Barutta Federica, Bruno Graziella, Matullo Giuseppe, Chaturvedi Nish, Grimaldi Serena, Schalkwijk Casper, Stehouwer Coen D, Fuller John H, Gruden Gabriella
Diabetic Nephropathy Laboratory, Department of Medical Sciences, University of Turin, C/so Dogliotti 14, 10126, Turin, Italy.
Human Genetics Foundation (HuGeF), Turin, Italy.
Acta Diabetol. 2017 Feb;54(2):133-139. doi: 10.1007/s00592-016-0915-4. Epub 2016 Oct 1.
Increasing evidence suggests a potential role of circulating miRNAs as clinical biomarkers, and loss of miRNA-126 has been proposed as a predictor of type 2 diabetes onset. However, a systematic analysis of circulating miRNAs in type 1 diabetic patients with micro-/macrovascular complications has not yet been performed.
A cross-sectional nested case-control study from the EURODIAB Prospective Complications Study of 455 type 1 diabetic patients was performed. Case subjects (n = 312) were defined as those with one or more complications of diabetes; control subjects (n = 143) were those with no evidence of any complication. A differential miRNA expression profiling was performed in pooled serum samples from cases and controls. Furthermore, miR-126 levels were quantified by qPCR in all individual samples and associations with diabetic complications investigated.
Twenty-five miRNAs differed in pooled samples from cases and controls. miR-126 levels were significantly lower in case than in control subjects, even after adjustment for age and sex. In logistic regression analyses, miR-126 was negatively associated with all complications (OR = 0.85, 95 % CI 0.75-0.96) as well as with each micro-/macrovascular complication examined separately. This was likely dependent of diabetes as associations were no longer significant after adjustment for both hyperglycemia and diabetes duration. However, a significant 25 % risk reduction, independent of age, sex, A1C, and diabetes duration, was still observed for proliferative retinopathy (OR = 0.75, 95 % CI 0.59-0.95).
In this large cohort of type 1 diabetic subjects, we found that miR-126 levels are associated with vascular complications of diabetes, particularly with proliferative retinopathy.
越来越多的证据表明循环miRNA作为临床生物标志物具有潜在作用,并且有人提出miRNA - 126的缺失是2型糖尿病发病的预测指标。然而,尚未对患有微血管/大血管并发症的1型糖尿病患者的循环miRNA进行系统分析。
对欧洲糖尿病前瞻性并发症研究中的455例1型糖尿病患者进行了一项横断面巢式病例对照研究。病例组(n = 312)定义为患有一种或多种糖尿病并发症的患者;对照组(n = 143)为没有任何并发症迹象的患者。对病例组和对照组的混合血清样本进行差异miRNA表达谱分析。此外,通过qPCR对所有个体样本中的miR - 126水平进行定量,并研究其与糖尿病并发症的关联。
病例组和对照组的混合样本中有25种miRNA存在差异。即使在调整年龄和性别后,病例组中miR - 126水平仍显著低于对照组。在逻辑回归分析中,miR - 126与所有并发症(OR = 0.85,95%CI 0.75 - 0.96)以及分别检查的每种微血管/大血管并发症均呈负相关。这可能与糖尿病有关,因为在调整高血糖和糖尿病病程后,这种关联不再显著。然而,对于增殖性视网膜病变,仍观察到独立于年龄、性别、糖化血红蛋白(A1C)和糖尿病病程的25%的显著风险降低(OR = 0.75,95%CI 0.59 - 0.95)。
在这个大型的1型糖尿病患者队列中,我们发现miR - 126水平与糖尿病血管并发症相关,特别是与增殖性视网膜病变相关。