McKeating E G, Andrews P J, Mascia L
Department of Anaesthetics, University of Edinburgh, Western General Hospital, U.K.
Acta Neurochir Suppl. 1998;71:200-2. doi: 10.1007/978-3-7091-6475-4_57.
Adhesion molecules have an important role in leukocyte migration into tissue after injury. We hypothesised that changes in ICAM-1 and L-selectin expression after traumatic brain injury would result in altered serum concentrations of these molecules, which would be related to injury severity and outcome. We investigated arterial and jugular venous concentrations of ICAM-1 and L-selectin in 22 patients. The Glasgow Coma Score and Injury Severity Score were recorded. Paired arterial and jugular venous blood samples were taken at designated times after brain injury: on admission, at 24 hours, 48 hours and 96 hours. Glasgow Outcome Scores at 6 months were obtained. Mean serum concentrations of ICAM-1 were normal on admission, but became significantly increased by 96 hours (p = 0.018). Mean L-selectin concentrations wre markedly below controls at all time points (p < 0.001). There were no significant differences between jugular venous and arterial concentrations of either ICAM-1 or L-selectin. Serum ICAM-1 was significantly related to neurological outcome (p < 0.001) and to the Glasgow Coma Score (p < 0.001). These changes in adhesion molecules expression may be important in the pathophysiology of secondary injury. The highly significant relationship between serum ICAM-1 and neurological outcome suggests that drugs which antagonize adhesion molecule activity may improve outcome after traumatic brain injury.
黏附分子在损伤后白细胞向组织内迁移过程中起重要作用。我们推测,创伤性脑损伤后细胞间黏附分子-1(ICAM-1)和淋巴细胞功能相关抗原-1(L-选择素)表达的变化会导致这些分子血清浓度的改变,而这与损伤严重程度和预后相关。我们调查了22例患者动脉血和颈静脉血中ICAM-1和L-选择素的浓度。记录格拉斯哥昏迷评分和损伤严重程度评分。在脑损伤后的指定时间采集配对的动脉血和颈静脉血样本:入院时、24小时、48小时和96小时。获取6个月时的格拉斯哥预后评分。入院时ICAM-1的平均血清浓度正常,但到96小时时显著升高(p = 0.018)。所有时间点L-选择素的平均浓度均明显低于对照组(p < 0.001)。ICAM-1和L-选择素的颈静脉血浓度与动脉血浓度之间均无显著差异。血清ICAM-1与神经功能预后显著相关(p < 0.001),与格拉斯哥昏迷评分也显著相关(p < 0.001)。黏附分子表达的这些变化可能在继发性损伤的病理生理学中起重要作用。血清ICAM-1与神经功能预后之间的高度显著关系表明,拮抗黏附分子活性的药物可能会改善创伤性脑损伤后的预后。