Matrix Metalloproteinase-9 and Recovery of Acute Ischemic Stroke

被引:30
作者
Abdelnaseer, Maged M. [1 ]
Elfauomy, Nervana M. [1 ]
Esmail, Eman H. [1 ]
Kamal, Manal M. [2 ]
Elsawy, Enji H. [1 ]
机构
[1] Cairo Univ, Dept Neurol, Giza, Egypt
[2] Cairo Univ, Clin & Chem Pathol Dept, Giza, Egypt
关键词
Matrix metalloproteinase; stroke; outcome; predictor; recovery; NIHSS; modified Rankin Scale; FOCAL CEREBRAL-ISCHEMIA; BLOOD-BRAIN-BARRIER; MATRIX METALLOPROTEINASES; NEURONAL DAMAGE; GELATINASE-B; URIC-ACID; INHIBITOR; REPERFUSION; DISRUPTION; EXPRESSION;
D O I
10.1016/j.jstrokecerebrovasdis.2016.09.043
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Background: Stroke outcome can be predicted by clinical features, biochemical parameters, and some risk factors. Matrix metalloproteinase-9 (MMP-9) is involved in various stages of stroke pathology. MMP-9 inhibitors are potential stroke therapeutic agents. Little is known about the relation between MMP-9-after the acute stage- and clinical recovery. Objective: The study aimed to investigate the serum level of MMP-9 at stroke onset as predictor of stroke outcome and the relation between the level of MMP-9 after 30 days and stroke recovery. Methods: The National Institutes of Health Stroke Scale, modified Rankin Scale, and serum level of MMP-9 were assessed in 30 patients with acute ischemic stroke during the first 24 hours of onset and then a month later. None of the patients received thrombolytic therapy. Thirty normal volunteers of matched age and sex were included in the control group. Results: The serum level of MMP-9 at stroke onset was independently positively correlated with stroke outcome. The serum level of MMP-9 30 days after stroke onset was positively correlated with initial stroke severity and outcome, as well as with clinical recovery. Conclusion: Higher serum level of MMP-9 at stroke onset can be a predictor of poor stroke outcome. However, beyond the acute stage, MMP-9 may play beneficial role in stroke recovery. (C) 2017 National Stroke Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:733 / 740
页数:8
相关论文
共 58 条
[1]
Serum matrix metalloproteinase-9 in acute ischemic stroke and its relation to stroke severity [J].
Abdelnaseer, Maged ;
Elfayomi, Nervana ;
Hassan, Eman ;
Kamal, Manal ;
Hamdy, Ahmed ;
Elsawy, Enji .
EGYPTIAN JOURNAL OF NEUROLOGY PSYCHIATRY AND NEUROSURGERY, 2015, 52 (04) :274-278
[2]
Relationship between matrix metalloproteinase-9 and common carotid artery intima media thickness [J].
Abdelnaseer, Maged ;
Elfayomi, Nervana ;
Esmail, Eman H. ;
Kamal, Manal M. ;
Hamdy, Ahmed ;
Samie, Rasha M. Abdel ;
Elsawy, Enji .
NEUROLOGICAL SCIENCES, 2016, 37 (01) :117-122
[3]
AHO K, 1980, B WORLD HEALTH ORGAN, V58, P113
[4]
Course of matrix metalloproteinase-9 isoforms after the administration of uric acid in patients with acute stroke A proof-of-concept study [J].
Amaro, Sergio ;
Obach, Victor ;
Cervera, Alvaro ;
Urra, Xabier ;
Gomez-Choco, Manuel ;
Planas, Anna M. ;
Chamorro, Angel .
JOURNAL OF NEUROLOGY, 2009, 256 (04) :651-656
[5]
Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732
[6]
HMG-CoA reductase inhibitors reduce MMP-9 secretion by macrophages [J].
Bellosta, S ;
Via, D ;
Canavesi, M ;
Pfister, P ;
Fumagalli, R ;
Paoletti, R ;
Bernini, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (11) :1671-1678
[7]
Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[8]
Percent Change on the National Institutes of Health Stroke Scale: A Useful Acute Stroke Outcome Measure [J].
Bruno, Askiel ;
Saha, Chandan ;
Williams, Linda S. .
JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2009, 18 (01) :56-59
[9]
Doxycycline inhibits MMPs via modulation of plasminogen activators in focal cerebral ischemia [J].
Burggraf, Dorothe ;
Trinkl, Andreas ;
Dichgans, Martin ;
Hamann, Gerhard F. .
NEUROBIOLOGY OF DISEASE, 2007, 25 (03) :506-513
[10]
Cyclooxygenase inhibition limits blood-brain barrier disruption following intracerebral injection of tumor necrosis factor-α in the rat [J].
Candelario-Jalil, Eduardo ;
Taheri, Saeid ;
Yang, Yi ;
Sood, Rohit ;
Grossetete, Mark ;
Estrada, Eduardo Y. ;
Fiebich, Bernd L. ;
Rosenberg, Gary A. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 323 (02) :488-498