Epelde Francisco
Medicine Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí I3PT, 08208 Sabadell, Spain.
Medicina (Kaunas). 2024 Dec 2;60(12):1986. doi: 10.3390/medicina60121986.
The increasing prevalence of both type 2 diabetes mellitus and heart failure has underscored the urgent need for optimized therapeutic strategies that address the complex interplay between these conditions. Dipeptidyl peptidase-4 (DPP-4) inhibitors have emerged as a popular class of glucose-lowering agents due to their favorable glycemic effects, safety profile, and potential cardiovascular benefits. However, the impact of DPP-4 inhibitors on heart failure outcomes in patients with diabetes remains contentious, with conflicting evidence from clinical trials and observational studies. This review critically examines current evidence on the use of DPP-4 inhibitors in patients with coexisting diabetes and heart failure, focusing on pharmacodynamics, safety, and efficacy outcomes. We explore the physiological mechanisms by which DPP-4 inhibitors may influence heart failure risk, including modulation of inflammation, oxidative stress, and myocardial fibrosis. Clinical trials such as SAVOR-TIMI 53, EXAMINE, and TECOS are evaluated to provide a comprehensive analysis of DPP-4 inhibitors' effects on hospitalization for heart failure, mortality, and cardiovascular events in diabetic patients. While some trials suggest an increased risk of HF hospitalizations with specific DPP-4 inhibitors (e.g., saxagliptin), others report neutral effects, raising questions about the class effects versus individual drug characteristics within this group. Additionally, we address discrepancies in outcomes related to patient demographics, HF phenotype, and comorbid conditions that may influence DPP-4 inhibitors' risk-benefit profile. Comparative insights into alternative glucose-lowering therapies such as SGLT2 inhibitors and GLP-1 receptor agonists are also provided, highlighting potential implications for treatment selection in this high-risk population. In summary, this review synthesizes available evidence on DPP-4 inhibitors' impact in diabetic patients with heart failure, aiming to guide clinicians in making informed therapeutic decisions. While DPP-4 inhibitors remain a viable option in diabetes management, caution is warranted in patients with advanced heart failure, and future research is essential to refine patient-specific guidelines.
2型糖尿病和心力衰竭的患病率不断上升,凸显了迫切需要优化治疗策略,以应对这两种疾病之间复杂的相互作用。二肽基肽酶-4(DPP-4)抑制剂因其良好的血糖控制效果、安全性以及潜在的心血管益处,已成为一类广受欢迎的降糖药物。然而,DPP-4抑制剂对糖尿病患者心力衰竭结局的影响仍存在争议,临床试验和观察性研究的证据相互矛盾。本综述批判性地审视了目前关于DPP-4抑制剂在合并糖尿病和心力衰竭患者中应用的证据,重点关注药效学、安全性和疗效结局。我们探讨了DPP-4抑制剂可能影响心力衰竭风险的生理机制,包括炎症调节、氧化应激和心肌纤维化。对SAVOR-TIMI 53、EXAMINE和TECOS等临床试验进行了评估,以全面分析DPP-4抑制剂对糖尿病患者因心力衰竭住院、死亡率和心血管事件的影响。虽然一些试验表明特定的DPP-4抑制剂(如沙格列汀)会增加心力衰竭住院风险,但其他试验报告结果呈中性,这引发了关于该类药物的总体效应与组内个别药物特性的疑问。此外,我们还探讨了与患者人口统计学、心力衰竭表型和合并症相关的结局差异,这些因素可能会影响DPP-4抑制剂的风险效益概况。还提供了对其他降糖疗法(如钠-葡萄糖协同转运蛋白2抑制剂和胰高血糖素样肽-1受体激动剂)的比较见解,强调了对这一高危人群治疗选择的潜在影响。总之,本综述综合了关于DPP-4抑制剂对心力衰竭糖尿病患者影响的现有证据,旨在指导临床医生做出明智的治疗决策。虽然DPP-4抑制剂在糖尿病管理中仍然是一个可行的选择,但对于晚期心力衰竭患者需要谨慎使用,未来的研究对于完善针对特定患者的指南至关重要。