慢性肾病患者使用 SGLT2 抑制剂:支持心血管、肾脏和代谢健康

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Magdalena Madero , Glenn M. Chertow , Patrick B. Mark
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引用次数: 0

摘要

钠-葡萄糖共转运体-2(SGLT2)抑制剂最初是为治疗 2 型糖尿病(T2DM)而开发的,在大型结果试验中显示出多种心血管和肾脏保护作用。随后,它们被批准作为慢性肾脏病(CKD)的治疗药物,标志着慢性肾脏病治疗领域发生了关键性的转变。此外,dapagliflozin 和 empagliflozin 被批准用于伴有或不伴有 T2DM 的 CKD 患者,为这一人群提供了新的治疗机会。SGLT2 抑制剂是治疗慢性肾功能衰竭的有效药物,具有良好的安全性。然而,也许是由于医护人员缺乏确定性和熟悉度,SGLT2 抑制剂的使用一直很缓慢,尤其是在没有 T2DM 的患者中。随着慢性肾脏病管理的不断发展,医护人员应了解这些变化,并及时执行新的指南建议,以避免治疗惰性。SGLT2抑制剂被推荐用于伴有或不伴有T2DM的CKD患者,是支持心血管、肾脏和代谢健康的基础药物。在本综述中,我们对临床上可能提出的有关使用 SGLT2 抑制剂治疗 CKD 的问题进行了循证解答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SGLT2 Inhibitor Use in Chronic Kidney Disease: Supporting Cardiovascular, Kidney, and Metabolic Health

Originally developed for use in type 2 diabetes mellitus (T2DM), sodium–glucose co-transporter-2 (SGLT2) inhibitors demonstrated diverse cardiovascular- and kidney-protective effects in large outcome trials. Their subsequent approval as a treatment for chronic kidney disease (CKD) marked a pivotal shift in the landscape of CKD management. Further to this, the approval of dapagliflozin and empagliflozin for use in patients with CKD with and without T2DM afforded new treatment opportunities for this population. SGLT2 inhibitors provide an effective treatment for CKD with a favorable safety profile. However, their uptake has been slow, especially among patients without T2DM, owing perhaps to a lack of certainty and familiarity among health care professionals. As the landscape of CKD management continues to evolve, health care professionals should remain knowledgeable about these changes, and implement new guideline recommendations promptly to avoid therapeutic inertia. SGLT2 inhibitors are recommended for patients with CKD with or without T2DM and are foundational agents to support cardiovascular, kidney, and metabolic health. In this review, we provide evidence-based answers to questions that may be asked in the clinic regarding the use of SGLT2 inhibitors to treat CKD.

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来源期刊
Kidney Medicine
Kidney Medicine Medicine-Internal Medicine
CiteScore
4.80
自引率
5.10%
发文量
176
审稿时长
12 weeks
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