Department of Nephrocardiology, Medical University of Lodz, Ul. Zeromskiego 113, 90-549 Lodz, Poland.
Department of Nephrology, Hypertension and Family Medicine, Medical University of Lodz, Ul. Zeromskiego 113, 90-549 Lodz, Poland.
Int J Mol Sci. 2024 Sep 23;25(18):10222. doi: 10.3390/ijms251810222.
Diabetic kidney disease (DKD) is a major complication of diabetes mellitus (DM), affecting over one-third of type 1 and nearly half of type 2 diabetes patients. As the leading cause of end-stage renal disease (ESRD) globally, DKD develops through a complex interplay of chronic hyperglycemia, oxidative stress, and inflammation. Early detection is crucial, with diagnosis based on persistent albuminuria and reduced estimated glomerular filtration rate (eGFR). Treatment strategies emphasize comprehensive management, including glycemic control, blood pressure regulation, and the use of nephroprotective agents such as angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), sodium-glucose cotransporter-2 (SGLT2) inhibitors, and glucagon-like peptide-1 (GLP-1) receptor agonists. Ongoing research explores novel therapies targeting molecular pathways and non-coding RNAs. Preventive measures focus on rigorous control of hyperglycemia and hypertension, aiming to mitigate disease progression. Despite therapeutic advances, DKD remains a leading cause of ESRD, highlighting the need for continued research to identify new biomarkers and innovative treatments.
糖尿病肾病(DKD)是糖尿病(DM)的一种主要并发症,影响超过三分之一的 1 型糖尿病患者和近一半的 2 型糖尿病患者。作为全球范围内导致终末期肾病(ESRD)的主要原因,DKD 通过慢性高血糖、氧化应激和炎症的复杂相互作用发展而来。早期检测至关重要,其诊断基于持续的白蛋白尿和估算肾小球滤过率(eGFR)降低。治疗策略强调综合管理,包括血糖控制、血压调节以及使用肾保护剂,如血管紧张素转换酶(ACE)抑制剂、血管紧张素 II 受体阻滞剂(ARBs)、钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂和胰高血糖素样肽-1(GLP-1)受体激动剂。目前正在研究针对分子途径和非编码 RNA 的新型疗法。预防措施侧重于严格控制高血糖和高血压,以减缓疾病进展。尽管治疗取得了进展,但 DKD 仍然是 ESRD 的主要原因,这突出表明需要继续研究以确定新的生物标志物和创新的治疗方法。
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