Matrix Metalloproteinase-9 in an Exploratory Trial of Intravenous Minocycline for Acute Ischemic Stroke

Plasma matrix metalloproteinase-9 levels predict posttissue plasminogen activator (tPA) hemorrhage. The authors investigated the effect of minocycline on plasma matrix metalloproteinase-9 in acute ischemic stroke in the Minocycline to Improve Neurological Outcome in Stroke (MINOS) trial and a compar...

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Veröffentlicht in:Stroke (1970) 2011-09, Vol.42 (9), p.2633-2635
Hauptverfasser: SWITZER, Jeffrey A, HESS, David C, ERGUL, Adviye, WALLER, Jennifer L, MACHADO, Livia S, PORTIK-DOBOS, Vera, CREED PETTIGREW, L, CLARK, Wayne M, FAGAN, Susan C
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container_end_page 2635
container_issue 9
container_start_page 2633
container_title Stroke (1970)
container_volume 42
creator SWITZER, Jeffrey A
HESS, David C
ERGUL, Adviye
WALLER, Jennifer L
MACHADO, Livia S
PORTIK-DOBOS, Vera
CREED PETTIGREW, L
CLARK, Wayne M
FAGAN, Susan C
description Plasma matrix metalloproteinase-9 levels predict posttissue plasminogen activator (tPA) hemorrhage. The authors investigated the effect of minocycline on plasma matrix metalloproteinase-9 in acute ischemic stroke in the Minocycline to Improve Neurological Outcome in Stroke (MINOS) trial and a comparison group. Matrix metalloproteinase-9 level decreased at 72 hours compared with baseline in MINOS (tPA, P=0.0022; non-tPA, P=0.0066) and was lower than in the non-MINOS comparison group at 24 hours (tPA, P
doi_str_mv 10.1161/STROKEAHA.111.618215
format Article
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The authors investigated the effect of minocycline on plasma matrix metalloproteinase-9 in acute ischemic stroke in the Minocycline to Improve Neurological Outcome in Stroke (MINOS) trial and a comparison group. Matrix metalloproteinase-9 level decreased at 72 hours compared with baseline in MINOS (tPA, P=0.0022; non-tPA, P=0.0066) and was lower than in the non-MINOS comparison group at 24 hours (tPA, P&lt;0.0001; non-tPA, P=0.0019). Lower plasma matrix metalloproteinase-9 was seen among tPA-treated subjects in the MINOS trial. Combining minocycline with tPA may prevent the adverse consequences of thrombolytic therapy through suppression of matrix metalloproteinase-9 activity.</description><subject>Aged</subject><subject>Anti-Bacterial Agents - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Brain Ischemia - blood</subject><subject>Brain Ischemia - drug therapy</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Matrix Metalloproteinase 9 - blood</subject><subject>Matrix Metalloproteinase Inhibitors</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Minocycline - administration &amp; dosage</subject><subject>Neurology</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Stroke - blood</topic><topic>Stroke - drug therapy</topic><topic>Thrombolytic Therapy - methods</topic><topic>Tissue Plasminogen Activator - administration &amp; dosage</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SWITZER, Jeffrey A</creatorcontrib><creatorcontrib>HESS, David C</creatorcontrib><creatorcontrib>ERGUL, Adviye</creatorcontrib><creatorcontrib>WALLER, Jennifer L</creatorcontrib><creatorcontrib>MACHADO, Livia S</creatorcontrib><creatorcontrib>PORTIK-DOBOS, Vera</creatorcontrib><creatorcontrib>CREED PETTIGREW, L</creatorcontrib><creatorcontrib>CLARK, Wayne M</creatorcontrib><creatorcontrib>FAGAN, Susan C</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><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SWITZER, Jeffrey A</au><au>HESS, David C</au><au>ERGUL, Adviye</au><au>WALLER, Jennifer L</au><au>MACHADO, Livia S</au><au>PORTIK-DOBOS, Vera</au><au>CREED PETTIGREW, L</au><au>CLARK, Wayne M</au><au>FAGAN, Susan C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Matrix Metalloproteinase-9 in an Exploratory Trial of Intravenous Minocycline for Acute Ischemic Stroke</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>42</volume><issue>9</issue><spage>2633</spage><epage>2635</epage><pages>2633-2635</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>Plasma matrix metalloproteinase-9 levels predict posttissue plasminogen activator (tPA) hemorrhage. 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source MEDLINE; American Heart Association Journals; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Aged
Anti-Bacterial Agents - administration & dosage
Biological and medical sciences
Blood. Blood coagulation. Reticuloendothelial system
Brain Ischemia - blood
Brain Ischemia - drug therapy
Female
Fibrinolytic Agents - administration & dosage
Humans
Infusions, Intravenous
Male
Matrix Metalloproteinase 9 - blood
Matrix Metalloproteinase Inhibitors
Medical sciences
Middle Aged
Minocycline - administration & dosage
Neurology
Pharmacology. Drug treatments
Stroke - blood
Stroke - drug therapy
Thrombolytic Therapy - methods
Tissue Plasminogen Activator - administration & dosage
Vascular diseases and vascular malformations of the nervous system
title Matrix Metalloproteinase-9 in an Exploratory Trial of Intravenous Minocycline for Acute Ischemic Stroke
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