Lipids and Atherosclerosis Unit, Reina Sofıa University Hospital, Córdoba, Spain.
IMIBIC/Reina Sofía University Hospital, University of Córdoba and CIBER Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
Exp Mol Med. 2018 Dec 26;50(12):1-12. doi: 10.1038/s12276-018-0194-y.
We aimed to explore whether changes in circulating levels of miRNAs according to type 2 diabetes mellitus (T2DM) or prediabetes status could be used as biomarkers to evaluate the risk of developing the disease. The study included 462 patients without T2DM at baseline from the CORDIOPREV trial. After a median follow-up of 60 months, 107 of the subjects developed T2DM, 30 developed prediabetes, 223 maintained prediabetes and 78 remained disease-free. Plasma levels of four miRNAs related to insulin signaling and beta-cell function were measured by RT-PCR. We analyzed the relationship between miRNAs levels and insulin signaling and release indexes at baseline and after the follow-up period. The risk of developing disease based on tertiles (T1-T2-T3) of baseline miRNAs levels was evaluated by COX analysis. Thus, we observed higher miR-150 and miR-30a-5p and lower miR-15a and miR-375 baseline levels in subjects with T2DM than in disease-free subjects. Patients with high miR-150 and miR-30a-5p baseline levels had lower disposition index (p = 0.047 and p = 0.007, respectively). The higher risk of disease was associated with high levels (T3) of miR-150 and miR-30a-5p (HR = 4.218 and HR = 2.527, respectively) and low levels (T1) of miR-15a and miR-375 (HR = 3.269 and HR = 1.604, respectively). In conclusion, our study showed that deregulated plasma levels of miR-150, miR-30a-5p, miR-15a, and miR-375 were observed years before the onset of T2DM and pre-DM and could be used to evaluate the risk of developing the disease, which may improve prediction and prevention among individuals at high risk for T2DM.
我们旨在探索根据 2 型糖尿病(T2DM)或糖尿病前期状态改变循环 miRNA 水平是否可作为评估发病风险的生物标志物。本研究纳入了 CORDIOPREV 试验中基线时无 T2DM 的 462 例患者。中位随访 60 个月后,107 例患者发生 T2DM,30 例发生糖尿病前期,223 例维持糖尿病前期,78 例无疾病。通过 RT-PCR 测定与胰岛素信号和β细胞功能相关的四种 miRNA 的血浆水平。我们分析了基线和随访后 miRNA 水平与胰岛素信号和释放指数之间的关系。通过 COX 分析评估基于基线 miRNA 水平三分位(T1-T2-T3)的发病风险。因此,我们观察到 T2DM 患者的 miR-150 和 miR-30a-5p 基础水平较高,miR-15a 和 miR-375 基础水平较低。miR-150 和 miR-30a-5p 基础水平较高的患者,其处置指数较低(分别为 p=0.047 和 p=0.007)。高 miR-150 和 miR-30a-5p 水平与疾病风险增加相关(HR=4.218 和 HR=2.527),而 miR-15a 和 miR-375 水平较低(HR=3.269 和 HR=1.604)。总之,我们的研究表明,miR-150、miR-30a-5p、miR-15a 和 miR-375 的循环水平失调可在 T2DM 和糖尿病前期发病前数年观察到,可用于评估发病风险,这可能有助于改善高危个体的预测和预防。