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High ICP as trigger of proinflammatory IL-6 cytokine activation in aneurysmal subarachnoid hemorrhage
被引:44
作者:
Graetz, Daniela
[1
]
Nagel, Alexandra
[1
]
Schlenk, Florian
[1
]
Sakowitz, Oliver
[2
]
Vajkoczy, Peter
[1
]
Sarrafzadeh, Asita
[1
]
机构:
[1] Charite, Dept Neurosurg, D-13353 Berlin, Germany
[2] Heidelberg Univ, Dept Neurosurg, Heidelberg, Germany
关键词:
Cerebral inflammation;
microdialysis;
intracranial hypertension;
subarachnoid hemorrhage;
interleukin-6;
CEREBROSPINAL-FLUID;
CEREBRAL MICRODIALYSIS;
INTERLEUKIN-6;
LEVELS;
BRAIN;
PERMEABILITY;
INFLAMMATION;
VASOSPASM;
DEFICITS;
D O I:
10.1179/016164109X12464612122650
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objective: There is a rising debate about the role of inflammation in the pathogenesis of complications after aneurysmal subarachnoid hemorrhage (SAH) such as intracranial hypertension (intracranial pressure, ICP>20 mmHg). This study aimed to analyse the origin of interleukin-6 (IL-6) in respect to ICP and cerebral metabolism in SAH patients. Methods: Prospectively, IL-6 was measured in three compartments, the extracellular fluid (ECF) monitored by cerebral microdialysis (MD), cerebrospinal fluid (CSF) and plasma for 10 days after SAH (days 0-4, three times daily; days 5-10, two times daily). Patients were classified having intracranial hypertension (n=7) or normal ICP (n=17) during 10 days after bleeding. Glasgow outcome scale (GOS) was assessed after 3 and 6 months. Results: Patient groups were comparable for age, WFNS and Fisher grade. Intracranial hypertension was associated with an inflammatory response, indicating activation of the inflammatory cascade in the brain (ECF) and systemic circulation with high IL-6 and C-reactive protein (CRP) plasma levels after SAH, the latter associated with unfavourable outcome. The data suggest the ECF but not the CSF as main origin of IL-6 in the systemic circulation in the presence of intracranial hypertension in SAH. Discussion: Intracranial hypertension is associated with a strong activation of the inflammatory cascade in the brain and systemic circulation, and might be underestimated as proinflammmatory trigger in the pathogenesis of complications after SAH. Future therapies targeting anti-inflammatory response in plasma may help to reduce the inflammatory cascade responsible for development of intracranial hypertension.
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页码:728 / 735
页数:8
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