Stroick Mark, Fatar Marc, Ragoschke-Schumm Andreas, Fassbender Klaus, Bertsch Thomas, Hennerici Michael G
Department of Neurology, Universitätsklinikum Mannheim, University of Heidelberg, Germany.
Curr Med Chem. 2006;13(25):3053-60. doi: 10.2174/092986706778521751.
The assessment of S-100B in acute neurological disorders such as global hypoxia, ischaemic or haemorrhagic stroke and traumatic brain injury reflects severity of symptoms and outcome. However, the temporal profile of S-100B release depends on topography, intensity and pathophysiology of the damage e.g. immediate release after traumatic brain injury following the acute destruction of neuronal tissue or delayed release after ischaemic stroke in which gradual breakdown of the blood-brain barrier plays a crucial role. In chronic brain diseases, knowledge about the clinical value of quantification of S-100B is scarce and further evaluations are needed. This review considers both conditions for S-100B measurement and illustrates advantages and limitations in comparison with clinical and neuroimaging data.
在急性神经疾病如全脑缺氧、缺血性或出血性中风以及创伤性脑损伤中,对S-100B的评估反映了症状的严重程度和预后。然而,S-100B释放的时间模式取决于损伤的部位、强度和病理生理学,例如创伤性脑损伤后神经元组织急性破坏导致的立即释放,或缺血性中风后血脑屏障逐渐破坏起关键作用的延迟释放。在慢性脑部疾病中,关于S-100B定量的临床价值的知识稀缺,需要进一步评估。本综述考虑了S-100B测量的两种情况,并与临床和神经影像学数据相比说明了其优点和局限性。