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Vildagliptin compared to glimepiride on post-prandial lipemia and on insulin resistance in type 2 diabetic patients.

AbstractOBJECTIVES:
To evaluate the effects of vildagliptin compared to glimepiride on glycemic control, insulin resistance and post-prandial lipemia.
MATERIAL AND METHODS:
167 type 2 diabetic patients, not adequately controlled by metformin, were randomized to vildagliptin 50 mg twice a day or glimepiride 2 mg three times a day for 6 months, in a double blind, randomized clinical trial. We evaluated: body mass index (BMI), glycemic control, fasting plasma insulin (FPI), homeostasis model assessment insulin resistance index (HOMA-IR), fasting plasma proinsulin (FPPr), glucagon, lipid profile, resistin, retinol binding protein-4 (RBP-4), visfatin and vaspin. Furthermore, at the randomization and at the end of the study all patients underwent an euglycemic hyperinsulinemic clamp to evaluate M value and an oral fat load.
RESULTS:
Despite a similar decrease of glycated hemoglobin, there were an increase of body weight with glimepiride + metformin and a decrease with vildagliptin + metformin. Fasting plasma insulin increased with glimepiride + metformin, while it did not change with vildagliptin + metformin. Vildagliptin + metformin improved lipid profile. Regarding insulin sensitivity, vildagliptin + metformin increased M value. Resistin, RBP-4, vaspin and visfatin were decreased by vildagliptin + metformin, but in group to group comparison, only vaspin reduction resulted statistically significant. Vildagliptin + metformin reduced post-prandial lipemia and insulinemia compared to glimepiride + metformin.
CONCLUSION:
Vildagliptin, in addition to metformin, was more effective than glimepiride + metformin in reducing insulin resistance and post-prandial lipemia.
AuthorsGiuseppe Derosa, Aldo Bonaventura, Lucio Bianchi, Davide Romano, Elena Fogari, Angela D'Angelo, Pamela Maffioli
JournalMetabolism: clinical and experimental (Metabolism) Vol. 63 Issue 7 Pg. 957-67 (Jul 2014) ISSN: 1532-8600 [Electronic] United States
PMID24874591 (Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial)
CopyrightCopyright © 2014 Elsevier Inc. All rights reserved.
Chemical References
  • Dipeptidyl-Peptidase IV Inhibitors
  • Hypoglycemic Agents
  • Hypolipidemic Agents
  • Nitriles
  • Pyrrolidines
  • Sulfonylurea Compounds
  • glimepiride
  • Metformin
  • Vildagliptin
  • Adamantane
Topics
  • Adamantane (adverse effects, analogs & derivatives, therapeutic use)
  • Aged
  • Diabetes Mellitus, Type 2 (blood, complications, drug therapy)
  • Dipeptidyl-Peptidase IV Inhibitors (adverse effects, therapeutic use)
  • Double-Blind Method
  • Drug Therapy, Combination (adverse effects)
  • Female
  • Humans
  • Hyperglycemia (prevention & control)
  • Hyperlipidemias (complications, prevention & control)
  • Hypoglycemia (chemically induced, prevention & control)
  • Hypoglycemic Agents (adverse effects, therapeutic use)
  • Hypolipidemic Agents (adverse effects, therapeutic use)
  • Insulin Resistance
  • Intention to Treat Analysis
  • Male
  • Metformin (adverse effects, therapeutic use)
  • Middle Aged
  • Nitriles (adverse effects, therapeutic use)
  • Postprandial Period
  • Pyrrolidines (adverse effects, therapeutic use)
  • Sulfonylurea Compounds (adverse effects, therapeutic use)
  • Vildagliptin
  • Weight Gain (drug effects)
  • Weight Loss (drug effects)

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