A future blood test for acute traumatic spinal cord injury

被引:2
作者
Azad, Tej D. [1 ]
Ran, Kathleen R. [1 ,5 ]
Liu, Jiaqi [2 ]
Vattipally, Vikas N. [1 ]
Khela, Harmon [3 ]
Leite, Enzo [4 ]
Materi, Joshua D. [1 ]
Davidar, A. Daniel [1 ]
Bettegowda, Chetan [1 ]
Theodore, Nicholas [1 ]
机构
[1] Johns Hopkins Univ Hosp, Dept Neurosurg, Baltimore, MD USA
[2] Georgetown Univ, Sch Med, Washington, DC USA
[3] Univ Penn, Perelman Sch Med, Dept Neurosurg, Philadelphia, PA USA
[4] Fac Pernambucana Saude FPS, Recife, PE, Brazil
[5] Johns Hopkins Univ Hosp, Dept Neurosurg, 600 N Wolfe st, Baltimore, MD 21287 USA
关键词
Biomarkers; liquid biopsy; spinal cord injury; NEURON-SPECIFIC ENOLASE; CIRCULATING TUMOR DNA; CEREBROSPINAL-FLUID; PLASMA DNA; SURGICAL DECOMPRESSION; PROGNOSTIC MARKER; STRUCTURAL BIOMARKERS; INTRASPINAL PRESSURE; SERUM-LEVELS; NF-H;
D O I
10.1080/1354750X.2023.2298650
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Acute spinal cord injury (SCI) requires prompt diagnosis and intervention to minimize the risk of permanent neurologic deficit. Presently, SCI diagnosis and interventional planning rely on magnetic resonance imaging (MRI), which is not always available or feasible for severely injured patients. Detection of disease-specific biomarkers in biofluids via liquid biopsy may provide a more accessible and objective means of evaluating patients with suspected SCI. Cell-free DNA, which has been used for diagnosing and monitoring oncologic disease, may detect damage to spinal cord neurons via tissue-specific methylation patterns. Other types of biomarkers, including proteins and RNA species, have also been found to reflect neuronal injury and may be included as part of a multi-analyte assay to improve liquid biopsy performance. The feasibility of implementing liquid biopsy into current practices of SCI management is supported by the relative ease of blood sample collection as well as recent advancements in droplet digital polymerase chain reaction technology. In this review, we detail the current landscape of biofluid biomarkers for acute SCI and propose a framework for the incorporation of a putative blood test into the clinical management of SCI.
引用
收藏
页码:703 / 713
页数:11
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