Brain interstitial fluid TNF-alpha after subarachnoid hemorrhage.
Brain interstitial fluid TNF-alpha after subarachnoid hemorrhage.
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DOI:
10.1016/j.jns.2009.12.023
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发表时间:
2010-04-15
影响因子:
4.4
通讯作者:
Badjatia, Neeraj
中科院分区:
文献类型:
--
作者:
Hanafy, Khalid A.;Grobelny, Bartosz;Fernandez, Luis;Kurtz, Pedro;Connolly, E. S.;Mayer, Stephan A.;Schindler, Christian;Badjatia, Neeraj
关键词:
TNF-α is an inflammatory cytokine that plays a central role in promoting the cascade of events leading to an inflammatory response. Recent studies have suggested that TNF-α may play a key role in the formation and rupture of cerebral aneurysms, and that the underlying cerebral inflammatory response is a major determinate of outcome following subrarachnoid hemorrhage (SAH). We studied 14 comatose SAH patients who underwent multimodality neuromonitoring with intracranial pressure (ICP) and cerebral microdialysis as part of their clinical care. Continuous physiological variables were time-locked every 8 hours and recorded at the same point that brain interstitial fluid TNF-α was measured in brain microdialysis samples. Significant associations were determined using generalized estimation equations. Each patient had a mean of 9 brain tissue TNF-α measurements obtained over an average of 72 hours of monitoring. TNF-α levels rose progressively over time. Predictors of elevated brain interstitial TNF-α included higher brain interstitial fluid glucose levels (β=0.066, P<0.02), intraventricular hemorrhage (β=0.085, P<0.021), and aneurysm size >6 mm (β=0.14, p<0.001). There was no relationship between TNF-α levels and the burden of cisternal SAH; concurrent measurements of serum glucose, or lactate-pyruvate ratio. Brain interstitial TNF-α levels are elevated after SAH, and are associated with large aneurysm size, the burden of intraventricular blood, and elevation brain interstitial glucose levels.
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影响因子:
3.5
作者:
Hui, Ferdinand K.;Tumialan, Luis M.;Zhang, Y. Jonathan
通讯作者:
Zhang, Y. Jonathan
影响因子:
2
作者:
Kang, Dong-Hun;Park, Jaechan;Hamm, In-Suk
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Hamm, In-Suk
影响因子:
8.3
作者:
HIJDRA, A;VANGIJN, J;VANCREVEL, H
通讯作者:
VANCREVEL, H
影响因子:
8.8
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Claassen, J;Vu, A;Mayer, SA
通讯作者:
Mayer, SA
影响因子:
8.3
作者:
Claassen, J;Carhuapoma, JR;Mayer, SA
通讯作者:
Mayer, SA