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钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂、胰高血糖素样肽-1(GLP-1)受体激动剂和非奈利酮在2型糖尿病合并非透析慢性肾脏病中的临床疗效和安全性:一项随机临床试验的网状Meta分析

Clinical efficacy and safety of sodium-glucose cotransporter protein-2 (SGLT-2) inhibitor, glucagon-like peptide-1 (GLP-1) receptor agonist, and Finerenone in type 2 diabetes mellitus with non-dialysis chronic kidney disease: a network meta-analysis of randomized clinical trials.

作者信息

Guo Jingyi, Wei Maoying, Zhang Wenhua, Jiang Yijia, Li Aijing, Wang Churan, Yin Dan, Sun Anning, Gong Yanbing

机构信息

Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Pharmacol. 2025 Mar 27;16:1517272. doi: 10.3389/fphar.2025.1517272. eCollection 2025.

Abstract

OBJECTIVE

To investigate the safety and clinical efficacy of sodium-glucose cotransporter protein-2 (SGLT-2) inhibitors, glucagon-like peptide-1 (GLP-1) receptor agonists and Finerenone in treating patients with type 2 diabetes mellitus (T2DM) combined with non-dialysis chronic kidney disease (CKD).

METHODS

Cochrane Library, PubMed, EMBASE, Web of Science, CNKI, CQVIP database, and WanFang from their inception up to November 2023 were searched to compare the efficacy and safety of SGLT-2 inhibitors, GLP-1 RA receptor agonists and Finerenone in the treatment of T2DM patients with non-dialysis CKD. To assess the methodological quality and risk of bias in the included studies, we utilized the Cochrane Risk of Bias Assessment tool (RoB 2.0). The confidence of evidence was examined using Confidence in Network Meta-Analysis (CINeMA). Traditional meta-analysis of variables was conducted using Stata 17.0 software with a random-effects model. We assessed publication bias using funnel plots and explored potential sources of heterogeneity through subgroup analysis.

RESULTS

A total of 39 studies (99,599 patients) were included. Compared to Placebo (PBO), SGLT-2 inhibitors demonstrated superior efficacy in reducing glycosylated hemoglobin (HbA1c) (MD = -0.33; 95%CI: from -0.52 to -0.15), systolic blood pressure (SBP) (MD from -5.52 to -1.50; 95%CI from -8.80 to -0.23), body weight (MD from -3.81 to -1.29; 95%CI from -6.34 to -0.84) and diastolic blood pressure (DBP) (MD = -1.86; 95%CI: -3.18, -40.54). The efficacy of Liraglutide in reducing Low-Density Lipoprotein Cholesterol (LDL-C) surpassed that of other agents (MD from -1.58 to -1.41; 95%CI from -2.05 to -0.81). Finerenone significantly reduced SBP (MD = -1.65; 95%CI: -2.48, -0.81) compared to PBO. According to the SUCRA based relative ranking of treatments, Empagliflozin was the most effective in reducing HbA1c and DBP. Semaglutide was the least harmful to estimated glomerular filtration rate. Liraglutide was the most effective in reducing LDL-C. Bexagliflozin, Canagliflozin were the most effective in reducing SBP and body weight. Finerenone had the lowest incidence of urinary tract infection, Hypoglycemia was the lowest in the Luseogliflozin group. Ertugliflozin was the least likely to cause acute kidney injury. Canagliflozin had the lowest probability of any adverse event.

CONCLUSION

The safety of these drugs has been confirmed, except for some special drugs. SGLT-2 inhibitors had a preferential glucose-lowering and weight-loss function, GLP-1 receptor agonists had a preferential lowering of LDL-C and blood glucose, and Finereone significantly reduced SBP compared with PBO. Systematic Review Registration: PROSPERO, CRD42024571544.

摘要

目的

探讨钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂、胰高血糖素样肽-1(GLP-1)受体激动剂和非奈利酮治疗2型糖尿病(T2DM)合并非透析慢性肾脏病(CKD)患者的安全性和临床疗效。

方法

检索Cochrane图书馆、PubMed、EMBASE、Web of Science、中国知网、维普数据库和万方数据库,检索时间从建库至2023年11月,以比较SGLT-2抑制剂、GLP-1受体激动剂和非奈利酮治疗T2DM合并非透析CKD患者的疗效和安全性。为评估纳入研究的方法学质量和偏倚风险,我们使用了Cochrane偏倚风险评估工具(RoB 2.0)。使用网络Meta分析的信心(CINeMA)来检验证据的可信度。使用Stata 17.0软件采用随机效应模型对变量进行传统Meta分析。我们使用漏斗图评估发表偏倚,并通过亚组分析探索异质性的潜在来源。

结果

共纳入39项研究(99599例患者)。与安慰剂(PBO)相比,SGLT-2抑制剂在降低糖化血红蛋白(HbA1c)(MD=-0.33;95%CI:-0.52至-0.15)、收缩压(SBP)(MD为-5.52至-1.50;95%CI为-8.80至-0.23)、体重(MD为-3.81至-1.29;95%CI为-6.34至-0.84)和舒张压(DBP)(MD=-1.86;95%CI:-3.18,-40.54)方面显示出更好的疗效。利拉鲁肽在降低低密度脂蛋白胆固醇(LDL-C)方面的疗效超过其他药物(MD为-1.58至-1.41;95%CI为-2.05至-0.81)。与PBO相比,非奈利酮显著降低SBP(MD=-1.65;95%CI:-2.48,-0.81)。根据基于累积排序曲线下面积(SUCRA)的治疗相对排名,恩格列净在降低HbA1c和DBP方面最有效。司美格鲁肽对估计肾小球滤过率的损害最小。利拉鲁肽在降低LDL-C方面最有效。贝西格列净、卡格列净在降低SBP和体重方面最有效。非奈利酮的尿路感染发生率最低,卢西格列净组的低血糖发生率最低。依鲁格列净导致急性肾损伤的可能性最小。卡格列净发生任何不良事件的概率最低。

结论

除某些特殊药物外,这些药物的安全性已得到证实。SGLT-2抑制剂具有优先的降糖和减重作用,GLP-1受体激动剂具有优先降低LDL-C和血糖的作用,与PBO相比,非奈利酮显著降低SBP。系统评价注册:PROSPERO,CRD42024571544。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a2/11983143/4a36aa173b10/fphar-16-1517272-g001.jpg

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