[Progression inhibition in chronic kidney disease].

IF 0.6
Innere Medizin (Heidelberg, Germany) Pub Date : 2026-08-01 Epub Date: 2026-07-03 DOI:10.1007/s00108-026-02145-x
Julia Weinmann-Menke, Jan Galle
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Abstract

The KDIGO guidelines 2024 on evaluation and treatment of chronic kidney disease (CKD) represent a comprehensive update of the 2012 guidelines, incorporating evidence from over 937 references across 197 pages. The guidelines retain the established CGA classification system (cause, glomerular filtration rate, GFR category, albuminuria category) while introducing strengthened recommendations for prevention of CKD progression. Key advances include expanded indications for sodium-glucose transporter 2 (SGLT2) inhibitors regardless of diabetes status (grade 1A recommendation for eGFR ≥ 20 ml/min per 1.73 m2 body surface area), integration of nonsteroidal mineralocorticoid receptor antagonists (ns-MRA) for diabetic CKD and recognition of glucagon-like peptide‑1 receptor agonists (GLP‑1 RA) for cardiovascular and kidney protection. The guidelines emphasize comprehensive risk stratification, lifestyle optimization including dietary protein restriction (0.8 g/kg and day) and sodium limitation (2 g/day), blood pressure targets (120 mm Hg systolic when tolerable) and combination pharmacotherapy. Emerging therapy approaches including endothelin receptor antagonists and aldosterone synthase inhibitors show promise in phase 2 trials. Meta-analyses demonstrate that combination therapy with SGLT2 inhibitors, GLP‑1 RA, and ns-MRA can extend cardiovascular and kidney event-free survival by 3-5 years in high-risk patients with type 2 diabetes.

[慢性肾病的进展抑制]。
2024年KDIGO慢性肾脏疾病(CKD)评估和治疗指南是对2012年指南的全面更新,纳入了来自197页937多篇参考文献的证据。指南保留了已建立的CGA分类系统(病因、肾小球滤过率、GFR类别、蛋白尿类别),同时引入了预防CKD进展的强化建议。关键进展包括扩大了钠-葡萄糖转运蛋白2 (SGLT2)抑制剂的适应症,无论糖尿病状态如何(eGFR≥ 20 ml/min / 1.73 m2体表面积推荐1A级),整合非甾体矿皮质激素受体拮抗剂(ns-MRA)治疗糖尿病性CKD,识别胰高血糖素样肽- 1受体激动剂(GLP - 1 RA)用于心血管和肾脏保护。该指南强调全面的风险分层、生活方式优化,包括饮食蛋白质限制(0.8 g/kg和天)和钠限制(2 g/天)、血压目标(可耐受时收缩压120 mm Hg)和联合药物治疗。新兴的治疗方法包括内皮素受体拮抗剂和醛固酮合成酶抑制剂在2期试验中显示出希望。荟萃分析表明,SGLT2抑制剂、GLP‑1 RA和ns-MRA联合治疗可将高危2型糖尿病患者的心血管和肾脏无事件生存期延长3-5年。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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