Department of Experimental Medicine, Division of Pharmacology, University of Campania "Luigi Vanvitelli", Naples, Italy.
Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
Biochem Pharmacol. 2021 Apr;186:114473. doi: 10.1016/j.bcp.2021.114473. Epub 2021 Feb 16.
In this study we analyzed the expression of circulating miRNAs, in the serum of diabetic retinopathy (DR) patients. Five miRNAs (hsa-miR-195-5p, hsa-miR-20a-5p, hsa-miR-20b-5p, hsa-miR-27b-3p and hsa-miR-451a) were validated as biomarkers for stratification of DR stages, from the early non-proliferative (NPDR) to the late proliferative (PDR) phase. Furthermore, circulating levels of these miRNAs correlated with retinal hyper-reflective spots (HRS), assessed by optical coherence tomography (OCT). The number of HRS increased with worsening of DR stages. On the contrary, no significant vascular density differences between NPDR and PDR patients were detected by angio-OCT (OCTA). A post-hoc bioinformatics analysis associated these five miRNAs to target genes belonging to the "Tumor Necrosis Factor alfa signaling" pathway, and several molecules were predicted to modify miRNAs expression. In conclusion, correlation between specific circulating miRNAs and intraretinal hyper-reflective spots was demonstrated, confirming that these miRNAs were validated as prognostic biomarkers, and also as potential pharmacological targets, warranting further clinical evaluation to explore novel therapeutics for diabetic retinopathy.
在这项研究中,我们分析了糖尿病视网膜病变(DR)患者血清中循环 miRNA 的表达。验证了 5 个 miRNA(hsa-miR-195-5p、hsa-miR-20a-5p、hsa-miR-20b-5p、hsa-miR-27b-3p 和 hsa-miR-451a)可作为分层 DR 阶段的生物标志物,从早期非增生性(NPDR)到晚期增生性(PDR)阶段。此外,这些 miRNA 的循环水平与通过光学相干断层扫描(OCT)评估的视网膜高反射性斑点(HRS)相关。HRS 的数量随着 DR 阶段的恶化而增加。相反,血管造影 OCT(OCTA)未检测到 NPDR 和 PDR 患者之间血管密度的显著差异。事后生物信息学分析将这 5 个 miRNA 与属于“肿瘤坏死因子 alpha 信号”途径的靶基因相关联,并且预测了几种分子来修饰 miRNA 的表达。总之,特定循环 miRNA 与视网膜内高反射性斑点之间的相关性得到了证实,证实这些 miRNA 已被验证为预后生物标志物,并且也是潜在的药理学靶点,需要进一步的临床评估来探索糖尿病性视网膜病变的新疗法。