中国神经再生研究(英文版) ›› 2025, Vol. 20 ›› Issue (5): 1399-1340.doi: 10.4103/NRR.NRR-D-23-01907

• 观点:视神经损伤修复保护与再生 • 上一篇    下一篇

创伤性脑损伤的可视化:诊断和评估的视觉线索

  

  • 出版日期:2025-05-15 发布日期:2024-10-30

Visualizing traumatic brain injury: ocular clues for diagnosis and assessment

Morteza Abyadeh, Vivek Gupta, Yuyi You, Joao A. Paulo, Mehdi Mirzaei *    

  1. ProGene Technologies Pty Ltd, Sydney, NSW, Australia (Abyadeh M)  Department of Clinical Medicine, Faculty of Medicine, Health and Human Sciences, Macquarie Medical School, Macquarie University, Macquarie Park, North Ryde, Sydney, NSW, Australia (Gupta V, You Y, Mirzaei M)  Department of Cell Biology, Harvard Medical School, Boston, MA, USA (Paulo JA) 
  • Online:2025-05-15 Published:2024-10-30
  • Contact: Mehdi Mirzaei, PhD, Mehdi.mirzaei@mq.edu.au

摘要: https://orcid.org/0000‐0001‐8727‐4984 (Mehdi Mirzaei) 

Abstract: Traumatic brain injury (TBI) is defined as damage to the brain resulting from an external sudden physical force or shock to the head. It is considered a silent public health epidemic causing significant death and disability globally. There were 64,000 TBI related deaths reported in the USA in 2020, with about US$76 billion in direct and indirect medical costs annually. TBI may have devastating chronic effects on the brain even if clinical symptoms disappear in the short term after the injury. TBI survivors have reported experiencing a range of neuropsychiatric symptoms such as amnesia, varying degrees of visual impairment, and have a higher risk of developing neurodegenerative diseases including Alzheimer’s disease (AD) later in their lives (Ramos-Cejudo et al., 2018). TBI has been shown to induce long-term neuropathological changes in the brain including amyloid‐β (Aβ) deposition and neurofibrillary tangle (NFT) formatton (Ramos‐Cejudo et al., 2018). Exposure to severe concussion or TBI has been suggested to increase the risk of AD development up to 4.5- fold. It can contribute to progressive cognitive decline which may be evident a decade affer the inittal injury depending on various factors such as sex, age, intensity, and site of injury (Tsitsopoulos and Marklund, 2013; National Academies of Sciences, Engineering, and Medicine, et al., 2019). Current diagnostic tools have their limitations, especially in detecttng mild forms of TBI, without clinical manifestattons. Advances in neuroimaging techniques such as positron emission tomography and cerebral spinal ffuid evaluatton have provided a valuable plattorm to study brain changes in TBI and associated neurodegeneration. However, ttme consuming and expensive nature of positron emission tomography and invasive cerebral spinal fluid sampling protocols limit their wide applicability in community setttngs. Given that any successful intervention to protect the neurons must be applied before a significant damage has occurred, it is imperattve to improve the existtng diagnostic approaches to detect milder forms of TBI.