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The effect of Ca2+ channel antagonists on plasma concentrations of matrix metalloproteinase-2 and -9 in essential hypertension
The ability of some antihypertensive drugs to protect from vascular damage in hypertension might be partially due to their ability to control matrix metalloproteinase (MMP)–mediated extracellular matrix metabolism, which in turn may contribute to vascular remodeling. This study was designed to inves...
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Published in: | American journal of hypertension 2004-03, Vol.17 (3), p.273-276 |
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container_title | American journal of hypertension |
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creator | Zervoudaki, Alexandra Economou, Emanuel Pitsavos, Christos Vasiliadou, Karmen Aggeli, Constantina Tsioufis, Konstantinos Toutouza, Marina Stefanadis, Christodoulos Toutouzas, Pavlos |
description | The ability of some antihypertensive drugs to protect from vascular damage in hypertension might be partially due to their ability to control matrix metalloproteinase (MMP)–mediated extracellular matrix metabolism, which in turn may contribute to vascular remodeling. This study was designed to investigate whether treatment with felodipine or diltiazem has any effect on plasma levels of MMP-2 and MMP-9 in essential hypertensive patients. We measured plasma levels of active MMP-2 and MMP-9 in 72 hypertensive subjects and 45 controls, both before and after 6 months of treatment with felodipine (group A) or diltiazem (group B). Mean adjusted differences, before and after each treatment, for MMP-2 and MMP-9 levels were: 19.8 (P = .01) for MMP-2, 0.2 (P = .5) for MMP-9 (group A), and 1.4 (P = .4) for MMP-2, 0.2 (P = .7) for MMP-9 (group B). These findings show that MMP-2 level is raised by treatment with felodipine but not diltiazem, whereas MMP-9 is unaffected by either treatment. |
doi_str_mv | 10.1016/j.amjhyper.2003.11.007 |
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This study was designed to investigate whether treatment with felodipine or diltiazem has any effect on plasma levels of MMP-2 and MMP-9 in essential hypertensive patients. We measured plasma levels of active MMP-2 and MMP-9 in 72 hypertensive subjects and 45 controls, both before and after 6 months of treatment with felodipine (group A) or diltiazem (group B). Mean adjusted differences, before and after each treatment, for MMP-2 and MMP-9 levels were: 19.8 (P = .01) for MMP-2, 0.2 (P = .5) for MMP-9 (group A), and 1.4 (P = .4) for MMP-2, 0.2 (P = .7) for MMP-9 (group B). These findings show that MMP-2 level is raised by treatment with felodipine but not diltiazem, whereas MMP-9 is unaffected by either treatment.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1941-7225</identifier><identifier>EISSN: 1879-1905</identifier><identifier>DOI: 10.1016/j.amjhyper.2003.11.007</identifier><identifier>PMID: 15001203</identifier><identifier>CODEN: AJHYE6</identifier><language>eng</language><publisher>New York, NY: Oxford University Press</publisher><subject>Adult ; Antihypertensive Agents - therapeutic use ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Biomarkers - blood ; Blood and lymphatic vessels ; Blood Pressure - drug effects ; Calcium Channel Blockers - therapeutic use ; Cardiology. Vascular system ; Diastole - drug effects ; Diltiazem - therapeutic use ; extracellular matrix ; Felodipine - therapeutic use ; Female ; Heart Ventricles - drug effects ; Humans ; Hypertension - blood ; Hypertension - enzymology ; Hypertension - physiopathology ; Male ; Matrix Metalloproteinase 2 - blood ; Matrix Metalloproteinase 2 - drug effects ; Matrix Metalloproteinase 9 - blood ; Matrix Metalloproteinase 9 - drug effects ; Medical sciences ; Metalloproteinases ; Middle Aged ; remodeling ; Systole - drug effects ; Treatment Outcome ; Vascular Resistance - drug effects</subject><ispartof>American journal of hypertension, 2004-03, Vol.17 (3), p.273-276</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Mar 