PMID- 27512877 OWN - NLM STAT- MEDLINE DCOM- 20170206 LR - 20221207 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 95 IP - 32 DP - 2016 Aug TI - Efficacy of different dipeptidyl peptidase-4 (DPP-4) inhibitors on metabolic parameters in patients with type 2 diabetes undergoing dialysis. PG - e4543 LID - 10.1097/MD.0000000000004543 [doi] LID - e4543 AB - Hyperglycemia is associated with increased mortality and morbidity in patients with type 2 diabetes mellitus (T2DM) who are undergoing dialysis. Although dipeptidyl peptidase-4 (DPP-4) inhibitors have been widely used in end-stage renal disease (ESRD) patients with T2DM, there are few studies on their efficacy in this population. We studied the effect of 3 different DPP-4 inhibitors on metabolic parameters in ESRD patients with T2DM.Two hundred ESRD patients with T2DM who were treated with DPP-4 inhibitors (sitagliptin, vildagliptin, or linagliptin) were enrolled and analyzed retrospectively. The changes in glycated hemoglobin (HbA1c), fasting plasma glucose, and lipid profiles were assessed before and after 3 months of treatment with DPP-4 inhibitors. Subgroup analysis was done for each hemodialysis (HD) and peritoneal dialysis (PD) group.There was no significant difference in the decrease in the HbA1c level among sitagliptin, vildagliptin, and linagliptin treatment groups (-0.74 +/- 1.57, -0.39 +/- 1.45, and -0.08 +/- 1.40, respectively, P = 0.076). The changes in fasting blood glucose and lipid profiles were also not significantly different. In HD patients (n = 115), there was no difference in the HbA1c level among the 3 groups. In contrast, in PD patients (n = 85), HbA1c was reduced more after 3 months of treatment with sitagliptin compared with vildagliptin and linagliptin (-1.58 +/- 0.95, -0.46 +/- 0.98, -0.04 +/- 1.22, respectively, P = 0.001).There was no significant difference in the glucose-lowering effect between the different DPP-4 inhibitors tested in ESRD patients. In PD patients, sitagliptin tends to lower the HbA1c level more than the other inhibitors. The glucose-lowering efficacy of the 3 DPP-4 inhibitors was comparable. FAU - Park, Se Hee AU - Park SH AD - Division of Endocrinology and Metabolism, Department of Internal Medicine Department of Medicine, The Graduate School, Yonsei University College of Medicine, Seoul Division of Endocrinology and Metabolism, Department of Internal Medicine, National Health Insurance Service Ilsan Hospital, Goyang, Gyeonggi Division of Nephrology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul Division of Endocrinology and Metabolism, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea. FAU - Nam, Joo Young AU - Nam JY FAU - Han, Eugene AU - Han E FAU - Lee, Yong-Ho AU - Lee YH FAU - Lee, Byung-Wan AU - Lee BW FAU - Kim, Beom Seok AU - Kim BS FAU - Cha, Bong-Soo AU - Cha BS FAU - Kim, Chul Sik AU - Kim CS FAU - Kang, Eun Seok AU - Kang ES LA - eng PT - Journal Article PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Blood Glucose) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Glycated Hemoglobin A) RN - 0 (Lipids) RN - 0 (Nitriles) RN - 0 (Pyrrolidines) RN - 0 (hemoglobin A1c protein, human) RN - 3X29ZEJ4R2 (Linagliptin) RN - I6B4B2U96P (Vildagliptin) RN - PJY633525U (Adamantane) RN - TS63EW8X6F (Sitagliptin Phosphate) SB - IM MH - Adamantane/analogs & derivatives/therapeutic use MH - Blood Glucose/analysis MH - Diabetes Mellitus, Type 2/complications/*drug therapy/metabolism MH - Diabetic Nephropathies/therapy MH - Dipeptidyl-Peptidase IV Inhibitors/*therapeutic use MH - Female MH - Glycated Hemoglobin/analysis MH - Humans MH - Kidney Failure, Chronic/etiology/therapy MH - Linagliptin/therapeutic use MH - Lipids/blood MH - Male MH - Middle Aged MH - Nitriles/therapeutic use MH - Peritoneal Dialysis MH - Pyrrolidines/therapeutic use MH - Renal Dialysis MH - Retrospective Studies MH - Sitagliptin Phosphate/therapeutic use MH - Treatment Outcome MH - Vildagliptin PMC - PMC4985332 COIS- The authors have no funding and conflicts of interest to disclose. EDAT- 2016/08/12 06:00 MHDA- 2017/02/07 06:00 PMCR- 2016/08/12 CRDT- 2016/08/12 06:00 PHST- 2016/08/12 06:00 [entrez] PHST- 2016/08/12 06:00 [pubmed] PHST- 2017/02/07 06:00 [medline] PHST- 2016/08/12 00:00 [pmc-release] AID - 00005792-201608090-00043 [pii] AID - 10.1097/MD.0000000000004543 [doi] PST - ppublish SO - Medicine (Baltimore). 2016 Aug;95(32):e4543. doi: 10.1097/MD.0000000000004543.