Key result
Repaglinide improves brachial reactivity and reduces oxidative stress vs glibenclamide in type 2 diabetes.
Why the study?
Endothelial dysfunction contributes to diabetic mortality and postprandial hyperglycemia may promote atherogenesis, but effects of short- versus long-acting insulin secretagogues on endothelial function in type 2 diabetes were unclear.
Does repaglinide improve brachial reactivity compared to glibenclamide in type 2 diabetic patients with poor glucose control?
RCT (n=16)
randomized, cross-over
Does repaglinide improve brachial reactivity compared to glibenclamide in type 2 diabetic patients with poor glucose control?
p-value: p=<0.003
Repaglinide improves endothelial function and reduces oxidative stress in type 2 diabetic patients, likely through better control of postprandial glucose levels.
Repaglinide may improve endothelial function in type 2 diabetes via postprandial control; leaves open preference over glibenclamide pending larger trials.
OBJECTIVE: Several studies have demonstrated that endothelial dysfunction plays a central role in diabetic mortality and that the prooxidative effect of postprandial hyperglycemia may actively contribute to atherogenesis. Thus, we investigated the possible effect of short-acting (repaglinide) and long-acting (glibenclamide) insulin secretagogues on endothelial function in type 2 diabetic patients. RESEARCH DESIGN AND METHODS: Sixteen type 2 diabetic patients undergoing diet treatment and with poor glucose control volunteered for the study. The study was designed as a 4-month, randomized, cross-over, parallel-group trial of repaglinide (1 mg twice a day) versus glibenclamide (5 mg twice a day). All patients underwent the following investigations: 1) anthropometrics determinations, 2) blood sampling for routine laboratory analyses and for assessment of oxidative stress indexes, and 3) a brachial reactivity test to evaluate the endothelial function through the study of arterial diameter and flow changes with and without intraarterial infusion of N(G)-monomethyl-l-arginine, an inhibitor of nitric oxide synthase and tetraethylammonium chloride (TEA), a Ca(2+)-activated K(+) (K(Ca)) channel blocker. All patients were randomly assigned to receive repaglinide or glibenclamide for a period of 4 weeks. RESULTS: Repaglinide administration was associated with a significant reduction in 2-h plasma glucose levels (P < 0.001) and in plasma thiobarbituric acid-reactive substances (TBARS) concentrations (P < 0.001) and with a significant increase in plasma antioxidant power, assessed as Trolox equivalent antioxidant capacity (TEAC) (P < 0.001), effects not observed after glibenclamide administration. With regard to brachial reactivity parameters, repaglinide but not glibenclamide was associated with a significant improvement in brachial reactivity parameters (P < 0.003 for all parameters). In contrast, intra-arterial infusion of L-NMMA and TEA reduced the beneficial effect of repaglinide. CONCLUSIONS: Repaglinide administration, through good control of postprandial glucose levels, improves brachial reactivity and declines oxidative stress indexes.
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Manzella et al. (2005) conducted an RCT in Type 2 diabetes (n=16). Repaglinide vs. Glibenclamide (5 mg twice a day) was evaluated on Brachial reactivity parameters (p=<0.003). Repaglinide administration significantly improved brachial reactivity parameters (P<0.003) and reduced oxidative stress compared to glibenclamide in type 2 diabetic patients.
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