Department of Diabetology, CHU de Rennes, Université de Rennes 1, Rennes, France.
Department of Diabetes, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Diabetes Obes Metab. 2024 Nov;26 Suppl 6:55-65. doi: 10.1111/dom.15710. Epub 2024 Jun 20.
Diabetic nephropathy, also known as diabetic kidney disease (DKD), remains a challenge in clinical practice as this is the major cause of kidney failure worldwide. Clinical trials do not answer all the questions raised in clinical practice and real-world evidence provides complementary insights from randomized controlled trials. Real-life longitudinal data highlight the need for improved screening and management of diabetic nephropathy in primary care. Adherence to the recommended guidelines for comprehensive care appears to be suboptimal in clinical practice in patients with DKD. Barriers to the initiation of sodium-glucose cotransporter-2 (SGLT2) inhibitors for patients with DKD persist in clinical practice, in particular for the elderly. Attainment of blood pressure targets often remains an issue. Initiation of glucagon-like peptide-1 receptor agonists (GLP-1RAs) in routine clinical practice is associated with a reduced risk of albuminuria progression and a possible beneficial effect on kidney function. Real-world evidence confirms a beneficial effect of SGLT2 inhibitors on the decline of glomerular filtration, even in the absence of albuminuria, with a lower risk of acute kidney injury events compared to GLP-1RA use. In addition, SGLT2 inhibitors confer a lower risk of hyperkalaemia after initiation compared with dipeptidyl peptidase-4 inhibitors in patients with DKD. Data from a large population indicate that diuretic treatment increases the risk of a significant decline in glomerular filtration rate in the first few weeks of treatment after SGLT2 inhibitor initiation. The perspective for a global approach targeting multifaceted criteria for diabetic individuals with DKD is emerging based on real-world evidence but there is still a long way to go to achieve this goal.
糖尿病肾病,又称糖尿病肾脏疾病(DKD),仍然是临床实践中的一个挑战,因为这是全球范围内导致肾衰竭的主要原因。临床试验并不能回答临床实践中提出的所有问题,而真实世界证据则提供了来自随机对照试验的补充见解。真实世界的纵向数据突出表明,需要在初级保健中改进对糖尿病肾病的筛查和管理。在 DKD 患者的临床实践中,对推荐的综合护理指南的依从性似乎并不理想。在临床实践中,对于 DKD 患者,启动钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂的障碍仍然存在,特别是对于老年人而言。血压目标的实现往往仍然是一个问题。在常规临床实践中启动胰高血糖素样肽-1 受体激动剂(GLP-1RAs)与蛋白尿进展风险降低以及对肾功能的可能有益影响相关。真实世界的证据证实,SGLT2 抑制剂可降低肾小球滤过率的下降,即使在没有蛋白尿的情况下也是如此,与 GLP-1RA 相比,急性肾损伤事件的风险较低。此外,与 DKD 患者的二肽基肽酶-4 抑制剂相比,SGLT2 抑制剂在启动后发生高钾血症的风险较低。来自大型人群的数据表明,在 SGLT2 抑制剂启动后最初几周的治疗中,利尿剂治疗会增加肾小球滤过率显著下降的风险。基于真实世界的证据,针对具有 DKD 的糖尿病个体的多方面标准的全球方法的观点正在出现,但要实现这一目标还有很长的路要走。