Fluid Biomarkers for Chronic Traumatic Encephalopathy

被引:12
|
作者
Shahim, Pashtun [1 ,2 ,3 ,4 ,5 ]
Gill, Jessica M. [3 ]
Blennow, Kaj [1 ,2 ]
Zetterberg, Henrik [1 ,2 ,6 ,7 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, S-43180 Molndal, Sweden
[2] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[3] NIH, Bldg 10, Bethesda, MD 20892 USA
[4] Ctr Neurosci & Regenerat Med CNRM, Bethesda, MD USA
[5] Henry M Jackson Fdn Adv Mil Med, Bethesda, MD USA
[6] UCL Queen Sq Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[7] UCL, UK Dementia Res Inst, London, England
关键词
biomarkers; cerebrospinal fluid; concussion; chronic traumatic encephalopathy; plasma; serum; neurofilament; tau; SPECTRIN BREAKDOWN PRODUCTS; SERUM NEUROFILAMENT LIGHT; ALPHA-II-SPECTRIN; BRAIN-INJURY; CEREBROSPINAL-FLUID; ICE HOCKEY; NEUROCHEMICAL AFTERMATH; BLOOD BIOMARKERS; TAU PROTEINS; EXOSOMAL TAU;
D O I
10.1055/s-0040-1715095
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic traumatic encephalopathy (CTE) is a neuropathological condition that has been described in individuals who have been exposed to repetitive head impacts, including concussions and subconcussive trauma. Currently, there is no fluid or imaging biomarker for diagnosing CTE during life. Based on retrospective clinical data, symptoms of CTE include changes in behavior, cognition, and mood, and may develop after a latency phase following the injuries. However, these symptoms are often nonspecific, making differential diagnosis based solely on clinical symptoms unreliable. Thus, objective biomarkers for CTE pathophysiology would be helpful in understanding the course of the disease as well as in the development of preventive and therapeutic measures. Herein, we review the literature regarding fluid biomarkers for repetitive concussive and subconcussive head trauma, postconcussive syndrome, as well as potential candidate biomarkers for CTE. We also discuss technical challenges with regard to the current fluid biomarkers and potential pathways to advance the most promising biomarker candidates into clinical routine.
引用
收藏
页码:411 / 419
页数:9
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