PMID- 32876863 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210118 IS - 1869-6953 (Print) IS - 1869-6961 (Electronic) IS - 1869-6961 (Linking) VI - 11 IP - 10 DP - 2020 Oct TI - Effect of Dipeptidyl Peptidase 4 Inhibitors Used in Combination with Insulin Treatment in Patients with Type 2 Diabetes: A Systematic Review and Meta-analysis. PG - 2371-2382 LID - 10.1007/s13300-020-00914-x [doi] AB - INTRODUCTION: To evaluate the efficacy and safety of dipeptidyl peptidase 4 inhibitors (DPP4i) used in combination with insulin in patients with type 2 diabetes mellitus (T2DM). METHODS: We searched the MEDLINE, Embase, and Cochrane library databases for randomized controlled trials (RCTs) published through June 2018. Studies with at least a 12-week treatment period were included to compare the addition of DPP4i to insulin with insulin control therapy. Meanwhile, groups on a stable insulin dosage (insulin-stable subgroup) or titrating insulin dosage (insulin-flexible subgroup) were analyzed separately. RESULTS: Twenty-one RCTs with 3697 patients randomized to a DPP4i/insulin treatment arm and 3538 to an insulin control arm were included. DPP4i, when added to insulin therapy, led to a significantly greater reduction in HbA1c (- 0.57%, 95% CI - 0.66, - 0.48) and provided significantly greater odds of achieving the HbA1c target < 7% (OR 3.45; 95% CI 2.58, 4.63). These effects were achieved in the context of a decrease in the daily insulin requirement, without increases in hypoglycemia risk and body weight, compared with the control treatment. Subgroup analysis showed control-adjusted reductions in HbA1c from baseline in the insulin-stable subgroup (- 0.64%; 95% CI - 0.74, - 0.53) and the insulin-flexible subgroup (- 0.43%; 95% CI - 0.56, - 0.30). Other results occurred similarly in both subgroups. CONCLUSIONS: The addition of DPP4i to insulin is associated with a statistically significant reduction in glycemic control as measured by HbA1c, fasting plasma glucose, and 2-h postprandial glucose, without increasing the risk of hypoglycemia and weight gain. These conclusions were also observed in both stable-dose and flexible-dose insulin subgroups. FAU - Yang, Jin AU - Yang J AD - Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing, China. FAU - Tian, Qing AU - Tian Q AD - Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing, China. FAU - Tang, Yuexin AU - Tang Y AD - MRL, Merck & Co., Inc., Kenilworth, NJ, USA. FAU - Shah, Arvind K AU - Shah AK AD - MRL, Merck & Co., Inc., Kenilworth, NJ, USA. FAU - Zhang, Ruya AU - Zhang R AD - Medical Affairs, MSD China Holding Co., Ltd., Shanghai, China. FAU - Chen, Guojuan AU - Chen G AD - Medical Affairs, MSD China Holding Co., Ltd., Shanghai, China. FAU - Zhang, Ye AU - Zhang Y AD - Medical Affairs, MSD China Holding Co., Ltd., Shanghai, China. FAU - Rajpathak, Swapnil AU - Rajpathak S AD - MRL, Merck & Co., Inc., Kenilworth, NJ, USA. swapnil.rajpathak@merck.com. FAU - Hong, Tianpei AU - Hong T AD - Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing, China. LA - eng PT - Journal Article DEP - 20200902 PL - United States TA - Diabetes Ther JT - Diabetes therapy : research, treatment and education of diabetes and related disorders JID - 101539025 PMC - PMC7509019 OTO - NOTNLM OT - Dipeptidyl peptidase 4 inhibitor OT - Insulin OT - Type 2 diabetes EDAT- 2020/09/03 06:00 MHDA- 2020/09/03 06:01 PMCR- 2020/09/02 CRDT- 2020/09/03 06:00 PHST- 2020/07/26 00:00 [received] PHST- 2020/09/03 06:00 [pubmed] PHST- 2020/09/03 06:01 [medline] PHST- 2020/09/03 06:00 [entrez] PHST- 2020/09/02 00:00 [pmc-release] AID - 10.1007/s13300-020-00914-x [pii] AID - 914 [pii] AID - 10.1007/s13300-020-00914-x [doi] PST - ppublish SO - Diabetes Ther. 2020 Oct;11(10):2371-2382. doi: 10.1007/s13300-020-00914-x. Epub 2020 Sep 2.