Mo Qiu, Adam Terrence J, Johnson Steven G, Moheet Amir, Pieczkiewicz David S
Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA.
College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Sci Rep. 2025 Jul 16;15(1):25735. doi: 10.1038/s41598-025-10299-1.
The comparative renoprotective effects of metformin-GLP-1 RA (glucagon-like peptide 1 receptor agonist), metformin-DPP-4i (dipeptidyl peptidase 4 inhibitor) and metformin-oADM (other antidiabetes medication) in patients with DKD (diabetic kidney disease) were evaluated by assessing the associations between renal impairment and combination therapies. Patients initially diagnosed with DKD between January 1, 2010, and January 1, 2017, were included. Those receiving combination treatment with metformin-GLP-1 RA, metformin-DPP-4i, or metformin-oADM were selected and paired. A logistic regression model was applied to generate odds ratios with 95% confidence intervals to assess the associations between the composite renal impairment outcomes and the combination ADM (antidiabetes medication) groups. Sensitivity analyses were also performed. Renal impairment was significantly reduced in patients who were treated with metformin-GLP-1 RA than in those treated with metformin-DPP-4i in the primary and secondary analyses (OR 0.60, P < 0.05 for the primary outcome; OR 0.44, P < 0.05 for the secondary outcome). The associations of renal impairment risk and ADM combination therapies with metformin-DPP-4i versus metformin-oADM were not statistically significant in either the primary or secondary analysis (OR = 1.22, P = 0.20 for the primary outcome; OR = 0.90, P = 0.53 for the secondary outcome). The results of the sensitivity analyses were consistent with those of the main analysis. The combination metformin-GLP-1 RA was associated with fewer renal impairment events compared to metformin-DPP-4i and metformin-oADM, indicating potential additive or synergistic effects within the combination metformin-GLP-1 RA group. Metformin-DPP-4i did not significantly improve renal impairment outcomes in this study.
通过评估肾功能损害与联合治疗之间的关联,对二甲双胍-胰高血糖素样肽-1受体激动剂(GLP-1 RA)、二甲双胍-二肽基肽酶-4抑制剂(DPP-4i)和二甲双胍-其他抗糖尿病药物(oADM)在糖尿病肾病(DKD)患者中的肾脏保护作用进行了比较。纳入了2010年1月1日至2017年1月1日期间最初诊断为DKD的患者。选择接受二甲双胍-GLP-1 RA、二甲双胍-DPP-4i或二甲双胍-oADM联合治疗的患者并进行配对。应用逻辑回归模型生成95%置信区间的比值比,以评估复合肾功能损害结局与联合抗糖尿病药物(ADM)组之间的关联。还进行了敏感性分析。在主要和次要分析中,接受二甲双胍-GLP-1 RA治疗的患者肾功能损害明显低于接受二甲双胍-DPP-4i治疗的患者(主要结局的OR为0.60,P<0.05;次要结局的OR为0.44,P<0.05)。在主要或次要分析中,二甲双胍-DPP-4i与二甲双胍-oADM相比,肾功能损害风险和ADM联合治疗之间的关联均无统计学意义(主要结局的OR = 1.22,P = 0.20;次要结局的OR = 0.90,P = 0.53)。敏感性分析结果与主要分析结果一致。与二甲双胍-DPP-4i和二甲双胍-oADM相比,二甲双胍-GLP-1 RA联合治疗的肾功能损害事件较少,表明二甲双胍-GLP-1 RA联合治疗组内可能存在相加或协同作用。在本研究中,二甲双胍-DPP-4i并未显著改善肾功能损害结局。