PMID- 27780736 OWN - NLM STAT- MEDLINE DCOM- 20171219 LR - 20180611 IS - 1873-5169 (Electronic) IS - 0196-9781 (Linking) VI - 86 DP - 2016 Dec TI - Add-on therapy with anagliptin in Japanese patients with type-2 diabetes mellitus treated with metformin and miglitol can maintain higher concentrations of biologically active GLP-1/total GIP and a lower concentration of leptin. PG - 118-125 LID - S0196-9781(16)30214-5 [pii] LID - 10.1016/j.peptides.2016.10.011 [doi] AB - Metformin, alpha-glucosidase inhibitors (alpha-GIs), and dipeptidyl peptidase 4 inhibitors (DPP-4Is) reduce hyperglycemia without excessive insulin secretion, and enhance postprandial plasma concentration of glucagon-like peptide-1 (GLP-1) in type-2 diabetes mellitus (T2DM) patients. We assessed add-on therapeutic effects of DPP-4I anagliptin in Japanese T2DM patients treated with metformin, an alpha-GI miglitol, or both drugs on postprandial responses of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP), and on plasma concentration of the appetite-suppressing hormone leptin. Forty-two Japanese T2DM patients with inadequately controlled disease (HbA1c: 6.5%-8.0%) treated with metformin (n=14), miglitol (n=14) or a combination of the two drugs (n=14) received additional treatment with anagliptin (100mg, p.o., b.i.d.) for 52 weeks. We assessed glycemic control, postprandial responses of GLP-1 and glucose-dependent insulinotropic polypeptide (GIP), and on plasma concentration of leptin in those patients. Add-on therapy with anagliptin for 52 weeks improved glycemic control and increased the area under the curve of biologically active GLP-1 concentration without altering obesity indicators. Total GIP concentration at 52 weeks was reduced by add-on therapy in groups treated with miglitol compared with those treated with metformin. Add-on therapy reduced leptin concentrations. Add-on therapy with anagliptin in Japanese T2DM patients treated with metformin and miglitol for 52 weeks improved glycemic control and enhanced postprandial concentrations of active GLP-1/total GIP, and reduce the leptin concentration. CI - Copyright A(c) 2016 Elsevier Inc. All rights reserved. FAU - Osonoi, Takeshi AU - Osonoi T AD - Naka Kinen Clinic, Ibaraki 311-0113, Japan. Electronic address: t-osonoi@kensei-kai.com. FAU - Saito, Miyoko AU - Saito M AD - Naka Kinen Clinic, Ibaraki 311-0113, Japan. FAU - Hariya, Natsuyo AU - Hariya N AD - Department of Epigenetic Medicine, Faculty of Medicine, University of Yamanashi, Yamanashi 409-3898, Japan. FAU - Goto, Moritaka AU - Goto M AD - Pharmaceutical Research Laboratories, Sanwa Kagaku Kenkyusho Co., Ltd., Mie 511-0406, Japan. FAU - Mochizuki, Kazuki AU - Mochizuki K AD - Laboratory of Food and Nutritional Sciences, Department of Local Produce and Food Sciences, Faculty of Life and Environmental Sciences, University of Yamanashi, Yamanashi 400-8510, Japan. Electronic address: mochizukik@yamanashi.ac.jp. LA - eng PT - Clinical Trial PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20161022 PL - United States TA - Peptides JT - Peptides JID - 8008690 RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) RN - 0 (Leptin) RN - 0 (Pyrimidines) RN - 0V5436JAQW (miglitol) RN - 19130-96-2 (1-Deoxynojirimycin) RN - 59392-49-3 (Gastric Inhibitory Polypeptide) RN - 89750-14-1 (Glucagon-Like Peptide 1) RN - 9100L32L2N (Metformin) RN - K726J96838 (anagliptin) SB - IM MH - 1-Deoxynojirimycin/*analogs & derivatives/pharmacology/therapeutic use MH - Aged MH - Blood Glucose MH - Diabetes Mellitus, Type 2/blood/*drug therapy MH - Drug Therapy, Combination MH - Female MH - Gastric Inhibitory Polypeptide/blood MH - Glucagon-Like Peptide 1/blood MH - Humans MH - Hypoglycemic Agents/pharmacology/*therapeutic use MH - Leptin/blood MH - Male MH - Metformin/pharmacology/*therapeutic use MH - Middle Aged MH - Pyrimidines/pharmacology/*therapeutic use MH - Treatment Outcome OTO - NOTNLM OT - &alpha OT - DPP-4I OT - GLP-1 OT - Metformin OT - Type-2 diabetes mellitus EDAT- 2016/10/27 06:00 MHDA- 2017/12/20 06:00 CRDT- 2016/10/27 06:00 PHST- 2016/07/08 00:00 [received] PHST- 2016/10/21 00:00 [revised] PHST- 2016/10/21 00:00 [accepted] PHST- 2016/10/27 06:00 [pubmed] PHST- 2017/12/20 06:00 [medline] PHST- 2016/10/27 06:00 [entrez] AID - S0196-9781(16)30214-5 [pii] AID - 10.1016/j.peptides.2016.10.011 [doi] PST - ppublish SO - Peptides. 2016 Dec;86:118-125. doi: 10.1016/j.peptides.2016.10.011. Epub 2016 Oct 22.