轻度脑外伤患者磁共振成像 T2 弛豫测量的个体水平分析:脑部炎症的可能迹象

IF 3.4 2区 医学 Q2 NEUROIMAGING Neuroimage-Clinical Pub Date : 2024-01-01 DOI:10.1016/j.nicl.2024.103647
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引用次数: 0

摘要

轻度创伤性脑损伤(mTBI),通常称为脑震荡,是一种普遍存在的疾病,会对人的健康、功能和福祉产生重大影响。目前的临床实践依赖于自我报告的症状来指导有关恢复运动、就业和教育的决策。遗憾的是,依赖主观评估可能无法准确反映神经病理的恢复情况,从而增加了 mTBI 患者再次发生头部创伤的风险。目前还没有客观的技术来评估脑组织微观结构的改变,而这种改变正是 mTBI 的特征。基于核磁共振成像的 T2 弛豫是一种定量成像技术,可检测大脑中的液体特性,并被假定为神经炎症的信号。本研究旨在探讨个体水平的 T2 弛豫测量法在评估 mTBI 造成的细胞损伤方面的潜力。本研究招募了 20 名患有急性运动相关 mTBI(伤后 14 天内)的男性参与者和 44 名健康对照者。采用虚假发现率校正的体素Z检验法,将每位mTBI参与者的体素T2弛豫图与健康对照组的平均值进行对比分析。五名受试者在临床康复后接受了重新扫描,并将扫描结果与其急性 T2 驰豫图进行比较,以评估潜在神经炎症的减少情况。与健康对照组相比,19/20(95%)名 mTBI 参与者的 T2 松弛时间明显增加,区域包括海马、额叶皮层、顶叶皮层、岛叶、扣带回皮层和小脑。结果表明,mTBI 患者的脑液增多。纵向结果表明,所有五名参与者的 T2 松弛度都有所下降,这表明随着时间的推移可能会有所缓解。这项研究强调了个体水平的 T2 驰豫磁共振成像作为评估 mTBI 患者脑部细微病变的非侵入性方法的潜力。识别和监测脑内液体含量的变化有助于预测 mTBI 患者的恢复情况和制定个性化治疗计划。未来的研究应将这一测量方法与其他炎症标记物(如血液生物标记物)进行验证,以检验 T2-松弛测量法是否与 mTBI 患者的细微脑部炎症有关。此外,未来的研究应利用更大规模的对照组来建立标准范围,并计算出可靠的 z 值分析。
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Individual-level analysis of MRI T2 relaxometry in mild traumatic brain injury: Possible indications of brain inflammation

Mild traumatic brain injury (mTBI), often called concussion, is a prevalent condition that can have significant implications for people’s health, functioning and well-being. Current clinical practice relies on self-reported symptoms to guide decision-making regarding return to sport, employment, and education. Unfortunately, reliance on subjective evaluations may fail to accurately reflect the resolution of neuropathology, exposing individuals with mTBI to an increased risk of further head trauma. No objective technique currently exists to assess the microstructural alterations to brain tissue which characterise mTBI. MRI-based T2 relaxation is a quantitative imaging technique that is susceptible to detecting fluid properties in the brain and is hypothesised to indicate neuroinflammation. This study aimed to investigate the potential of individual-level T2 relaxometry to evaluate cellular damage from mTBI. 20 male participants with acute sports-related mTBI (within 14 days post-injury) and 44 healthy controls were recruited for this study. Each mTBI participant’s voxel-wise T2 relaxometry map was analysed against healthy control averages using a voxel-wise z-test with false discovery rate correction. Five participants were re-scanned after clinical recovery and results were compared to their acute T2 relaxometry maps to assess reduction in potential neuroinflammation. T2 relaxation times were significantly increased in 19/20 (95 %) mTBI participants compared to healthy controls, in regions including the hippocampus, frontal cortex, parietal cortex, insula, cingulate cortex and cerebellum. Results suggest the presence of increased cerebral fluid in individuals with mTBI. Longitudinal results indicated a reduction in T2 relaxation for all five participants, indicating a possible resolution over time. This research highlights the potential of individual-level T2 relaxometry MRI as a non-invasive method for assessing subtle brain pathology in mTBI. Identifying and monitoring changes in the fluid content in the brain could aid in predicting recovery and developing individualised treatment plans for individuals with mTBI. Future research should validate this measure with other markers of inflammation (e.g. from blood biomarkers) to test whether T2-relaxometry is related to subtle brain inflammation in mTBI. In addition, future research should utilise larger control groups to establish normative ranges and compute robust z-score analyses.

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来源期刊
Neuroimage-Clinical
Neuroimage-Clinical NEUROIMAGING-
CiteScore
7.50
自引率
4.80%
发文量
368
审稿时长
52 days
期刊介绍: NeuroImage: Clinical, a journal of diseases, disorders and syndromes involving the Nervous System, provides a vehicle for communicating important advances in the study of abnormal structure-function relationships of the human nervous system based on imaging. The focus of NeuroImage: Clinical is on defining changes to the brain associated with primary neurologic and psychiatric diseases and disorders of the nervous system as well as behavioral syndromes and developmental conditions. The main criterion for judging papers is the extent of scientific advancement in the understanding of the pathophysiologic mechanisms of diseases and disorders, in identification of functional models that link clinical signs and symptoms with brain function and in the creation of image based tools applicable to a broad range of clinical needs including diagnosis, monitoring and tracking of illness, predicting therapeutic response and development of new treatments. Papers dealing with structure and function in animal models will also be considered if they reveal mechanisms that can be readily translated to human conditions.
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