The decrease in procarboxypeptidase U (TAFI) concentration in acute ischemic stroke correlates with stroke severity, evolution and outcome

被引:32
作者
Brouns, R. [2 ,3 ,4 ,5 ]
Heylen, E. [1 ]
Willemse, J. L. [1 ]
Sheorajpanday, R. [2 ,3 ,4 ]
De Surgeloose, D. [6 ]
Verkerk, R. [1 ]
De Deyn, P. P. [2 ,3 ,4 ]
Hendriks, D. F. [1 ]
机构
[1] Univ Antwerp, Med Biochem Lab, B-2020 Antwerp, Belgium
[2] ZNA Middelheim Hosp, Dept Neurol, Antwerp, Belgium
[3] ZNA Middelheim Hosp, Memory Clin, Antwerp, Belgium
[4] Univ Antwerp, Lab Neurochem & Behav, Inst Born Bunge, Dept Biomed Sci, B-2020 Antwerp, Belgium
[5] Vrije Univ Brussel, Univ Hosp Brussels, Dept Neurol, Brussels, Belgium
[6] ZNA Middelheim Hosp, Dept Radiol, Antwerp, Belgium
关键词
acute cerebral infarction; procarboxypeptidase U; stroke evolution; stroke outcome; stroke severity; TAFI; ACTIVATABLE FIBRINOLYSIS INHIBITOR; JUGULAR-VEIN THROMBOLYSIS; DOG-MODEL; IN-VIVO; CARBOXYPEPTIDASE; PLASMA; PHASE; RISK; INACTIVATION; THRESHOLD;
D O I
10.1111/j.1538-7836.2009.03663.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: Procarboxypeptidase U (proCPU, TAFI) concentration in plasma is potentially related to thrombotic tendency, and elevated proCPU levels have been reported in ischemic stroke patients. Improved insight into the role of proCPU in acute ischemic stroke is essential for the development of more adequate therapeutics that may include carboxypeptidase inhibitors. In this study we investigated whether the plasma concentration of proCPU and the proCPU kinetic profile in acute ischemic stroke are related to initial stroke severity, stroke evolution in the subacute phase and long-term stroke outcome. Methods: Plasma concentration of proCPU was assessed in 136 stroke patients at admission (7.5 h after stroke onset), at 24 h, at 72 h and at day 7 after stroke onset. We evaluated the relation between change in proCPU concentrations and (a) stroke severity (patients with TIA vs. stroke patients, NIHSS score at admission), (b) stroke evolution (stroke progression, infarct volume at 72 h), and (c) stroke outcome (mRS score at month 3). Results: ProCPU concentration decreased significantly in the first 72 h after stroke onset and thereafter returned to baseline. This biphasic time course, with its nadir at 72 h, was more pronounced in patients with severe stroke, unfavourable stroke evolution in the first 72 h and poor long-term outcome. Conclusions: The decrease in proCPU concentration in the first 72 h after stroke onset correlates with more severe stroke, unfavourable stroke evolution, and poor long-term stroke outcome.
引用
收藏
页码:75 / 80
页数:6
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