10.20 years in the proliferative diabetic retinopathy (PDR) group, and 55.02±7.65 in the non-proliferative diabetic retinopathy (NPDR) group. Furthermore, ANGPTL2 levels were statistically significant according to the severity of the disease (p<0.001*), and they were also linked (p<0.05) with established markers such as VEGF-A. Conclusion Thus, our research implies that the up-regulated markers might be linked to the disease's advancement and could serve as a prognostic indicator or therapeutic target for DR.
引言
糖尿病性视网膜病变(DR)是一种微血管疾病,可由糖尿病的长期影响引发。它可能导致视网膜损伤,危及视力并导致失明。DR的恶化主要与血糖控制不佳、高血压未得到控制以及血脂异常有关。由于诊断和预后标志物已达到极限,因此需要参与DR发病机制的替代性且具有临床意义的新分子。
材料与方法
本研究纳入了年龄和性别匹配的糖尿病患者,其中增殖期患者70例,非增殖期患者80例,对照组80例(无DR迹象)。这些患者来自印度钦奈斯里兰卡拉马钱德拉高等教育与研究学院眼科门诊。从每位研究参与者采集随机血样,离心后分离血清并储存在-80°C以备批量分析。使用夹心酶联免疫吸附测定(ELISA)技术检测生物标志物血管内皮生长因子(VEGF-A)和血管生成素样蛋白2(ANGPTL2),并评估空腹血糖(FBS)、血脂谱、血尿素氮(BUN)、肌酐和糖化血红蛋白(HbA1C)等实验室参数。
结果
我们观察到糖尿病病程、FBS、总胆固醇(TC)、甘油三酯水平(TGL)、BUN和肌酐存在统计学显著差异(p<0.05),研究参与者的平均年龄在对照组为52.95±8.20岁,增殖性糖尿病性视网膜病变(PDR)组为53.85±10.20岁,非增殖性糖尿病性视网膜病变(NPDR)组为55.02±7.65岁。此外根据疾病严重程度,ANGPTL2水平具有统计学显著性(p<0.001*),并且它们还与VEGF-A等既定标志物相关(p<0.05)。
结论
因此,我们的研究表明上调的标志物可能与疾病进展相关,并且可以作为DR的预后指标或治疗靶点。