Matrix metalloproteinase-9 in an exploratory trial of intravenous minocycline for acute ischemic stroke - PubMed (original) (raw)
Clinical Trial
Matrix metalloproteinase-9 in an exploratory trial of intravenous minocycline for acute ischemic stroke
Jeffrey A Switzer et al. Stroke. 2011 Sep.
Abstract
Background and purpose: Plasma matrix metalloproteinase-9 levels predict posttissue plasminogen activator (tPA) hemorrhage.
Methods: 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.
Results: 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<0.0001; non-tPA, P=0.0019).
Conclusions: 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.
Figures
Figure 1
Levels of MMP-9 over time in MINOS. (A) MMP-9 levels in tPA-treated and tPA-untreated subjects at each timepoint in MINOS.Box = 25 to 75% interquartile range; horizontal line = median; vertical lines = range. *p < 0.0083. (B) A representative zymogram from a MINOS patient showing MMP-9 over time.
Figure 2
Levels of MMP-9 in MINOS and comparison subjects at 24 hours. MMP-9 in tPA-treated and tPA-untreated MINOS and comparison subjects at 24 hours. Box = 25 to 75% interquartile range; horizontal line = median; vertical lines = range. *p < 0.0125.
Comment in
- Letter by Lee regarding article, "Matrix metalloproteinase-9 in an exploratory trial of intravenous minocycline for acute stroke".
Lee R. Lee R. Stroke. 2011 Oct;42(10):e566; author reply e567. doi: 10.1161/STROKEAHA.111.632869. Epub 2011 Sep 8. Stroke. 2011. PMID: 21903959 No abstract available.
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