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血清中S100B、S100A1B和S100BB的水平均与重度创伤性脑损伤后的预后相关。

Serum levels of S100B, S100A1B and S100BB are all related to outcome after severe traumatic brain injury.

作者信息

Nylén K, Ost M, Csajbok L Z, Nilsson I, Hall C, Blennow K, Nellgård B, Rosengren L

机构信息

Department of Neurology, Institute of Clinical Neuroscience, Sahlgrenska University Hospital, University of Göteborg, Göteborg, Sweden.

出版信息

Acta Neurochir (Wien). 2008 Mar;150(3):221-7; discussion 227. doi: 10.1007/s00701-007-1489-2. Epub 2008 Jan 14.

Abstract

OBJECTIVES

S100B is an established marker of brain damage. Used in the context as a biochemical marker, S100B denotes a measurement of all S100 proteins, including at least one S100B monomer, i.e. the sum of the two dimers S100A1B and S100BB. Almost all published studies are based on this "sum concentration". However, the brain specificity of S100B has been questioned and increased serum levels have also been reported after trauma without head injury. Since the S100B monomer dominates in the brain, we hypothesised that the S100BB dimer should be better related to outcome after severe traumatic brain injury than S100A1B or the "sum concentration".

METHODS

Daily serum samples were collected from 59 patients with severe traumatic brain injury. Three different ELISA methods were used for measurements of S100B, S100A1B and S100BB respectively. Outcome was assessed after one year and categorised according to the Glasgow Outcome Scale.

RESULTS

Serum levels of S100B, S100A1B and S100BB followed the same temporal course, with early maximum and rapidly decreasing values over the first days after the trauma. Maximum serum concentrations of each of the parameters were increased in the patient group with an unfavourable outcome compared with those with a favourable outcome (p = 0.01, 0.006 and 0.004, respectively).

CONCLUSION

Both S100A1B and S100BB were related to outcome after severe traumatic brain injury. Even though this study is small, it seems unlikely that separate analyses of the dimers are of any advantage compared with measuring S100B alone.

摘要

目的

S100B是一种公认的脑损伤标志物。在作为生化标志物的背景下,S100B表示对所有S100蛋白的测量,包括至少一个S100B单体,即两个二聚体S100A1B和S100BB的总和。几乎所有已发表的研究都是基于这种“总和浓度”。然而,S100B的脑特异性受到质疑,并且在无头部损伤的创伤后也有血清水平升高的报道。由于S100B单体在脑中占主导地位,我们推测与严重创伤性脑损伤后的预后相比,S100BB二聚体应比S100A1B或“总和浓度”更相关。

方法

从59例严重创伤性脑损伤患者中每日采集血清样本。分别使用三种不同的酶联免疫吸附测定(ELISA)方法测量S100B、S100A1B和S100BB。一年后评估预后,并根据格拉斯哥预后量表进行分类。

结果

S100B、S100A1B和S100BB的血清水平遵循相同的时间进程,在创伤后的头几天内早期达到最大值并迅速下降。与预后良好的患者组相比,预后不良的患者组中每个参数的最大血清浓度均升高(分别为p = 0.01、0.006和0.004)。

结论

S100A1B和S100BB均与严重创伤性脑损伤后的预后相关。尽管这项研究规模较小,但与单独测量S100B相比,对二聚体进行单独分析似乎没有任何优势。

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