Effects of Edaravone, a Free Radical Scavenger, on Circulating Levels of MMP-9 and Hemorrhagic Transformation in Patients with Intravenous Thrombolysis Using Low-dose Alteplase

被引:20
作者
Tsuruoka, Atsushi [1 ]
Atsumi, Chihiro [1 ]
Mizukami, Heisuke [1 ]
Imai, Takeshi [1 ]
Hagiwara, Yuta [1 ]
Hasegawa, Yasuhiro [1 ]
机构
[1] St Marianna Univ, Sch Med, Dept Internal Med, Div Neurol, Kawasaki, Kanagawa 2168511, Japan
关键词
Tissue plasminogen activator; matrix metalloproteinase-9; hemorrhagic transformation; ACUTE ISCHEMIC-STROKE; TISSUE-PLASMINOGEN ACTIVATOR; TRANSIENT FOCAL ISCHEMIA; URIC-ACID; MATRIX-METALLOPROTEINASE; COMBINATION THERAPY; BRAIN-INJURY; MATRIX-METALLOPROTEINASE-9; MCI-186; COMPLICATIONS;
D O I
10.1016/j.jstrokecerebrovasdis.2014.07.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Matrix metalloproteinase-9 (MMP-9) plays a key role for the blood-brain barrier disruption and intravenous tissue plasminogen activator (iv-tPA) therapy increases MMP-9. Edaravone, a free radical scavenger, reduces MMP-9-related blood-brain barrier disruption. We aimed to investigate whether edaravone would suppress the MMP-9 increase after iv-tPA using low-dose alteplase (0.6 mg/kg). Subjects: Patients hospitalized within 12 hours after ischemic stroke onset between April 2008 and June 2013 were retrospectively examined. Patients with slight deficits (National Institutes of Health Stroke Scale score <= 4), stroke caused by arterial dissection, severe inflammatory disease or autoimmune disease, or regular use of steroid were excluded. Serum concentrations of high-sensitivity C-reactive protein, interleukin-6, MMP-2, and MMP-9 were serially measured at admission, after 24 hours, day 7, and day 14. General linear models were used to compare changes in concentrations of these biomarkers over time. Results: A total of 63 patients (38 men, aged 74.48 +/- 13.8 years) were studied. Patients were divided into 2 groups according to the iv-tPAtherapy, that is, tPAgroup (n = 32) and non-tPAgroup (n = 31). Edaravone was administered routinely except for contraindication (90.6% in the tPA group and 87.1% in the non-tPA group). Significant interaction of group x time factor was observed only in MMP-9 concentrations by repeated-measure analysis of variance (P = .004). Association between iv-tPAtherapy and subsequent hemorrhagic transformation was highly significant, but MMP-9 concentrations at any point did not predictive of subsequent hemorrhagic transformation (area under the receiver operating characteristic curve, .681). Conclusions: Low-dose iv-tPA increases MMP-9 concentration even in combination with Edaravone. The effect of higher dosage of Edaravone on circulating MMP-9 concentration and subsequent hemorrhagic transformation should be investigated.
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页码:2894 / 2899
页数:6
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