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二肽基肽酶-4抑制剂在中重度肾功能不全2型糖尿病患者中的疗效与安全性:一项系统评价和荟萃分析

Efficacy and safety of dipeptidyl peptidase-4 inhibitors in type 2 diabetes mellitus patients with moderate to severe renal impairment: a systematic review and meta-analysis.

作者信息

Cheng Dongsheng, Fei Yang, Liu Yumei, Li Junhui, Chen Yuqiang, Wang Xiaoxia, Wang Niansong

机构信息

Department of Nephrology and Rheumatology, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, P.R. China.

出版信息

PLoS One. 2014 Oct 31;9(10):e111543. doi: 10.1371/journal.pone.0111543. eCollection 2014.

Abstract

OBJECTIVE

To perform a systematic review and meta-analysis regarding the efficacy and safety of dipeptidyl peptidase-4 (DDP-4) inhibitors ("gliptins") for the treatment of type 2 diabetes mellitus (T2DM) patients with moderate to severe renal impairment.

METHODS

All available randomized-controlled trials (RCTs) that assessed the efficacy and safety of DDP-4 inhibitors compared with placebo, no treatment, or active drugs were identified using PubMed, EMBASE, Cochrane CENTRAL, conference abstracts, clinical trials.gov, pharmaceutical company websites, the FDA, and the EMA (up to June 2014). Two independent reviewers extracted the data, and a random-effects model was applied to estimate summary effects.

RESULTS

Thirteen reports of ten studies with a total of 1,915 participants were included in the final analysis. Compared with placebo or no treatment, DPP-4 inhibitors reduced HbA1c significantly (-0.52%, 95%CI -0.64 to -0.39) and had no increased risk of hypoglycemia (RR 1.10, 95%CI 0.92 to 1.32) or weight gain. In contrast to glipizide monotherapy, DPP-4 inhibitors showed no difference in HbA1c lowering effect (-0.08%, 95% CI -0.40 to 0.25) but had a lower incidence of hypoglycemia (RR 0.40, 95%CI 0.23 to 0.69). Furthermore, DPP-4 inhibitors were well-tolerated, without any additional mortality and adverse events. However, the quality of evidence was mostly as low, as assessed using the GRADE system for each outcome.

CONCLUSIONS

DPP-4 inhibitors are effective at lowering HbA1c in T2DM patients with moderate to severe renal impairment. DPP-4 inhibitors also have a potential advantage in lowering the risk of adverse events. Regarding the low quality of the evidence according to GRADE, additional well-designed randomized trials that focus on the safety and efficacy of DPP-4 inhibitors in various CKD stages are needed urgently.

摘要

目的

对二肽基肽酶-4(DPP-4)抑制剂(“格列汀类”)治疗中度至重度肾功能损害的2型糖尿病(T2DM)患者的疗效和安全性进行系统评价和荟萃分析。

方法

通过PubMed、EMBASE、Cochrane CENTRAL、会议摘要、clinicaltrials.gov、制药公司网站、美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)(截至2014年6月)检索所有评估DPP-4抑制剂与安慰剂、未治疗或活性药物相比疗效和安全性的随机对照试验(RCT)。两名独立的研究者提取数据,并采用随机效应模型估计汇总效应。

结果

最终分析纳入了10项研究的13份报告,共1915名参与者。与安慰剂或未治疗相比,DPP-4抑制剂显著降低糖化血红蛋白(HbA1c)(-0.52%,95%置信区间为-0.64至-0.39),且低血糖风险(风险比1.10,95%置信区间为0.92至1.32)或体重增加风险未增加。与格列吡嗪单药治疗相比,DPP-4抑制剂在降低HbA1c效果方面无差异(-0.08%,95%置信区间为-0.40至0.25),但低血糖发生率较低(风险比0.40,95%置信区间为0.23至0.69)。此外,DPP-4抑制剂耐受性良好,无额外的死亡率和不良事件。然而,使用GRADE系统对每个结局评估时,证据质量大多较低。

结论

DPP-4抑制剂对降低中度至重度肾功能损害的T2DM患者的HbA1c有效。DPP-4抑制剂在降低不良事件风险方面也具有潜在优势。鉴于根据GRADE评估证据质量较低,迫切需要开展更多精心设计的随机试验,关注DPP-4抑制剂在不同慢性肾脏病阶段的安全性和疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f14/4216116/ff5538965e87/pone.0111543.g001.jpg

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