Mathur Priyanka, Rani Vibha
Department of Biotechnology, Transcriptome Laboratory, Centre for Emerging Diseases, Jaypee Institute of Information Technology, A-10, Sector-62, Noida-201307, U.P, India.
Curr Gene Ther. 2021;21(4):313-326. doi: 10.2174/1566523221666210311111619.
The risk of heart failure is 2-5 times higher in diabetic patients as compared to non-diabetic patients with similar comorbidities. Recent reports suggest that nearly half of the diabetic population remains undiagnosed, making diabetic cardiomyopathy (DCM) a clinically relevant entity. In the myocardium, chronic hyperglycemia elicits structural and functional abnormalities characterized by ventricular dilation, diastolic dysfunction, fibrosis, and hypertrophy leading to heart failure. Since diabetes is a multifactorial heterogeneous metabolic disorder which cannot be diagnosed or controlled along with coronary artery disease or hypertension, there is an urgent need to understand the underlying molecular mechanisms that leads to DCM and identify potential therapeutic targets. Small non-coding RNAs, in particular, microRNAs (miRNAs), have emerged as key regulators for several life-threatening diseases, including DCM. Recent studies have reported that miRNAs not only regulate the fundamental mechanisms of DCM such as insulin resistance, MAPK pathway, PI3K-AkT pathway, oxidative stress, also inflammatory signaling, but also possess the potential to be a therapeutic or diagnostic target. This review examines the role of critical miRNAs in the onset and pathogenesis of DCM, which also depicts high potential as therapeutic and diagnostic molecule in preclinical studies. Further, it highlights the completed and on-going clinical trials around the globe for diabetes and miRNAs to provide a outlook about the upcoming miRNA therapeutics.
与具有相似合并症的非糖尿病患者相比,糖尿病患者发生心力衰竭的风险要高出2至5倍。最近的报告表明,近一半的糖尿病患者仍未被诊断出来,这使得糖尿病性心肌病(DCM)成为一个具有临床相关性的病症。在心肌中,慢性高血糖会引发结构和功能异常,其特征为心室扩张、舒张功能障碍、纤维化和肥大,进而导致心力衰竭。由于糖尿病是一种多因素的异质性代谢紊乱疾病,无法与冠状动脉疾病或高血压一同被诊断或控制,因此迫切需要了解导致DCM的潜在分子机制,并确定潜在的治疗靶点。特别是小非编码RNA,尤其是微小RNA(miRNA),已成为包括DCM在内的几种危及生命疾病的关键调节因子。最近的研究报告称,miRNA不仅调节DCM的基本机制,如胰岛素抵抗、丝裂原活化蛋白激酶(MAPK)途径、磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-AkT)途径、氧化应激以及炎症信号传导,而且还具有成为治疗或诊断靶点的潜力。本综述探讨了关键miRNA在DCM发病和发病机制中的作用,这在临床前研究中也显示出作为治疗和诊断分子的巨大潜力。此外,它突出了全球范围内已完成和正在进行的关于糖尿病和miRNA的临床试验,以展望即将到来的miRNA治疗方法。