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基质金属蛋白酶-9 在静脉注射米诺环素治疗急性缺血性卒中的探索性试验中。

Matrix metalloproteinase-9 in an exploratory trial of intravenous minocycline for acute ischemic stroke.

机构信息

Department of Neurology, Medical College of Georgia, 1122 15th Street, Augusta, GA 30912, USA.

出版信息

Stroke. 2011 Sep;42(9):2633-5. doi: 10.1161/STROKEAHA.111.618215. Epub 2011 Jul 7.

DOI:10.1161/STROKEAHA.111.618215
PMID:21737808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3181080/
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.

摘要

背景与目的

血浆基质金属蛋白酶-9 水平可预测组织型纤溶酶原激活物(tPA)后出血。

方法

作者研究了米诺环素对 MINOS 试验和对照组急性缺血性脑卒中患者血浆基质金属蛋白酶-9 的影响。

结果

MINOS 组(tPA,P=0.0022;非 tPA,P=0.0066)与基线相比,72 小时时基质金属蛋白酶-9 水平较基线下降,且在 24 小时时低于非 MINOS 对照组(tPA,P<0.0001;非 tPA,P=0.0019)。

结论

MINOS 试验中接受 tPA 治疗的患者血浆基质金属蛋白酶-9 水平较低。米诺环素与 tPA 联合使用可能通过抑制基质金属蛋白酶-9 活性来预防溶栓治疗的不良后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620a/3181080/7668d46e8b31/nihms310871f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620a/3181080/5f201453900a/nihms310871f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620a/3181080/7668d46e8b31/nihms310871f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620a/3181080/5f201453900a/nihms310871f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620a/3181080/7668d46e8b31/nihms310871f2.jpg

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