Key result
Glimepiride significantly improved insulin resistance (HOMA-IR), increased adiponectin, and reduced inflammatory cytokines and atherosclerotic parameters compared to glibenclamide over 28 weeks.
Why the study?
Does glimepiride improve insulin resistance and surrogate markers of atherosclerosis in patients with type 2 diabetes mellitus compared to glibenclamide or insulin?
RCT (n=46)
Open-label
Randomly divided into two groups
No
Does glimepiride improve insulin resistance and surrogate markers of atherosclerosis in patients with type 2 diabetes mellitus compared to glibenclamide or insulin?
Switching from glibenclamide to glimepiride in patients with type 2 diabetes improves insulin resistance, inflammatory cytokines, and surrogate markers of atherosclerosis.
May favor glimepiride over glibenclamide in T2DM for metabolic and inflammatory benefits; extends RCT evidence on sulfonylurea differences in surrogate CV markers.
BACKGROUND: Plasma adiponectin levels increase after the administration of glimepiride. This unique effects would also be expected to improve other adipocytokines and have anti-atherosclerotic action in patients with metabolic syndrome. METHODS: Thirty-four patients with type 2 diabetes mellitus who were administrated glibenclamide were randomly divided into two groups. In 20 patients glibenclamide was changed to glimepiride (GP group), and the administration of glibenclamide (GB group) was continued in 14 patients. Twelve patients receiving insulin therapy (INS group) were enrolled for comparison. The levels of plasma adiponectin, high sensitive-CRP, TNF-alpha, interleukin-6, homeostasis model assessment-insulin resistance (HOMA-IR), brachial-ankle pulse wave velocity (baPWV) and augmentation index (AI) were measured before and 28 weeks after the therapy. RESULTS: HOMA-IR in the GP group was significantly decreased compared to the GB group. Plasma adiponectin levels were significantly increased in the GP group but not in the other groups. TNF-alpha, interleukin-6 and high sensitive-CRP levels were significantly decreased in the GP group, but not in the other groups. The baPWV and AI levels did not change in either the GB or the INS group, but were significantly decreased in the GP group. CONCLUSIONS: Glimepiride appears to improve insulin resistance and atherosclerotic disorders.
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Koshiba et al. (2006) conducted an RCT in Type 2 diabetes mellitus (n=46). Glimepiride vs. Glibenclamide or insulin therapy was evaluated on HOMA-IR at 28 weeks (p=<0.01). Glimepiride significantly improved insulin resistance (HOMA-IR), increased adiponectin, and reduced inflammatory cytokines and atherosclerotic parameters compared to glibenclamide over 28 weeks.
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