Why the study?
Does sustained-release isosorbide dinitrate compared to molsidomine improve acute antiischemic effects in patients with coronary artery disease?
Does sustained-release isosorbide dinitrate compared to molsidomine improve acute antiischemic effects in patients with coronary artery disease?
Isosorbide dinitrate provides stronger antiischemic effects up to 8 hours compared to molsidomine, but neither drug achieves full 24-hour coverage due to early tolerance or short half-life.
Isosorbide dinitrate may be preferred for acute antiischemic effects in CAD; reinforces limits of sustained-release nitrates for 24-hour coverage.
In 16 patients with documented coronary artery disease, the extent and duration of acute antiischemic and hemodynamic effects of monotherapies with 120 mg of sustained-release isosorbide dinitrate once daily and 8 mg of sustained-release molsidomine 3 times daily were compared according to a randomized, double-blind, cross-over and placebo-controlled protocol including exercise testing for assessment of ST-segment depression (ST) at an identical workload and determination of plasma concentrations of both substances. Up to 8 h after dosing in the morning, more marked and sustained effects were observed with the nitrate (ST at 2 h, -82%; p < 0.001; at 8 h, -64%; p < 0.01) than with molsidomine (2 h, -68%; p < 0.001; at 8 h, -9%; NS). At 12 h, no more meaningful actions were detectable with isosorbide dinitrate (-13%, NS) despite plasma concentrations still within a range otherwise considered therapeutically effective, whereas with molsidomine, at 4 h after renewed dosing, this parameter was reduced by 38% (p < 0.01). However, therapeutic coverage over a 24-h period could be demonstrated on neither regimen, in the case of the nitrate because of the development of early tolerance, and in the case of molsidomine with its meaningfully shorter half-life because of the necessity of increasing the dosing frequency even further. No meaningful adverse effects were observed with either regimen. Nonresponders, overall a minority on one treatment, responded completely to the alternative regimen and vice versa.
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Lehmann et al. (1998) studied this question.
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