PMID- 23630415 OWN - NLM STAT- MEDLINE DCOM- 20131126 LR - 20221207 IS - 1177-8881 (Electronic) IS - 1177-8881 (Linking) VI - 7 DP - 2013 TI - Effects of vildagliptin (Galvus(R)) therapy in patients with type 2 diabetes mellitus after heart transplantation. PG - 297-303 LID - 10.2147/DDDT.S43092 [doi] AB - BACKGROUND: Type 2 Diabetes mellitus (T2DM) is a common comorbidity in patients after heart transplantation (HTx) and is associated with adverse long-term outcomes. METHODS: The retrospective study reported here analyzed the effects of vildagliptin therapy in stable patients post-HTx with T2DM and compared these with control patients for matched-pairs analysis. A total of 30 stable patients post-HTx with T2DM were included in the study. Fifteen patients (mean age 58.6 +/- 6.0 years, mean time post-HTx 4.9 +/- 5.3 years, twelve male and three female) were included in the vildagliptin group (VG) and 15 patients were included in the control group (CG) (mean age 61.2 +/- 8.3 years, mean time post-HTx 7.2 +/- 6.6 years, all male). RESULTS: Mean glycated hemoglobin (HbA1c) in the VG was 7.4% +/- 0.7% before versus 6.8% +/- 0.8% after 8 months of vildagliptin therapy (P = 0.002 vs baseline). In the CG, HbA1c was 7.0% +/- 0.7% versus 7.3% +/- 1.2% at follow-up (P = 0.21). Additionally, there was a significant reduction in mean blood glucose in the VG, from 165.0 +/- 18.8 mg/dL to 147.9 +/- 22.7 mg/dL (P = 0.002 vs baseline), whereas mean blood glucose increased slightly in the CG from 154.7 +/- 19.7 mg/dL to 162.6 +/- 35.0 mg/dL (P = 0.21). No statistically significant changes in body weight (from 83.3 +/- 10.8 kg to 82.0 +/- 10.9 kg, P = 0.20), total cholesterol (1.5%, P = 0.68), or triglyceride levels (8.0%, P = 0.65) were seen in the VG. No significant changes in immunosuppressive drug levels or dosages were observed in either group. CONCLUSION: Vildagliptin therapy significantly reduced HbA1c and mean blood glucose levels in post-HTx patients in this study with T2DM and did not have any negative effects on lipid profile or body weight. Thus, vildagliptin therapy presented an interesting therapeutic approach for this selected patient cohort. FAU - Gueler, Ibrahim AU - Gueler I AD - Department of Cardiology, University of Heidelberg, Heidelberg, Germany. FAU - Mueller, Susanne AU - Mueller S FAU - Helmschrott, Matthias AU - Helmschrott M FAU - Oeing, Christian U AU - Oeing CU FAU - Erbel, Christian AU - Erbel C FAU - Frankenstein, Lutz AU - Frankenstein L FAU - Gleissner, Christian AU - Gleissner C FAU - Ruhparwar, Arjang AU - Ruhparwar A FAU - Ehlermann, Philipp AU - Ehlermann P FAU - Dengler, Thomas J AU - Dengler TJ FAU - Katus, Hugo A AU - Katus HA FAU - Doesch, Andreas O AU - Doesch AO LA - eng PT - Journal Article DEP - 20130408 PL - New Zealand TA - Drug Des Devel Ther JT - Drug design, development and therapy JID - 101475745 RN - 0 (Blood Glucose) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Glycated Hemoglobin A) RN - 0 (Immunosuppressive Agents) RN - 0 (Lipids) RN - 0 (Nitriles) RN - 0 (Pyrrolidines) RN - 0 (hemoglobin A1c protein, human) RN - I6B4B2U96P (Vildagliptin) RN - PJY633525U (Adamantane) SB - IM MH - Adamantane/adverse effects/*analogs & derivatives/therapeutic use MH - Aged MH - Blood Glucose/analysis MH - Body Weight/drug effects MH - Diabetes Mellitus, Type 2/blood/*drug therapy MH - Dipeptidyl-Peptidase IV Inhibitors/*therapeutic use MH - Female MH - Glycated Hemoglobin/analysis MH - Heart Transplantation/*adverse effects MH - Humans MH - Immunosuppressive Agents/therapeutic use MH - Lipids/blood MH - Male MH - Middle Aged MH - Nitriles/adverse effects/*therapeutic use MH - Pyrrolidines/adverse effects/*therapeutic use MH - Retrospective Studies MH - Vildagliptin PMC - PMC3623547 OTO - NOTNLM OT - glycated hemoglobin OT - immunosuppression OT - mean blood glucose EDAT- 2013/05/01 06:00 MHDA- 2013/12/16 06:00 PMCR- 2013/04/08 CRDT- 2013/05/01 06:00 PHST- 2013/05/01 06:00 [entrez] PHST- 2013/05/01 06:00 [pubmed] PHST- 2013/12/16 06:00 [medline] PHST- 2013/04/08 00:00 [pmc-release] AID - dddt-7-297 [pii] AID - 10.2147/DDDT.S43092 [doi] PST - epublish SO - Drug Des Devel Ther. 2013 Apr 8;7:297-303. doi: 10.2147/DDDT.S43092. Print 2013.