Department of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Int J Mol Sci. 2024 Sep 19;25(18):10051. doi: 10.3390/ijms251810051.
Diabetic kidney disease (DKD) is a common microvascular complication of diabetes mellitus (DM). With the increasing prevalence of DM worldwide, the incidence of DKD remains high. If DKD is not well controlled, it can develop into chronic kidney disease or end-stage renal disease (ESRD), which places considerable economic pressure on society. Traditional therapies, including glycemic control, blood pressure control, blood lipid control, the use of renin-angiotensin system blockers and novel drugs, such as sodium-glucose cotransporter 2 inhibitors, mineralocorticoid receptor inhibitors and glucagon-like peptide-1 receptor agonists, have been used in DKD patients. Although the above treatment strategies can delay the progression of DKD, most DKD patients still ultimately progress to ESRD. Therefore, new and multimodal treatment methods need to be explored. In recent years, researchers have continuously developed new treatment methods and targets to delay the progression of DKD, including miRNA therapy, stem cell therapy, gene therapy, gut microbiota-targeted therapy and lifestyle intervention. These new molecular therapy methods constitute opportunities to better understand and treat DKD. In this review, we summarize the progress of molecular therapeutics for DKD, leading to new treatment strategies.
糖尿病肾病(DKD)是糖尿病(DM)的一种常见微血管并发症。随着全球 DM 的患病率不断增加,DKD 的发病率仍然居高不下。如果 DKD 得不到很好的控制,它可能会发展为慢性肾病或终末期肾病(ESRD),这会给社会带来相当大的经济压力。传统的治疗方法,包括血糖控制、血压控制、血脂控制、肾素-血管紧张素系统阻滞剂和新型药物的使用,如钠-葡萄糖共转运蛋白 2 抑制剂、盐皮质激素受体抑制剂和胰高血糖素样肽-1 受体激动剂,已经被用于 DKD 患者。尽管上述治疗策略可以延缓 DKD 的进展,但大多数 DKD 患者最终仍会进展为 ESRD。因此,需要探索新的、多模式的治疗方法。近年来,研究人员不断开发新的治疗方法和靶点来延缓 DKD 的进展,包括 miRNA 治疗、干细胞治疗、基因治疗、肠道微生物群靶向治疗和生活方式干预。这些新的分子治疗方法为更好地理解和治疗 DKD 提供了机会。在这篇综述中,我们总结了 DKD 的分子治疗进展,从而为新的治疗策略提供了依据。