PMID- 32852696 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 - Efficacy and Safety of Sitagliptin Compared with Dapagliflozin in People >/= 65 Years Old with Type 2 Diabetes and Mild Renal Insufficiency. PG - 2419-2428 LID - 10.1007/s13300-020-00907-w [doi] AB - INTRODUCTION: Older patients with type 2 diabetes (T2D) are at increased risk of diabetic nephropathy and mild renal insufficiency. This analysis compared the anti-hyperglycemic efficacy and safety of sitagliptin with dapagliflozin in patients >/= 65 years of age with T2D and mild renal insufficiency. METHODS: This was a post hoc analysis of data from 410 patients >/= 65 years old who participated in a 24-week, randomized, double-blind clinical trial (CompoSIT-R [comparison of sitagliptin with dapagliflozin in mild renal impairment]; NCT02532855) in T2D patients with mild renal insufficiency and on metformin +/- a sulfonylurea; the primary efficacy end point was change in HbA1c at week 24. RESULTS: Treatment groups were well balanced at baseline (mean HbA1c = 7.7/7.7% and eGFR = 79/76 ml/min/1.73 m(2) for sitagliptin/dapagliflozin). At week 24, LS mean (95% CI) change in HbA1c and percentage of patients with HbA1c < 7% were greater with sitagliptin, - 0.48% and 41%, respectively, compared with dapagliflozin, - 0.36% and 28%; between-group differences = - 0.12% (- 0.36, 0.01) and 12.8% (3.3, 22.2) for change in HbA1c and percentage with HbA1c < 7%, respectively. The sitagliptin group had greater reductions in PPG end points, while the dapagliflozin group had greater reductions in FPG. Treatments were generally well tolerated. There were fewer drug-related adverse events (AEs) with sitagliptin than with dapagliflozin but AE profiles were otherwise similar. CONCLUSIONS: In patients >/= 65 years of age with T2D and mild renal insufficiency with inadequate glycemic control on metformin +/- sulfonylurea, treatment with sitagliptin for 24 weeks resulted in improvement in HbA1c relative to treatment with dapagliflozin that is consistent with that previously observed in the overall population. Both treatments were generally well tolerated. FAU - Raji, Annaswamy AU - Raji A AUID- ORCID: 0000-0002-2430-8160 AD - Merck & Co., Inc., Kenilworth, NJ, USA. annaswamy.raji@merck.com. FAU - Xu, Zhi Jin AU - Xu ZJ AD - Merck & Co., Inc., Kenilworth, NJ, USA. FAU - Lam, Raymond L H AU - Lam RLH AD - Merck & Co., Inc., Kenilworth, NJ, USA. FAU - O'Neill, Edward A AU - O'Neill EA AD - Merck & Co., Inc., Kenilworth, NJ, USA. FAU - Kaufman, Keith D AU - Kaufman KD AD - Merck & Co., Inc., Kenilworth, NJ, USA. FAU - Engel, Samuel S AU - Engel SS AUID- ORCID: 0000-0002-4439-6356 AD - Merck & Co., Inc., Kenilworth, NJ, USA. LA - eng PT - Journal Article DEP - 20200827 PL - United States TA - Diabetes Ther JT - Diabetes therapy : research, treatment and education of diabetes and related disorders JID - 101539025 PMC - PMC7509009 OTO - NOTNLM OT - DPP-4 OT - Elderly OT - Incretins OT - SGLT2 EDAT- 2020/08/28 06:00 MHDA- 2020/08/28 06:01 PMCR- 2020/08/27 CRDT- 2020/08/28 06:00 PHST- 2020/07/15 00:00 [received] PHST- 2020/08/28 06:00 [pubmed] PHST- 2020/08/28 06:01 [medline] PHST- 2020/08/28 06:00 [entrez] PHST- 2020/08/27 00:00 [pmc-release] AID - 10.1007/s13300-020-00907-w [pii] AID - 907 [pii] AID - 10.1007/s13300-020-00907-w [doi] PST - ppublish SO - Diabetes Ther. 2020 Oct;11(10):2419-2428. doi: 10.1007/s13300-020-00907-w. Epub 2020 Aug 27.