Caruso Irene, Cignarelli Angelo, Sorice Gian Pio, Natalicchio Annalisa, Perrini Sebastio, Laviola Luigi, Giorgino Francesco
Department of Emergency and Organ Transplantation Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, 70124 Bari, Italy.
Metabolites. 2022 Feb 15;12(2):183. doi: 10.3390/metabo12020183.
Cardiovascular outcome trials (CVOT) showed that treatment with glucagon-like peptide-1 receptor agonists (GLP-1RA) is associated with significant cardiovascular benefits. However, CVOT are scarcely representative of everyday clinical practice, and real-world studies could provide clinicians with more relatable evidence. Here, literature was thoroughly searched to retrieve real-world studies investigating the cardiovascular and renal outcomes of GLP-1RA vs. other glucose-lowering drugs and carry out relevant meta-analyses thereof. Most real-world studies were conducted in populations at low cardiovascular and renal risk. Of note, real-world studies investigating cardio-renal outcomes of GLP-1RA suggested that initiation of GLP-1RA was associated with a greater benefit on composite cardiovascular outcomes, MACE (major adverse cardiovascular events), all-cause mortality, myocardial infarction, stroke, cardiovascular death, peripheral artery disease, and heart failure compared to other glucose-lowering drugs with the exception of sodium-glucose transporter-2 inhibitors (SGLT-2i). Initiation of SGLT-2i and GLP-1RA yielded similar effects on composite cardiovascular outcomes, MACE, stroke, and myocardial infarction. Conversely, GLP-1RA were less effective on heart failure prevention compared to SGLT-2i. Finally, the few real-world studies addressing renal outcomes suggested a significant benefit of GLP-1RA on estimated glomerular filtration rate (eGFR) reduction and hard renal outcomes vs. active comparators except SGLT-2i. Further real-world evidence is needed to clarify the role of GLP-1RA in cardio-renal protection among available glucose-lowering drugs.
心血管结局试验(CVOT)表明,使用胰高血糖素样肽-1受体激动剂(GLP-1RA)进行治疗具有显著的心血管益处。然而,CVOT几乎不能代表日常临床实践,而真实世界研究可以为临床医生提供更具相关性的证据。在此,我们全面检索了文献,以获取调查GLP-1RA与其他降糖药物相比的心血管和肾脏结局的真实世界研究,并对其进行相关的荟萃分析。大多数真实世界研究是在心血管和肾脏风险较低的人群中进行的。值得注意的是,调查GLP-1RA心脏和肾脏结局的真实世界研究表明,与除钠-葡萄糖协同转运蛋白-2抑制剂(SGLT-2i)之外的其他降糖药物相比,起始使用GLP-1RA与复合心血管结局、主要不良心血管事件(MACE)、全因死亡率、心肌梗死、中风、心血管死亡、外周动脉疾病和心力衰竭方面的更大益处相关。起始使用SGLT-2i和GLP-1RA在复合心血管结局、MACE、中风和心肌梗死方面产生相似的效果。相反,与SGLT-2i相比,GLP-1RA在预防心力衰竭方面效果较差。最后,少数涉及肾脏结局的真实世界研究表明,与除SGLT-2i之外的活性对照药物相比,GLP-1RA在估计肾小球滤过率(eGFR)降低和严重肾脏结局方面具有显著益处。需要更多真实世界证据来阐明GLP-1RA在现有降糖药物的心脏和肾脏保护中的作用。