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-217758696f8996be1be6d02d7077d0331aba866cc67eaf3f03ea1b7fda45a083</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15619787$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15001203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zervoudaki, Alexandra</creatorcontrib><creatorcontrib>Economou, Emanuel</creatorcontrib><creatorcontrib>Pitsavos, Christos</creatorcontrib><creatorcontrib>Vasiliadou, Karmen</creatorcontrib><creatorcontrib>Aggeli, Constantina</creatorcontrib><creatorcontrib>Tsioufis, Konstantinos</creatorcontrib><creatorcontrib>Toutouza, Marina</creatorcontrib><creatorcontrib>Stefanadis, Christodoulos</creatorcontrib><creatorcontrib>Toutouzas, Pavlos</creatorcontrib><title>The effect of Ca2+ channel antagonists on plasma concentrations of matrix metalloproteinase-2 and -9 in essential hypertension</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>The ability of some antihypertensive drugs to protect from vascular damage in hypertension might be partially due to their ability to control matrix metalloproteinase (MMP)–mediated extracellular matrix metabolism, which in turn may contribute to vascular remodeling. This study was designed to investigate whether treatment with felodipine or diltiazem has any effect on plasma levels of MMP-2 and MMP-9 in essential hypertensive patients. We measured plasma levels of active MMP-2 and MMP-9 in 72 hypertensive subjects and 45 controls, both before and after 6 months of treatment with felodipine (group A) or diltiazem (group B). Mean adjusted differences, before and after each treatment, for MMP-2 and MMP-9 levels were: 19.8 (P = .01) for MMP-2, 0.2 (P = .5) for MMP-9 (group A), and 1.4 (P = .4) for MMP-2, 0.2 (P = .7) for MMP-9 (group B). These findings show that MMP-2 level is raised by treatment with felodipine but not diltiazem, whereas MMP-9 is unaffected by either treatment.</description><subject>Adult</subject><subject>Antihypertensive Agents - therapeutic use</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure - drug effects</subject><subject>Calcium Channel Blockers - therapeutic use</subject><subject>Cardiology. Vascular system</subject><subject>Diastole - drug effects</subject><subject>Diltiazem - therapeutic use</subject><subject>extracellular matrix</subject><subject>Felodipine - therapeutic use</subject><subject>Female</subject><subject>Heart Ventricles - drug effects</subject><subject>Humans</subject><subject>Hypertension - blood</subject><subject>Hypertension - enzymology</subject><subject>Hypertension - physiopathology</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - blood</subject><subject>Matrix Metalloproteinase 2 - drug effects</subject><subject>Matrix Metalloproteinase 9 - blood</subject><subject>Matrix Metalloproteinase 9 - drug effects</subject><subject>Medical sciences</subject><subject>Metalloproteinases</subject><subject>Middle Aged</subject><subject>remodeling</subject><subject>Systole - drug effects</subject><subject>Treatment Outcome</subject><subject>Vascular Resistance - drug effects</subject><issn>0895-7061</issn><issn>1941-7225</issn><issn>1879-1905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpdkU2L1EAQhoMo7rj6F5YG0YskVqUn3clRBnWFHUQZULw0lU7FyZh0xu4e2L342-1xxg881aGe9-WFJ8uuEAoEVC93BU277d2efVECyAKxAND3sgU2S8x1WVb3swXUTZVrUHiRPQphBwBLpfBhdoEVAJYgF9mPzZYF9z3bKOZerKh8IeyWnONRkIv0dXZDiEHMTuxHChMJOzvLLnqKw-zCMTRR9MOtmDjSOM57P0ceHAXOy1TRibwRgxMcQkoNNIpfqyO7kPKPswc9jYGfnO9ltnnzerO6zm_ev323enWTW1nLmJeodVWrRvV106iWsWXVQdlp0LoDKZFaqpWyVmmmXvYgmbDVfUfLiqCWl9nzU20a9_3AIZppCJbHkRzPh2A0apBayQQ-_Q_czQfv0jSDUKpq2eimTJQ6UdbPIXjuzd4PE_m7BJmjHrMzv_WYox6DaJKeFLw61x_aibu_sbOPBDw7AxQsjb0nZ4fwD6ew0fWxKD9xSQ7f_vmT_2aUlroy15-_mI_rD1J-Wq8Nyp_S76tP</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Zervoudaki, Alexandra</creator><creator>Economou, Emanuel</creator><creator>Pitsavos, Christos</creator><creator>Vasiliadou, Karmen</creator><creator>Aggeli, Constantina</creator><creator>Tsioufis, Konstantinos</creator><creator>Toutouza, Marina</creator><creator>Stefanadis, Christodoulos</creator><creator>Toutouzas, Pavlos</creator><general>Oxford University Press</general><general>Elsevier Science</general><scope>BSCLL</scope><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><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20040301</creationdate><title>The effect of Ca2+ channel antagonists on plasma concentrations of matrix metalloproteinase-2 and -9 in essential hypertension</title><author>Zervoudaki, Alexandra ; Economou, Emanuel ; Pitsavos, Christos ; Vasiliadou, Karmen ; Aggeli, Constantina ; Tsioufis, Konstantinos ; Toutouza, Marina ; Stefanadis, Christodoulos ; Toutouzas, Pavlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-217758696f8996be1be6d02d7077d0331aba866cc67eaf3f03ea1b7fda45a083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Antihypertensive Agents - therapeutic use</topic><topic>Arterial hypertension. 