Zhang Jing-Yun, Gong Ying-Lan, Li Chun-Jun, Qi Qi, Zhang Qiu-Mei, Yu De-Min
Key Laboratory of Hormones and Development (Ministry of Health), Tianjin Key Laboratary of Metabolic Diseases, Tianjin Metabolic Diseases, Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University 300070, Tianjin, China.
Zhejiang University Zhejiang, China.
Am J Transl Res. 2016 Jun 15;8(6):2650-8. eCollection 2016.
Type 2 diabetes mellitus induced atherosclerosis (DA) is regarded as a major cause of disability and death in diabetic patients. The early prediction of atherosclerosis in patients DM is necessary. Therefore, we aimed to identify special plasma microRNAs that can serve as a novel non-invasive screening signature of DA patients with atherosclerosis and test its specificity and sensitivity in the early diagnosis of DA. In total, we obtained plasma samples from 285 diabetic atherosclerosis patients and matched diabetic retinopathy (DR) patients, diabetic nephropathy (DN) patients, diabetes mellitus without complication (DM) and healthy controls. An initial screening of miRNA expression was performed through TaqMan Low Density Array (TLDA). Three miRNAs were significantly increased in patients with DA compared with other groups after the multiple stages. The areas under the receiver operating characteristic (AUC) curves of the validated three-plasma miRNAs signature in DA comparing with NC were 0.881, 0.709 and 0.842 while the merged was 0.940 while DA comparing with DM was 0.879, 0.663, 0.731 and the merged was 0.928. The three miRNA could also distinguish DA from DN with an AUC of 0.894, 0.782, 0.910 and 0.963 (merged) as well as from DR with an AUC of 0.876, 0.815, 0.850 and 0.925 (merged). In conclusion, these data provide evidence that plasma miRNAs have the potential to be sensitive, cost-effective biomarkers for the early detection of DA. These biomarkers could serve as a dynamic monitoring factor for detecting the progression of DA from DR, DN, DM patients.
2型糖尿病诱发的动脉粥样硬化(DA)被认为是糖尿病患者致残和死亡的主要原因。对糖尿病患者的动脉粥样硬化进行早期预测很有必要。因此,我们旨在识别特殊的血浆微小RNA,其可作为DA型动脉粥样硬化患者的一种新型非侵入性筛查标志物,并测试其在DA早期诊断中的特异性和敏感性。我们总共从285例糖尿病性动脉粥样硬化患者以及匹配的糖尿病视网膜病变(DR)患者、糖尿病肾病(DN)患者、无并发症的糖尿病(DM)患者和健康对照者中获取了血浆样本。通过TaqMan低密度阵列(TLDA)对miRNA表达进行了初步筛查。经过多个阶段后,与其他组相比,DA患者中有三种miRNA显著增加。在DA中,经过验证的三种血浆miRNA标志物与正常对照相比,受试者工作特征(AUC)曲线下面积分别为0.881、0.709和0.842,合并后为0.940;与DM相比,AUC分别为0.879、0.663、0.731,合并后为0.928。这三种miRNA还能够区分DA与DN,AUC分别为0.894、0.782、0.910和0.963(合并),以及区分DA与DR,AUC分别为0.876、0.815、0.850和0.925(合并)。总之,这些数据证明血浆miRNA有潜力成为用于DA早期检测的敏感且经济高效的生物标志物。这些生物标志物可作为一种动态监测因素,用于检测DR、DN、DM患者中DA的进展情况。