Effect of acarbose, an alpha-glucosidase inhibitor, on serum lipoprotein lipase mass levels and common carotid artery intima-media thickness in type 2 diabetes mellitus treated by sulfonylurea

J Atheroscler Thromb. 2008 Jun;15(3):154-9. doi: 10.5551/jat.e549.

Abstract

Aim: Previous reports indicate that serum lipoprotein lipase mass levels (LPL mass) and common carotid artery intima-media thickness (CCA-IMT) are independent predictors of atherosclerotic diseases. The aim of this study was to examine the effects of combination therapy of sulfonylurea and acarbose on LPL mass and CCA-IMT.

Methods: Eighty-four patients with type 2 diabetes mellitus, who were treated with only sulfonylureas and showed CCA-IMT of more than 0.9 mm at baseline, were selected and randomly divided into two groups. One group was administered acarbose 300 mg/day for 12 months (acarbose group, n=41), and the other group was not administered acarbose (non-acarbose group, n=43).

Results: After 12 months, a significant increase in LPL mass and a significant decrease in CCA-IMT were observed in the acarbose group (1.024 to 0.964 mm), but no significant changes were observed in the non-acarbose group. In a subgroup analysis of patients with HbA1c improved by 0.5% or more, the increase of LPL mass and decrease of CCA-IMT was significantly greater in the acarbose group than in the non-acarbose group although the changes in HbA1c were similar in two groups.

Conclusions: We concluded that reducing postprandial hyperglycemia might increase LPL mass levels and might be useful to prevent macroangiopathy in type 2 diabetic patients treated by sulfonylurea.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Acarbose / pharmacology*
  • Aged
  • Body Weight
  • Carotid Arteries / metabolism*
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Female
  • Glycoside Hydrolase Inhibitors*
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Lipoprotein Lipase / blood*
  • Male
  • Middle Aged
  • Sulfonylurea Compounds / pharmacology*
  • Tunica Intima / pathology*
  • Tunica Media / pathology*

Substances

  • Glycoside Hydrolase Inhibitors
  • Hypoglycemic Agents
  • Sulfonylurea Compounds
  • Lipoprotein Lipase
  • Acarbose