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改善糖尿病肾病临床结局的新策略。

New strategies to improve clinical outcomes for diabetic kidney disease.

机构信息

Clinical Research Services, Mannheim GmbH, Grenadierstrasse 1, D-68167, Mannheim, Germany.

Department of Endocrinology, UZ Gasthuisberg, Katholieke Universiteit, Leuven, Belgium.

出版信息

BMC Med. 2022 Oct 10;20(1):337. doi: 10.1186/s12916-022-02539-2.

DOI:10.1186/s12916-022-02539-2
PMID:36210442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9548386/
Abstract

BACKGROUND

Diabetic kidney disease (DKD), the most common cause of kidney failure and end-stage kidney disease worldwide, will develop in almost half of all people with type 2 diabetes. With the incidence of type 2 diabetes continuing to increase, early detection and management of DKD is of great clinical importance.

MAIN BODY

This review provides a comprehensive clinical update for DKD in people with type 2 diabetes, with a special focus on new treatment modalities. The traditional strategies for prevention and treatment of DKD, i.e., glycemic control and blood pressure management, have only modest effects on minimizing glomerular filtration rate decline or progression to end-stage kidney disease. While cardiovascular outcome trials of SGLT-2i show a positive effect of SGLT-2i on several kidney disease-related endpoints, the effect of GLP-1 RA on kidney-disease endpoints other than reduced albuminuria remain to be established. Non-steroidal mineralocorticoid receptor antagonists also evoke cardiovascular and kidney protective effects.

CONCLUSION

With these new agents and the promise of additional agents under clinical development, clinicians will be more able to personalize treatment of DKD in patients with type 2 diabetes.

摘要

背景

糖尿病肾病(DKD)是全球范围内导致肾衰竭和终末期肾病的最常见病因,几乎所有 2 型糖尿病患者中都会发生。随着 2 型糖尿病的发病率持续上升,早期发现和管理 DKD 具有重要的临床意义。

主体

本文对 2 型糖尿病患者的 DKD 进行了全面的临床更新,特别关注新的治疗方法。预防和治疗 DKD 的传统策略,即血糖控制和血压管理,对减缓肾小球滤过率下降或进展为终末期肾病的效果有限。SGLT-2i 的心血管结局试验表明 SGLT-2i 对几个与肾脏疾病相关的终点有积极影响,但 GLP-1RA 对除减少白蛋白尿以外的肾脏疾病终点的影响仍有待确定。非甾体类盐皮质激素受体拮抗剂也具有心血管和肾脏保护作用。

结论

随着这些新药物的出现,以及更多正在临床开发中的药物的出现,临床医生将能够更好地为 2 型糖尿病患者的 DKD 进行个体化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/7aa562dc28d9/12916_2022_2539_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/7d3426d6a5b0/12916_2022_2539_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/c2f4a1de8d1c/12916_2022_2539_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/7aa562dc28d9/12916_2022_2539_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/7d3426d6a5b0/12916_2022_2539_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/89d73f6a30f9/12916_2022_2539_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/c2f4a1de8d1c/12916_2022_2539_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74e2/9549617/7aa562dc28d9/12916_2022_2539_Fig4_HTML.jpg

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2
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Eur Heart J. 2022 Feb 10;43(6):474-484. doi: 10.1093/eurheartj/ehab777.
3
Update on pathogenesis and diagnosis flow of normoalbuminuric diabetes with renal insufficiency.
Global, regional, and national burden of chronic kidney disease among adolescents and emerging adults from 1990 to 2021.1990年至2021年全球、区域和国家青少年及青年慢性肾脏病负担
Ren Fail. 2025 Dec;47(1):2508296. doi: 10.1080/0886022X.2025.2508296. Epub 2025 May 22.
4
Relationship between weekend catch-up sleep and the risk of diabetic kidney disease.周末补觉与糖尿病肾病风险之间的关系。
Arch Endocrinol Metab. 2025 May 5;69(2):e240370. doi: 10.20945/2359-4292-2024-0370.
5
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Acta Diabetol. 2025 Apr 1. doi: 10.1007/s00592-025-02492-5.
6
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Front Endocrinol (Lausanne). 2025 Feb 21;16:1513008. doi: 10.3389/fendo.2025.1513008. eCollection 2025.
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Int J Stem Cells. 2025 May 30;18(2):158-172. doi: 10.15283/ijsc24113. Epub 2025 Jan 6.
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Am J Transl Res. 2024 Nov 15;16(11):6852-6866. doi: 10.62347/MCEE4840. eCollection 2024.
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