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P90?A systematic review of spinal cord serum and cerebrospinal fluid biomarkers for use in degenerative cervical myelopathy

机译:P90?对脊髓血清和脑脊液生物标志物进行系统审查,用于退行性颈椎病

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Whilst radiological evidence of compression is the hallmark of degenerative cervical myelopathy [DCM], it is unable to stage or prognosticate. Moreover, asymptomatic spinal cord compression is common and therefore new methods of assessing spinal cord function are required. We aimed to: 1) Evaluate the evidence-base for serum and CSF biomarkers of spinal cord damage in diagnosis, prognosis or predicting response to treatment in DCM 2) Identify serum and CSF biomarkers of spinal cord damage studied in other conditions, which may have relevance to DCM.Scoping review.Human only.A search of MEDLINE and EMBASE was performed. Studies involving DCM patients or biomarkers relevant to spinal cord pathobiology were included.852 results were screened, of which 83 were included. 9 studies explored 12 biomarkers in DCM. NFH (n=3), S100b and NSE (n=2) received most study. 74 studies explored a further 118 biomarkers in other conditions; S100b (n=13), NFH (n=11) and GFAP (n=10) received most study. Overall, 72 studies used targeted approaches, in which candidate biomarkers were chosen in advance. 11 used unbiased approaches, in which high throughput analyses identified candidate biomarkers during the study.The evidence-base for use of biomarkers in DCM is limited. Whilst targeted approaches have identified a number of candidate spinal cord markers, few have shown clinical utility. There is a shift towards investigating panels of multiple markers and unbiased, high-throughput approaches.
机译:虽然压缩的放射性证据是退行性颈椎病的标志,但它无法阶段或预后化。此外,无症状脊髓压缩是常见的,因此需要评估脊髓功能的新方法。我们的目标是:1)评估血清和CSF生物标志物的脊髓损伤的证据基础,DCM 2在DCM 2中治疗的治疗中的脊髓损伤损伤)鉴定血清和CSF生物标志物在其他条件下研究的脊髓损伤的脊髓损伤的生物标志物与DCM.COPIPT Review.human的相关性。在搜索Medline和Embase的搜索。包括DCM患者或与脊髓病理学病理学相关的生物标志物的研究包括筛选852个结果,其中包括其中83个。 9研究探讨了DCM中的12个生物标志物。 NFH(n = 3),S100B和NSE(n = 2)获得大多数研究。 74研究在其他条件下探讨了118个生物标志物; S100B(n = 13),NFH(n = 11)和GFAP(n = 10)接受大多数研究。总体而言,72项研究使用靶向方法,其中提前选择候选生物标志物。 11采用了非偏见的方法,其中高通量分析在研究期间确定了候选生物标志物。DCM中使用生物标志物的证据基础是有限的。虽然有针对性的方法已经确定了许多候选脊髓标记,但很少有临床效用。朝向调查多个标记和无偏见的高通量方法的调查面板的转变。

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