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 |
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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 < 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.</description><identifier>ISSN: 0160-2446</identifier><identifier>EISSN: 1533-4023</identifier><identifier>DOI: 10.1097/00005344-199801000-00004</identifier><identifier>PMID: 9456273</identifier><identifier>CODEN: JCPCDT</identifier><language>eng</language><publisher>Philadelphia, PA: Lippincott-Raven Publishers</publisher><subject>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</subject><ispartof>Journal of cardiovascular pharmacology, 1998-01, Vol.31 (1), p.25-30</ispartof><rights>Lippincott-Raven Publishers</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4344-6e0133688c73b53363e4cd0049ce35bbd60edc0a5be674b44a95c4268b98967d3</citedby><cites>FETCH-LOGICAL-c4344-6e0133688c73b53363e4cd0049ce35bbd60edc0a5be674b44a95c4268b98967d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00005344-199801000-00004$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>314,776,780,4010,4595,27900,27901,27902,65206</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2117444$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9456273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lehmann, Günter</creatorcontrib><creatorcontrib>Reiniger, Günther</creatorcontrib><creatorcontrib>Beyerle, Andrea</creatorcontrib><creatorcontrib>Schömig, Albert</creatorcontrib><title>Clinical Comparison of Antiischemic Efficacy of Isosorbide Dinitrate and Molsidomine</title><title>Journal of cardiovascular pharmacology</title><addtitle>J Cardiovasc Pharmacol</addtitle><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.</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. Drug treatments</subject><subject>Vasodilator Agents - adverse effects</subject><subject>Vasodilator Agents - blood</subject><subject>Vasodilator Agents - therapeutic use</subject><issn>0160-2446</issn><issn>1533-4023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1OwzAQhC0EKqXwCEg5cA3Y8caJj1UoUKmISzlH_otqSOLKTlX17XFo6Q1fLO_MrHY_I5QQ_EgwL55wPDkFSAnnJSbxlY4luEBTklOaAs7oJZpiwnCaAbBrdBPCF8YE8oJN0IRDzrKCTtG6am1vlWiTynVb4W1wfeKaZN4P1ga1MZ1VyaJpokUdRmEZXHBeWm2S55gcvBhMInqdvLs2WO0625tbdNWINpi70z1Dny-LdfWWrj5el9V8lSoYZ2cGE0pZWaqCyjg1owaUjltwZWgupWbYaIVFLg0rQAIInivIWCl5yVmh6QyVx77KuxC8aeqtt53wh5rgeuRU_3Gqz5x-SxCj98fodic7o8_BE5ioP5x0ESKdxote2XC2ZYQUAGMbONr2rh2MD9_tbm98vTGiHTb1f79EfwAEmn72</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Lehmann, Günter</creator><creator>Reiniger, Günther</creator><creator>Beyerle, Andrea</creator><creator>Schömig, Albert</creator><general>Lippincott-Raven Publishers</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199801</creationdate><title>Clinical Comparison of Antiischemic Efficacy of Isosorbide Dinitrate and Molsidomine</title><author>Lehmann, Günter ; Reiniger, Günther ; Beyerle, Andrea ; Schömig, Albert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4344-6e0133688c73b53363e4cd0049ce35bbd60edc0a5be674b44a95c4268b98967d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Antianginal agents. 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 < 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.</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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source | Ovid Lippincott Williams and Wilkins Journal Legacy Archive; MEDLINE; EZB Electronic Journals Library; Journals@Ovid Complete |
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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