Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan.
Tokyo New Drug Research Laboratories, Kowa Company, Ltd., Tokyo, Japan.
Sci Rep. 2022 Mar 24;12(1):5129. doi: 10.1038/s41598-022-09059-2.
Dipeptidyl-peptidase-4 inhibitors (DPP4i) have been the most used antidiabetic medications worldwide due to their good safety profiles and tolerability with a low risk of hypoglycemia, however, large cardiovascular outcome trials (CVOTs) have not shown any significant the prognostic superiority. On the contrary, since observational studies have suggested the effects of DPP4i are enhanced some populations, such as Asians and those who without overweight, their prognostic benefit is still under debate. The aim of this study was thus to assess the prognostic impact of DPP4i in patients with both diabetes and coronary artery disease (CAD) who underwent percutaneous coronary intervention (PCI) through the insulin-like growth factor-1 (IGF-1) axis, a substrate of DPP4. This single-center analysis involved consecutive Japanese diabetic patients who underwent PCI for the first time between 2008 and 2018 (n = 885). Primary and secondary endpoints were set as cardiovascular (CV) death and the composite of CV death, non-fatal myocardial infarction and ischemic stroke (3P-MACE). Serum levels of IGF-1 and its main binding protein (insulin-like growth factor binding protein-3: IGFBP-3) were measured. In consequences, unadjusted Kaplan-Meier analyses revealed reduced incidences of CV-death and 3P-MACE by DPP4i, which was particularly enhanced in patients who were not overweight (BMI ≤ 25). Multivariate Cox hazard analyses consistently indicated reduced risks of CV death by DPP4i at PCI (hazard ratio (HR) 0.39, 95% confidence interval (CI) 0.16-0.82, p = 0.01) and 3P-MACE (HR 0.47, 95% CI 0.25-0.84, p = 0.01), respectively. Moreover, elevated IGF-1 activity indicated by the IGF-1/IGFBP-3 ratio was associated with decreased risks of both endpoints and it was significantly higher in patients with DPP4i (p < 0.0001). In conclusion, the findings of the present study indicate beneficial effects of DPP4i to improve outcomes in Japanese diabetic patients following PCI, which might be mediated by DPP4-IGF-1 axis.
二肽基肽酶-4 抑制剂(DPP4i)因其良好的安全性和耐受性,低血糖风险低,已成为全球最常用的抗糖尿病药物,但大型心血管结局试验(CVOT)并未显示出任何显著的预后优势。相反,由于观察性研究表明 DPP4i 在某些人群中的作用增强,例如亚洲人和非超重人群,其预后获益仍存在争议。因此,本研究旨在通过二肽基肽酶-4 的底物胰岛素样生长因子-1(IGF-1)轴评估 DPP4i 在接受经皮冠状动脉介入治疗(PCI)的糖尿病合并冠状动脉疾病(CAD)患者中的预后影响。这项单中心分析纳入了 2008 年至 2018 年间首次接受 PCI 的连续日本糖尿病患者(n=885)。主要和次要终点分别设定为心血管(CV)死亡和 CV 死亡、非致死性心肌梗死和缺血性卒中的复合终点(3P-MACE)。测量了 IGF-1 及其主要结合蛋白(胰岛素样生长因子结合蛋白 3:IGFBP-3)的血清水平。结果,未经调整的 Kaplan-Meier 分析显示,DPP4i 降低了 CV 死亡和 3P-MACE 的发生率,在不超重(BMI≤25)的患者中这种作用更为明显。多变量 Cox 风险分析一致表明,DPP4i 在 PCI 时降低了 CV 死亡的风险(风险比(HR)0.39,95%置信区间(CI)0.16-0.82,p=0.01)和 3P-MACE(HR 0.47,95%CI 0.25-0.84,p=0.01)。此外,IGF-1/IGFBP-3 比值升高表明 IGF-1 活性升高,与两个终点的风险降低相关,并且在使用 DPP4i 的患者中明显更高(p<0.0001)。总之,本研究的结果表明,DPP4i 可改善日本糖尿病患者 PCI 后的结局,这可能是通过 DPP4-IGF-1 轴介导的。