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Vascular system</topic><topic>Diastole - drug effects</topic><topic>Diltiazem - therapeutic use</topic><topic>extracellular matrix</topic><topic>Felodipine - therapeutic use</topic><topic>Female</topic><topic>Heart Ventricles - drug effects</topic><topic>Humans</topic><topic>Hypertension - blood</topic><topic>Hypertension - enzymology</topic><topic>Hypertension - physiopathology</topic><topic>Male</topic><topic>Matrix Metalloproteinase 2 - blood</topic><topic>Matrix Metalloproteinase 2 - drug effects</topic><topic>Matrix Metalloproteinase 9 - blood</topic><topic>Matrix Metalloproteinase 9 - drug effects</topic><topic>Medical sciences</topic><topic>Metalloproteinases</topic><topic>Middle Aged</topic><topic>remodeling</topic><topic>Systole - drug effects</topic><topic>Treatment Outcome</topic><topic>Vascular Resistance - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zervoudaki, Alexandra</creatorcontrib><creatorcontrib>Economou, Emanuel</creatorcontrib><creatorcontrib>Pitsavos, Christos</creatorcontrib><creatorcontrib>Vasiliadou, Karmen</creatorcontrib><creatorcontrib>Aggeli, Constantina</creatorcontrib><creatorcontrib>Tsioufis, Konstantinos</creatorcontrib><creatorcontrib>Toutouza, Marina</creatorcontrib><creatorcontrib>Stefanadis, Christodoulos</creatorcontrib><creatorcontrib>Toutouzas, Pavlos</creatorcontrib><collection>Istex</collection><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><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zervoudaki, Alexandra</au><au>Economou, Emanuel</au><au>Pitsavos, Christos</au><au>Vasiliadou, Karmen</au><au>Aggeli, Constantina</au><au>Tsioufis, Konstantinos</au><au>Toutouza, Marina</au><au>Stefanadis, Christodoulos</au><au>Toutouzas, Pavlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of Ca2+ channel antagonists on plasma concentrations of matrix metalloproteinase-2 and -9 in essential hypertension</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>17</volume><issue>3</issue><spage>273</spage><epage>276</epage><pages>273-276</pages><issn>0895-7061</issn><eissn>1941-7225</eissn><eissn>1879-1905</eissn><coden>AJHYE6</coden><abstract>The ability of some antihypertensive drugs to protect from vascular damage in hypertension might be partially due to their ability to control matrix metalloproteinase (MMP)–mediated extracellular matrix metabolism, which in turn may contribute to vascular remodeling. This study was designed to investigate whether treatment with felodipine or diltiazem has any effect on plasma levels of MMP-2 and MMP-9 in essential hypertensive patients. We measured plasma levels of active MMP-2 and MMP-9 in 72 hypertensive subjects and 45 controls, both before and after 6 months of treatment with felodipine (group A) or diltiazem (group B). Mean adjusted differences, before and after each treatment, for MMP-2 and MMP-9 levels were: 19.8 (P = .01) for MMP-2, 0.2 (P = .5) for MMP-9 (group A), and 1.4 (P = .4) for MMP-2, 0.2 (P = .7) for MMP-9 (group B). These findings show that MMP-2 level is raised by treatment with felodipine but not diltiazem, whereas MMP-9 is unaffected by either treatment.</abstract><cop>New York, NY</cop><pub>Oxford University Press</pub><pmid>15001203</pmid><doi>10.1016/j.amjhyper.2003.11.007</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antihypertensive Agents - therapeutic use Arterial hypertension. Arterial hypotension Biological and medical sciences Biomarkers - blood Blood and lymphatic vessels Blood Pressure - drug effects Calcium Channel Blockers - therapeutic use Cardiology. Vascular system Diastole - drug effects Diltiazem - therapeutic use extracellular matrix Felodipine - therapeutic use Female Heart Ventricles - drug effects Humans Hypertension - blood Hypertension - enzymology Hypertension - physiopathology Male Matrix Metalloproteinase 2 - blood Matrix Metalloproteinase 2 - drug effects Matrix Metalloproteinase 9 - blood Matrix Metalloproteinase 9 - drug effects Medical sciences Metalloproteinases Middle Aged remodeling Systole - drug effects Treatment Outcome Vascular Resistance - drug effects |
title | The effect of Ca2+ channel antagonists on plasma concentrations of matrix metalloproteinase-2 and -9 in essential hypertension |
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