Abstract

ObjectiveTo 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.MethodsAll 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.ResultsThirteen 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.ConclusionsDPP-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.

Highlights

  • The prevalence of type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) is increasing steadily

  • Selected sulfonylureas are associated with a higher risk of hypoglycemia, which can be worse in CKD patients [4]

  • Insulin is used widely, its dose has to be adjusted occasionally based on blood glucose to avoid hypoglycemia because it is partially metabolized by the kidney [6]

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Summary

Introduction

The prevalence of type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) is increasing steadily. Diabetes is the leading cause of CKD, which might progress to end-stage renal disease and increase the risk of death [1]. Antihyperglycemic therapy, including the use of metformin, sulfonylureas, thiazolidinediones, and insulin, in T2DM patients with renal impairment remains controversial regarding its tolerability and safety. Selected sulfonylureas are associated with a higher risk of hypoglycemia, which can be worse in CKD patients [4]. There is no higher risk of hypoglycemia or dose adjustment in renal failure patients, they might cause fluid retention and edema, which are common manifestations of kidney disease [5]. Insulin is used widely, its dose has to be adjusted occasionally based on blood glucose to avoid hypoglycemia because it is partially metabolized by the kidney [6]

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