Department of Diabetology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.
Diabetes Unit, Department of Endocrinology and Metabolism, Hadassah Medical Centre, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Diabetes Obes Metab. 2024 Oct;26(10):4165-4177. doi: 10.1111/dom.15789. Epub 2024 Aug 14.
Chronic kidney disease (CKD) affects approximately 13% of people globally, including 20%-48% with type 2 diabetes (T2D), resulting in significant morbidity, mortality, and healthcare costs. There is an urgent need to increase early screening and intervention for CKD. We are experts in diabetology and nephrology in Central Europe and Israel. Herein, we review evidence supporting the use of sodium-glucose cotransporter-2 (SGLT2) inhibitors for kidney protection and discuss barriers to early CKD diagnosis and treatment, including in our respective countries. SGLT2 inhibitors exert cardiorenal protective effects, demonstrated in the renal outcomes trials (EMPA-KIDNEY, DAPA-CKD, CREDENCE) of empagliflozin, dapagliflozin, and canagliflozin in patients with CKD. EMPA-KIDNEY demonstrated cardiorenal efficacy across the broadest renal range, regardless of T2D status. Renoprotective evidence also comes from large real-world studies. International guidelines recommend first-line SGLT2 inhibitors for patients with T2D and estimated glomerular filtration rate (eGFR) ≥20 mL/min/1.73 m, and that glucagon-like peptide-1 receptor agonists may also be administered if required for additional glucose control. Although these guidelines recommend at least annual eGFR and urine albumin-to-creatinine ratio screening for patients with T2D, observational studies suggest that only half are screened. Diagnosis is hampered by asymptomatic early CKD and under-recognition among patients with T2D and clinicians, including limited knowledge/use of guidelines and resources. Based on our experience and on the literature, we recommend robust screening programmes, potentially with albuminuria self-testing, and SGLT2 inhibitor reimbursement at general practitioner (GP) and specialist levels. High-tech tools (artificial intelligence, smartphone apps, etc.) are providing exciting opportunities to identify high-risk individuals, self-screen, detect abnormalities in images, and assist with prescribing and treatment adherence. Better education is also needed, alongside provision of concise guidelines, enabling GPs to identify who would benefit from early initiation of renoprotective therapy; although, regardless of current renal function, cardiorenal protection is provided by SGLT2 inhibitor therapy.
慢性肾脏病(CKD)影响着全球约 13%的人群,其中 20%-48%为 2 型糖尿病(T2D)患者,由此导致了大量的发病率、死亡率和医疗保健费用。迫切需要增加 CKD 的早期筛查和干预。我们是中欧和以色列的糖尿病学和肾脏病学专家。在此,我们回顾了支持使用钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂进行肾脏保护的证据,并讨论了早期 CKD 诊断和治疗的障碍,包括在我们各自的国家。SGLT2 抑制剂在 CKD 患者的肾脏结局试验(EMPA-KIDNEY、DAPA-CKD、CREDENCE)中表现出心脏肾脏保护作用,证明了恩格列净、达格列净和卡格列净的疗效。EMPA-KIDNEY 显示出在最广泛的肾脏范围内的心脏肾脏疗效,无论 T2D 状态如何。来自大型真实世界研究的也有肾脏保护证据。国际指南建议将 SGLT2 抑制剂作为 T2D 患者和估算肾小球滤过率(eGFR)≥20ml/min/1.73m 的一线治疗药物,如果需要额外的血糖控制,也可以使用胰高血糖素样肽-1 受体激动剂。尽管这些指南建议 T2D 患者至少每年进行一次 eGFR 和尿白蛋白与肌酐比值筛查,但观察性研究表明,只有一半的患者接受了筛查。由于早期 CKD 无症状以及 T2D 患者和临床医生对其认识不足,包括对指南和资源的了解/使用有限,导致诊断受到阻碍。根据我们的经验和文献,我们建议建立强有力的筛查计划,可能包括白蛋白尿自我检测,以及在全科医生(GP)和专家层面报销 SGLT2 抑制剂。高科技工具(人工智能、智能手机应用程序等)为识别高风险个体、自我筛查、检测图像异常以及协助处方和治疗依从性提供了令人兴奋的机会。还需要更好的教育,同时提供简洁的指南,使全科医生能够确定谁将受益于早期开始肾脏保护治疗;尽管如此,无论当前的肾功能如何,SGLT2 抑制剂治疗都能提供心脏肾脏保护。