Emerging Preventive Strategies in Chronic Kidney Disease: Recent Evidence and Gaps in Knowledge.

IF 5.7 2区 医学 Q1 PERIPHERAL VASCULAR DISEASE
Nishigandha Pradhan, Mirela Dobre
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Abstract

Purpose of review: Chronic kidney disease (CKD) is increasingly prevalent worldwide and is associated with increased cardiovascular risk. New therapeutic options to slow CKD progression and reduce cardiovascular morbidity and mortality have recently emerged. This review highlights recent evidence and gaps in knowledge in emerging CKD preventive strategies.

Recent findings: EMPA-Kidney trial found that empagliflozin, a sodium-glucose co-transporter 2 inhibitor (SGLT2i) led to 28% lower risk of progression of kidney disease or death from cardiovascular causes, compared to placebo. This reinforced the previous findings from DAPA-CKD and CREDENCE trials and led to inclusion of SGLT2i as the cornerstone of CKD preventive therapy in both diabetic and non-diabetic CKD. Finerenone, a selective nonsteroidal mineralocorticoid receptor antagonist, slowed diabetic kidney disease progression by 23% compared to placebo in a pool analysis of FIDELIO-DKD and FIGARO-DKD trials. Non-pharmacological interventions, including low protein diet, and early CKD detection and risk stratification strategies based on novel biomarkers have also gained momentum. Ongoing efforts to explore the wealth of molecular mechanisms in CKD, added to integrative omics modeling are well posed to lead to novel therapeutic targets in kidney care. While breakthrough pharmacological interventions continue to improve outcomes in CKD, the heterogeneity of kidney diseases warrants additional investigation. Further research into specific kidney disease mechanisms will facilitate the identification of patient populations most likely to benefit from targeted interventions.

Abstract Image

慢性肾脏疾病的新兴预防策略:最新证据和知识空白。
综述目的:慢性肾脏疾病(CKD)在世界范围内越来越普遍,并与心血管风险增加有关。最近出现了减缓CKD进展和降低心血管发病率和死亡率的新治疗选择。这篇综述强调了新近出现的CKD预防策略的证据和知识差距。最近的发现:EMPA-Kidney试验发现,与安慰剂相比,钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)恩格列净导致肾脏疾病进展或心血管原因死亡的风险降低28%。这加强了先前DAPA-CKD和CREDENCE试验的发现,并导致将SGLT2i纳入糖尿病和非糖尿病性CKD预防治疗的基础。在FIDELIO-DKD和FIGARO-DKD试验的池分析中,选择性非甾体类矿物皮质激素受体拮抗剂菲纳酮比安慰剂延缓糖尿病肾病进展23%。非药物干预,包括低蛋白饮食、早期CKD检测和基于新型生物标志物的风险分层策略也获得了发展势头。正在进行的探索CKD丰富的分子机制的努力,加上整合组学建模,很好地引导了肾脏护理的新治疗靶点。虽然突破性的药物干预继续改善CKD的预后,但肾脏疾病的异质性值得进一步研究。对特定肾脏疾病机制的进一步研究将有助于确定最有可能从针对性干预中受益的患者群体。
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来源期刊
CiteScore
9.00
自引率
3.40%
发文量
87
审稿时长
6-12 weeks
期刊介绍: The aim of this journal is to systematically provide expert views on current basic science and clinical advances in the field of atherosclerosis and highlight the most important developments likely to transform the field of cardiovascular prevention, diagnosis, and treatment. We accomplish this aim by appointing major authorities to serve as Section Editors who select leading experts from around the world to provide definitive reviews on key topics and papers published in the past year. We also provide supplementary reviews and commentaries from well-known figures in the field. An Editorial Board of internationally diverse members suggests topics of special interest to their country/region and ensures that topics are current and include emerging research.
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