Key result
Repaglinide eliminates myocardial ischemic preconditioning in ~83% of patients with coronary disease and diabetes.
Why the study?
ATP-sensitive K(+) channel blockers such as glinides may induce loss of ischemic preconditioning in patients with diabetes and coronary artery disease.
Does repaglinide reduce ischemic preconditioning in patients with type 2 diabetes and stable angina pectoris?
Does repaglinide reduce ischemic preconditioning in patients with type 2 diabetes and stable angina pectoris?
Repaglinide eliminates myocardial ischemic preconditioning in patients with type 2 diabetes and coronary artery disease, which may have implications for its cardiovascular safety profile during ischemic events.
Repaglinide abolished ischemic preconditioning in 83% of diabetic multivessel CAD patients; larger trials needed before changing therapy.
OBJECTIVE: Ischemic preconditioning is an increased tolerance to myocardial ischemia during the second of two consecutive exercise tests. ATP-sensitive K(+) channel blockers, such as glinides and sulfonylurea drugs, can induce loss of ischemic preconditioning. This study aimed to investigate the effects of repaglinide, a hypoglycemic agent with an affinity for myocardial ATP-sensitive K (+)channels, on the results of consecutive exercise tests in patients with diabetes and multivessel coronary artery disease. METHODS: Forty-two patients with type 2 diabetes and chronic stable angina pectoris, and two-vessel or three-vessel disease participated in this study. The patients underwent two consecutive treadmill exercise tests (phase 1). On the day after these exercise tests, 2 mg of oral repaglinide was given to the patients. One week later, two exercise tests were repeated consecutively (phase 2). RESULTS: All patients achieved 1.0-mm ST-segment depression during the four exercise tests (T1, T2, T3, and T4). In phase 2, seven patients improved in time to onset of 1.0-mm ST-segment depression. The worsening of the time to onset of 1.0-mm ST-segment depression in phase 2 demonstrated ischemic preconditioning block in 83.3% of patients (P=0.0001). Even the postexercise electrocardiographic parameters (ST-segment depression morphology and magnitude and arrhythmias) were significantly different between the groups with and without pharmacologic ischemic preconditioning block (P=0.031). CONCLUSIONS: Repaglinide, an oral hypoglycemic agent with ATP-sensitive K(+) channel-blocker activity, eliminated the myocardial ischemic preconditioning in patients with coronary disease and diabetes.
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Hueb et al. (2006) studied Type 2 diabetes and chronic stable angina pectoris with multivessel coronary artery disease (n=42). Repaglinide vs. Baseline (phase 1 without repaglinide) was evaluated on Ischemic preconditioning block (worsening of the time to onset of 1.0-mm ST-segment depression) (p=0.0001). Repaglinide eliminated myocardial ischemic preconditioning, causing ischemic preconditioning block in 83.3% of patients with coronary disease and diabetes (P=0.0001).
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