Institute for Molecular Cardiovascular Research (IMCAR), RWTH Aachen University Hospital, 52074 Aachen, Germany.
Department of Pathology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Centre, 6229 ER Maastricht, The Netherlands.
Int J Mol Sci. 2020 Sep 7;21(18):6547. doi: 10.3390/ijms21186547.
There are still major challenges regarding the early diagnosis and treatment of chronic kidney disease (CKD), which is in part due to the fact that its pathophysiology is very complex and not clarified in detail. The diagnosis of CKD commonly is made after kidney damage has occurred. This highlights the need for better mechanistic insight into CKD as well as improved clinical tools for both diagnosis and treatment. In the last decade, many studies have focused on microRNAs (miRs) as novel diagnostic tools or clinical targets. MiRs are small non-coding RNA molecules that are involved in post-transcriptional gene regulation and many have been studied in CKD. A wide array of pre-clinical and clinical studies have highlighted the potential role for miRs in the pathogenesis of hypertensive nephropathy, diabetic nephropathy, glomerulonephritis, kidney tubulointerstitial fibrosis, and some of the associated cardiovascular complications. In this review, we will provide an overview of the miRs studied in CKD, especially highlighting miR-103a-3p, miR-192-5p, the miR-29 family and miR-21-5p as these have the greatest potential to result in novel therapeutic and diagnostic strategies.
慢性肾脏病(CKD)的早期诊断和治疗仍然存在重大挑战,部分原因是其病理生理学非常复杂,尚未详细阐明。CKD 的诊断通常是在肾脏损伤发生后做出的。这凸显了需要更好地了解 CKD 的发病机制,以及改进用于诊断和治疗的临床工具。在过去十年中,许多研究都集中在 microRNAs(miRs)作为新型诊断工具或临床靶点上。miRs 是参与转录后基因调控的小非编码 RNA 分子,许多在 CKD 中都有研究。大量的临床前和临床研究强调了 miRs 在高血压肾病、糖尿病肾病、肾小球肾炎、肾间质纤维化以及一些相关心血管并发症发病机制中的潜在作用。在这篇综述中,我们将概述在 CKD 中研究的 miRs,特别是强调 miR-103a-3p、miR-192-5p、miR-29 家族和 miR-21-5p,因为它们最有可能产生新的治疗和诊断策略。