Villalvazo Priscila, Villavicencio Carlos, Gonzalez de Rivera Marina, Fernandez-Fernandez Beatriz, Ortiz Alberto
Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz UAM, Madrid, Spain.
RICORS2040, Madrid, Spain.
Nephron. 2025;149(1):29-35. doi: 10.1159/000540307. Epub 2024 Jul 29.
Diabetic kidney disease is the most common driver of chronic kidney disease (CKD)-associated mortality and kidney replacement therapy. Despite recent therapeutic advances (sodium glucose co-transporter 2 [SGLT2] inhibitors, finerenone), the residual kidney and mortality risk remains high for patients already diagnosed of having CKD (i.e., estimated glomerular filtration rate <60 mL/min/1.73 m2 or urinary albumin:creatinine ratio >30 mg/g). The challenge for the near future is to identify patients at higher risk of developing CKD to initiate therapy before CKD develops (primary prevention of CKD) and to identify patients with CKD and high risk of progression or death, in order to intensify therapy. We now discuss recent advances in biomarkers that may contribute to the identification of such high-risk individuals for clinical trials of novel primary prevention or treatment approaches for CKD. The most advanced biomarker from a clinical development point of view is the urinary peptidomics classifier CKD273, that integrates prognostic information from 273 urinary peptides and identifies high-risk individuals before CKD develops.
糖尿病肾病是慢性肾脏病(CKD)相关死亡率和肾脏替代治疗的最常见驱动因素。尽管近期有治疗进展(钠-葡萄糖协同转运蛋白2 [SGLT2] 抑制剂、非奈利酮),但对于已被诊断患有CKD的患者(即估计肾小球滤过率<60 mL/min/1.73 m²或尿白蛋白与肌酐比值>30 mg/g),残余肾脏和死亡风险仍然很高。近期的挑战是识别有更高CKD发生风险的患者,以便在CKD发生之前启动治疗(CKD的一级预防),并识别有CKD且进展或死亡风险高的患者,从而强化治疗。我们现在讨论生物标志物的最新进展,这些进展可能有助于识别此类高危个体,用于CKD新型一级预防或治疗方法的临床试验。从临床开发角度来看,最先进的生物标志物是尿液肽组学分类器CKD273,它整合了来自273种尿液肽的预后信息,并在CKD发生之前识别高危个体。