Clinical Comparison of Antiischemic Efficacy of Isosorbide Dinitrate and Molsidomine

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 randomi...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1998-01, Vol.31 (1), p.25-30
Hauptverfasser: Lehmann, Günter, Reiniger, Günther, Beyerle, Andrea, Schömig, Albert
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container_title Journal of cardiovascular pharmacology
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creator Lehmann, Günter
Reiniger, Günther
Beyerle, Andrea
Schömig, Albert
description 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.
doi_str_mv 10.1097/00005344-199801000-00004
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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 &lt; 0.001; at 8 h, −64%; p &lt; 0.01) than with molsidomine (2 h, −68%; p &lt; 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 &lt; 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.</description><subject>Antianginal agents. Coronary vasodilator agents</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiovascular system</subject><subject>Coronary Disease - complications</subject><subject>Coronary Disease - drug therapy</subject><subject>Cross-Over Studies</subject><subject>Delayed-Action Preparations - therapeutic use</subject><subject>Double-Blind Method</subject><subject>Exercise Test</subject><subject>Heart - drug effects</subject><subject>Heart - physiology</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Isosorbide Dinitrate - adverse effects</subject><subject>Isosorbide Dinitrate - blood</subject><subject>Isosorbide Dinitrate - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Molsidomine - adverse effects</subject><subject>Molsidomine - blood</subject><subject>Molsidomine - therapeutic use</subject><subject>Myocardial Ischemia - blood</subject><subject>Myocardial Ischemia - drug therapy</subject><subject>Myocardial Ischemia - etiology</subject><subject>Pharmacology. 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Coronary vasodilator agents</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiovascular system</topic><topic>Coronary Disease - complications</topic><topic>Coronary Disease - drug therapy</topic><topic>Cross-Over Studies</topic><topic>Delayed-Action Preparations - therapeutic use</topic><topic>Double-Blind Method</topic><topic>Exercise Test</topic><topic>Heart - drug effects</topic><topic>Heart - physiology</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Isosorbide Dinitrate - adverse effects</topic><topic>Isosorbide Dinitrate - blood</topic><topic>Isosorbide Dinitrate - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Molsidomine - adverse effects</topic><topic>Molsidomine - blood</topic><topic>Molsidomine - therapeutic use</topic><topic>Myocardial Ischemia - blood</topic><topic>Myocardial Ischemia - drug therapy</topic><topic>Myocardial Ischemia - etiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Vasodilator Agents - adverse effects</topic><topic>Vasodilator Agents - blood</topic><topic>Vasodilator Agents - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lehmann, Günter</creatorcontrib><creatorcontrib>Reiniger, Günther</creatorcontrib><creatorcontrib>Beyerle, Andrea</creatorcontrib><creatorcontrib>Schömig, Albert</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lehmann, Günter</au><au>Reiniger, Günther</au><au>Beyerle, Andrea</au><au>Schömig, Albert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Comparison of Antiischemic Efficacy of Isosorbide Dinitrate and Molsidomine</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>1998-01</date><risdate>1998</risdate><volume>31</volume><issue>1</issue><spage>25</spage><epage>30</epage><pages>25-30</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><coden>JCPCDT</coden><abstract>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 &lt; 0.001; at 8 h, −64%; p &lt; 0.01) than with molsidomine (2 h, −68%; p &lt; 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 &lt; 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.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9456273</pmid><doi>10.1097/00005344-199801000-00004</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Antianginal agents. Coronary vasodilator agents
Biological and medical sciences
Blood Pressure - drug effects
Cardiovascular system
Coronary Disease - complications
Coronary Disease - drug therapy
Cross-Over Studies
Delayed-Action Preparations - therapeutic use
Double-Blind Method
Exercise Test
Heart - drug effects
Heart - physiology
Heart Rate - drug effects
Humans
Isosorbide Dinitrate - adverse effects
Isosorbide Dinitrate - blood
Isosorbide Dinitrate - therapeutic use
Male
Medical sciences
Molsidomine - adverse effects
Molsidomine - blood
Molsidomine - therapeutic use
Myocardial Ischemia - blood
Myocardial Ischemia - drug therapy
Myocardial Ischemia - etiology
Pharmacology. Drug treatments
Vasodilator Agents - adverse effects
Vasodilator Agents - blood
Vasodilator Agents - therapeutic use
title Clinical Comparison of Antiischemic Efficacy of Isosorbide Dinitrate and Molsidomine
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