GLP-1受体激动剂以及与SGLT2抑制剂和非格列酮联合疗法对心血管和肾脏影响的最新证据:叙述性综述和展望。

IF 8.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Kosuke Sawami, Atsushi Tanaka, Koichi Node
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引用次数: 0

摘要

胰高血糖素样肽-1 受体激动剂(GLP-1RA)具有可靠的降血糖和减肥效果,可以干预肥胖,而肥胖是 2 型糖尿病的病理基础。GLP-1RA 疗法在降低主要不良心血管事件风险和改善心血管疾病高风险糖尿病患者的肾脏预后方面具有潜在的益处。最近有证据表明,GLP-1RA 还可用于治疗射血分数保留型心力衰竭,并改善糖尿病患者和非糖尿病患者的肾脏临床疗效。一些大型临床试验的子分析表明,GLP-1RA 和钠-葡萄糖共转运体 2 抑制剂联合治疗可比单独治疗更显著地减少心衰住院和肾脏复合事件。此外,在这种联合疗法中加入非格列酮可能会带来更强的心肾保护作用。还需要进一步的研究来评估联合疗法对心血管和肾脏的潜在益处,并确定适合接受该疗法的患者人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Updated evidence on cardiovascular and renal effects of GLP-1 receptor agonists and combination therapy with SGLT2 inhibitors and finerenone: a narrative review and perspectives.

Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have a reliable hypoglycaemic and weight-loss effect that can intervene in obesity, which is the basis of type 2 diabetes pathology. GLP-1RA therapy has shown potential benefits in reducing the risk of major adverse cardiovascular events and improving kidney outcomes in patients with diabetes at high risk for cardiovascular disease. More recent evidence is expanding their benefits to heart failure with preserved ejection fraction and clinically important renal outcomes in patients with and without diabetes. Some sub-analyses of large clinical trials suggest that GLP-1RA and sodium-glucose cotransporter 2 inhibitor combination therapy may provide more significant reductions in heart failure hospitalization and renal composite events than each alone. Moreover, the addition of finerenone to this combination therapy could potentially provide stronger cardiorenal protective benefits. Further studies are needed to assess the potential cardiovascular and renal benefits of combination therapy and to determine suitable patient population for the therapy.

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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
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