Tsai Jun-Li, Chen Cheng-Hsu, Wu Ming-Ju, Tsai Shang-Feng
Division of Family Medicine, Cheng Ching General Hospital, Taichung 407, Taiwan.
Division of Family Medicine, Cheng Ching Rehabilitation Hospital, Taichung 407, Taiwan.
Biomedicines. 2022 Apr 9;10(4):876. doi: 10.3390/biomedicines10040876.
Diabetic nephropathy (DN) is the main cause of end-stage kidney disease (ESKD). DN-related ESKD has the worst prognosis for survival compared with other causes. Due to the complex mechanisms of DN and the heterogeneous presentations, unmet needs exist for the renal outcome of diabetes mellitus. Clinical evidence for treating DN is rather solid. For example, the first Kidney Disease: Improving Global Outcomes (KDIGO) guideline was published in October 2020: KDIGO Clinical Practice Guideline for Diabetes Management in Chronic Kidney Disease. In December of 2020, the International Society of Nephrology published 60 (+1) breakthrough discoveries in nephrology. Among these breakthroughs, four important ones after 1980 were recognized, including glomerular hyperfiltration theory, renal protection by renin-angiotensin system inhibition, hypoxia-inducible factor, and sodium-glucose cotransporter 2 inhibitors. Here, we present a review on the pivotal and new mechanisms of DN from the implications of clinical studies and medications.
糖尿病肾病(DN)是终末期肾病(ESKD)的主要病因。与其他病因导致的ESKD相比,DN相关的ESKD生存预后最差。由于DN的发病机制复杂且临床表现多样,糖尿病肾病的肾脏转归仍存在未满足的需求。治疗DN的临床证据相当确凿。例如,首个《改善全球肾脏病预后组织(KDIGO)临床实践指南:慢性肾脏病糖尿病管理》于2020年10月发布;2020年12月,国际肾脏病学会公布了60项(+1项)肾脏病领域的突破性发现。在这些突破中,确认了1980年之后的四项重要发现,包括肾小球高滤过理论、肾素-血管紧张素系统抑制的肾脏保护作用、缺氧诱导因子以及钠-葡萄糖协同转运蛋白2抑制剂。在此,我们从临床研究和药物应用的角度,对DN的关键新机制进行综述。