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二肽基肽酶IV抑制剂用于慢性肾脏病糖尿病患者的疗效与安全性:一项随机临床试验的荟萃分析

Efficacy and Safety of the Utilization of Dipeptidyl Peptidase IV Inhibitors in Diabetic Patients with Chronic Kidney Disease: A Meta-Analysis of Randomized Clinical Trials.

作者信息

Mahzari Moeber M, Alqirnas Muhannad Qirnas, Alhamadh Moustafa S, Alrasheed Faisal, Alhabeeb Abdulrahman Yousef, Al Madani Wedad, Aldera Hussain

机构信息

College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.

出版信息

Diabetes Metab Syndr Obes. 2024 Mar 23;17:1425-1440. doi: 10.2147/DMSO.S445114. eCollection 2024.

Abstract

AIM

To assess the efficacy and safety of Dipeptidyl Peptidase IV (DPP-4) inhibitors in patients with Type-2 Diabetes Mellitus (T2DM) and chronic kidney disease (CKD) using level 1 evidence.

METHODS

The Cochrane and PubMed databases were searched from inception until January 1, 2022. RCTs that studied the efficacy and safety of DPP-4 inhibitors in diabetic patients with CKD were included. The primary efficacy outcome was assessed as the mean difference between HbA1c at the beginning and the end of each study for each arm, and the primary safety outcome was assessed as the incidence of adverse events and severe adverse events in each study.

RESULTS

Twenty-one studies satisfied the pre-defined eligibility criteria. In assessing the efficacy of DPP-4 inhibitors in the treatment of T2DM and CKD, a total of 2917 patients under the DPP-4 inhibitors group and 2377 patients under the control group were included; The mean difference between the HbA1c of DPP-4 Inhibitor and the control group was -0.5295 with a 95% CI of -0.5337 to -0.5252. The included studies had high heterogeneity p < 0.00001 and I = 99%. In assessing the safety outcome and tolerability of DPP-4 inhibitors, a total of 8138 patients under the DPP-4 inhibitors group and 7517 patients under the control group were included; the odds ratio of adverse events between both groups was 0.9967 with a 95% CI of 0.9967 to 1.1047. The included studies had low heterogeneity p = 0.25 and I = 15%. The overall effect, Z = 0.06 (p = 0.95), was insignificant.

CONCLUSION

Patients suffering from both T2DM and CKD exhibited a significantly enhanced glycemic control when treated with DPP-4 inhibitors in comparison to the control group. Furthermore, no significant difference in the incidence of adverse events was observed between the DPP-4 inhibitors and the control group.

摘要

目的

采用一级证据评估二肽基肽酶IV(DPP-4)抑制剂在2型糖尿病(T2DM)合并慢性肾脏病(CKD)患者中的疗效和安全性。

方法

检索Cochrane数据库和PubMed数据库自建库至2022年1月1日的文献。纳入研究DPP-4抑制剂在糖尿病合并CKD患者中疗效和安全性的随机对照试验(RCT)。主要疗效结局评估为各研究中每组治疗开始和结束时糖化血红蛋白(HbA1c)的平均差值,主要安全性结局评估为各研究中不良事件和严重不良事件的发生率。

结果

21项研究符合预先设定的纳入标准。在评估DPP-4抑制剂治疗T2DM合并CKD的疗效时,DPP-4抑制剂组共纳入2917例患者,对照组共纳入2377例患者;DPP-4抑制剂组与对照组HbA1c的平均差值为-0.5295,95%置信区间为-0.5337至-0.5252。纳入研究具有高度异质性(p<0.00001,I=99%)。在评估DPP-4抑制剂的安全性结局和耐受性时,DPP-4抑制剂组共纳入8138例患者,对照组共纳入7517例患者;两组不良事件的比值比为0.9967,95%置信区间为0.9967至1.1047。纳入研究具有低度异质性(p=0.25,I=15%)。总体效应Z=0.06(p=0.95),无统计学意义。

结论

与对照组相比,DPP-4抑制剂治疗T2DM合并CKD患者时血糖控制显著增强。此外,DPP-4抑制剂组与对照组在不良事件发生率上无显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95e/10968002/54d75b15a0bc/DMSO-17-1425-g0001.jpg

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