Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland
Department of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
BMJ Open Diabetes Res Care. 2020 Nov;8(2). doi: 10.1136/bmjdrc-2020-001379.
Patients with the ultra-rare Wolfram syndrome (WFS) develop insulin-dependent diabetes and progressive neurodegeneration. The aim of the study was to quantify microRNAs (miRNAs) in sera from patients with WFS, correlate their expression with neurological imaging over time and compare miRNA levels with those observed in patients with type 1 diabetes mellitus (T1DM).
We quantified miRNA expression (Qiagen, Germany) in two groups of patients: with WFS at study entry (n=14) and after 2 years of follow-up and in 15 glycated hemoglobin-matched (p=0.72) patients with T1DM.
We observed dynamic changes in the expression of multiple miRNAs in patients with WFS parallel to disease progression and in comparison to the T1DM patients group. Among miRNAs that differed between baseline and follow-up WFS samples, the level of 5 increased over time (miR-375, miR-30d-5p, miR-30e-30, miR-145-5p and miR-193a-5p) and was inversely correlated with macular average thickness, while the expression of 2 (let-7g-5p and miR-22-3p) decreased and was directly correlated with neuroimaging indicators of neurodegeneration.
Our findings show for the first time that serum miRNAs can be used as easily accessible indicators of disease progression in patients with WFS, potentially facilitating clinical trials on mitigating neurodegeneration.
患有超罕见的 WFS(Wolfram 综合征)的患者会出现胰岛素依赖型糖尿病和进行性神经退行性病变。本研究旨在定量分析 WFS 患者血清中的 microRNAs(miRNAs),并随时间推移将其表达与神经影像学相关联,同时将 miRNA 水平与 1 型糖尿病患者(T1DM)进行比较。
我们使用 Qiagen(德国)定量分析了两组患者的 miRNA 表达:研究入组时的 WFS 患者(n=14)和随访 2 年后的 WFS 患者,以及 15 名糖化血红蛋白匹配的 T1DM 患者(p=0.72)。
我们观察到 WFS 患者的 miRNA 表达随疾病进展呈动态变化,并与 T1DM 患者组进行比较。在基线和随访的 WFS 样本之间存在差异的 miRNA 中,5 种 miRNA 的水平随时间增加(miR-375、miR-30d-5p、miR-30e-30、miR-145-5p 和 miR-193a-5p),且与黄斑平均厚度呈负相关,而 2 种 miRNA(let-7g-5p 和 miR-22-3p)的表达降低,与神经影像学的神经退行性病变指标呈正相关。
我们的研究结果首次表明,血清 miRNA 可作为 WFS 患者疾病进展的易获取指标,这可能有助于进行减轻神经退行性病变的临床试验。