2 型糖尿病中的 GLP-1 受体激动剂和 SGLT2 抑制剂:多重心脏代谢效应和联合疗法的附加价值。

IF 13 1区 医学 Q1 PHARMACOLOGY & PHARMACY Drugs Pub Date : 2024-09-28 DOI:10.1007/s40265-024-02090-9
André J Scheen
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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)和钠-葡萄糖共转运体 2 抑制剂(SGLT2is)在随机临床试验和实际观察研究中证明了其有效性和安全性。除了改善血糖控制、减轻体重和降低动脉血压(替代终点)外,这些药物的突破性进展还包括显著减少了高危 2 型糖尿病患者的心血管和肾脏事件。GLP-1RAs 可减少与致动脉粥样硬化性心血管疾病(尤其是缺血性中风)相关的事件,也可减少肾脏疾病(使用 semaglutide 的 FLOW 试验),但对心力衰竭的影响有限。SGLT2is 最显著的保护作用是明显降低了心力衰竭的住院率,并显著降低了慢性肾病的进展。除降糖作用外,这些益处还归因于多种多效应。GLP-1RA(主要是抗动脉粥样硬化和血管效应)和 SGLT2is(主要是全身和肾内血流动力学变化)对心血管和肾脏保护的基本机制至少部分不同。因此,高危患者在接受 GLP-1RA/SGLT2i 联合用药治疗时,可能会从互补作用中获益。这种联合用药在替代终点上证明了其疗效。此外,心血管结果试验的事后亚组分析表明,与单一疗法相比,联合疗法对患者的心血管保护作用更大。一些回顾性队列研究也证实了联合疗法的益处。目前正在进行一项专门的前瞻性试验(PRECIDENTD),比较联合疗法与任一单一疗法的优劣;然而,仍然存在一些挑战,尤其是联合疗法的成本较高,而且全球范围内 GLP-1RAs 或 SGLT2is 在临床实践中使用不足,即使在心肾风险较高的患者中也是如此。
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GLP-1 Receptor Agonists and SGLT2 Inhibitors in Type 2 Diabetes: Pleiotropic Cardiometabolic Effects and Add-on Value of a Combined Therapy.

Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter 2 inhibitors (SGLT2is) have proven efficacy and safety in randomized clinical trials and observational real-life studies. Besides improving glucose control, reducing body weight, and lowering arterial blood pressure (surrogate endpoints), the breakthroughs were the demonstration of a significant reduction in cardiovascular and renal events in patients with type 2 diabetes at high risk. GLP-1RAs reduce events linked to atherogenic cardiovascular disease (especially ischemic stroke) and also renal outcomes (FLOW trial with semaglutide), with a limited effect on heart failure. The most striking protective effects of SGLT2is were a marked reduction in hospitalization for heart failure and a remarkable reduced progression of chronic kidney disease. These benefits have been attributed to numerous pleiotropic effects beyond glucose-lowering action. Underlying mechanisms contributing to cardiovascular and renal protection are at least partially different between GLP-1RAs (mainly anti-atherogenic and vascular effects) and SGLT2is (mainly systemic and intrarenal hemodynamic changes). Thus, patients at high risk may benefit from complementary actions when being treated with a GLP-1RA/SGLT2i combination. Such combination has proven its efficacy on surrogate endpoints. Furthermore, post hoc subgroup analyses of cardiovascular outcome trials have suggested a greater cardiorenal protection in patients treated with a combination versus either monotherapy. The benefits of a combined therapy have been confirmed in a few retrospective cohort studies. A dedicated prospective trial comparing a combined therapy versus either monotherapy is ongoing (PRECIDENTD); however, several challenges still remain, especially the higher cost of a combined therapy and the worldwide underuse of either GLP-1RAs or SGLT2is in clinical practice, even in patients at high cardiorenal risk.

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来源期刊
Drugs
Drugs 医学-毒理学
CiteScore
22.70
自引率
0.90%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Drugs is a journal that aims to enhance pharmacotherapy by publishing review and original research articles on key aspects of clinical pharmacology and therapeutics. The journal includes: Leading/current opinion articles providing an overview of contentious or emerging issues. Definitive reviews of drugs and drug classes, and their place in disease management. Therapy in Practice articles including recommendations for specific clinical situations. High-quality, well designed, original clinical research. Adis Drug Evaluations reviewing the properties and place in therapy of both newer and established drugs. AdisInsight Reports summarising development at first global approval. Moreover, the journal offers additional digital features such as animated abstracts, video abstracts, instructional videos, and podcasts to increase visibility and educational value. Plain language summaries accompany articles to assist readers with some knowledge of the field in understanding important medical advances.
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