Biomarkers in spinal cord injury

被引:56
作者
Pouw, M. H. [1 ]
Hosman, A. J. F. [1 ]
van Middendorp, J. J. [1 ]
Verbeek, M. M. [2 ]
Vos, P. E. [3 ]
van de Meent, H. [4 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Orthoped Surg, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Inst Brain Cognit & Behav, Lab Pediat & Neurol, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6500 HB Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Rehabil Med, NL-6500 HB Nijmegen, Netherlands
关键词
biomarkers; spinal cord injury; cerebrospinal fluid; serum; trauma; NEURON-SPECIFIC ENOLASE; MYELIN BASIC-PROTEIN; CEREBROSPINAL-FLUID CONCENTRATIONS; FIBRILLARY ACIDIC PROTEIN; S-100; PROTEIN; BIOCHEMICAL MARKERS; S100-BETA PROTEIN; EVOKED-POTENTIALS; SERUM BIOMARKERS; BRAIN-INJURY;
D O I
10.1038/sc.2008.176
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study design: Literature review. Objectives: In traumatic spinal cord injury (SCI), much effort has been put into the evaluation of SCI severity and the prediction of recovery potential. An accurate prediction of the initial damage of the spinal cord that differentiates between the severities of SCI however, may help physicians in choosing a particular neuroprotective treatment in the acute phase. Neurochemical biomarkers may possibly fulfil these requirements. The aim of this review was to describe (1) the current status of neurochemical biomarkers in SCI; (2) their potential diagnostic role in SCI. Methods: MEDLINE was searched from 1966 to 2008 to identify publications concerning biomarkers in traumatic SCI. Results: The biomarkers S-100 beta, neuron-specific enolase, neurofilament light chain, and Glial fibrillary acidic protein are significantly increased in cases of (experimental) spinal cord injury. Furthermore, increased serum concentrations of S-100 beta have been correlated with an unfavourable functional outcome. Although biomarkers in SCI show promising results, considerations and shortcomings, such as polytrauma, haemolysis, extracerebral sources, and poor resuscitation, must be studied in greater detail before biomarkers can be utilised in the clinical care of SCI. Conclusions: Quantitative standards for determining the extent of SCI during the acute phase must be developed and validated. Even though increased concentrations of neurochemical biomarkers have been identified in patients with SCI, these do not yet provide a sensitive prognostic tool. Considering the limited availability of sensitive prognostic tools, neurochemical biomarkers of SCI should be evaluated and validated in future clinical trials. Spinal Cord (2009) 47, 519-525; doi: 10.1038/sc.2008.176; published online 20 January 2009
引用
收藏
页码:519 / 525
页数:7
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