Transient ischemic attacks before ischemic stroke:: Preconditioning the human brain?: A multicenter magnetic resonance imaging study

被引:238
作者
Wegener, S
Gottschalk, B
Jovanovic, V
Knab, R
Fiebach, JB
Schellinger, PD
Kucinski, T
Jungehülsing, GJ
Brunecker, P
Müller, B
Banasik, A
Amberger, N
Wernecke, KD
Siebler, M
Röther, J
Villringer, A
Weih, M
机构
[1] Univ Hosp Charite, Dept Neurol, D-10117 Berlin, Germany
[2] Univ Dusseldorf, Dept Neurol, D-4000 Dusseldorf, Germany
[3] Univ Hamburg, Dept Neurol, Eppendorf, Germany
[4] Univ Hamburg, Dept Neuroradiol, Eppendorf, Germany
[5] Univ Heidelberg, Dept Neuroradiol, Heidelberg, Germany
[6] Univ Heidelberg, Dept Neurol, Heidelberg, Germany
[7] Humboldt Univ, Inst Med Biometr, Berlin, Germany
[8] Univ Freiburg, Fac Med, Freiburg, Germany
关键词
ischemic attack; transient; ischemic preconditioning; magnetic resonance imaging; neuroprotection; stroke;
D O I
10.1161/01.STR.0000115767.17923.6A
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - We investigated whether transient ischemic attacks ( TIAs) before stroke can induce tolerance by raising the threshold of tissue vulnerability in the human brain. Methods - Sixty-five patients with first-ever ischemic territorial stroke received diffusion- and perfusion-weighted MRI within 12 hours of symptom onset. Epidemiological and clinical data, lesion volumes in T2, apparent diffusion coefficient ( ADC) maps and perfusion maps, and cerebral blood flow and cerebral blood volume values were compared between patients with and without a prodromal TIA. Results - Despite similar size and severity of the perfusion deficit, initial diffusion lesions tended to be smaller and final infarct volumes were significantly reduced ( final T2: 9.1 [interquartile range, 19.7] versus 36.5 [91.2] mL; P = 0.014) in patients with a history of TIA ( n = 16). This was associated with milder clinical deficits. Conclusions - The beneficial effect of TIAs on lesion size in ADC and T2 suggests the existence of endogenous neuroprotection in the human brain.
引用
收藏
页码:616 / 621
页数:6
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