Progressive Neurodegeneration Across Chronic Stages of Severe Traumatic Brain Injury.

Zorry Belchev, Asaf Gilboa, Malcolm Binns, Brenda Colella, Joanna Glazer, David J Mikulis, Robin E Green
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引用次数: 5

Abstract

Objective: To examine the trajectory of structural gray matter changes across 2 chronic periods of recovery in individuals who have sustained severe traumatic brain injury (TBI), adding to the growing literature indicating that neurodegenerative processes occur in the months to years postinjury.

Participants: Patients who experienced posttraumatic amnesia of 1 hour or more, and/or scored 12 or less on the Glasgow Coma Scale at the emergency department or the scene of the accident, and/or had positive brain imaging findings were recruited while receiving inpatient care, resulting in 51 patients with severe TBI.

Methods: Secondary analyses of gray matter changes across approximately 5 months, 1 year, and 2.5 years postinjury were undertaken, using an automated segmentation protocol with improved accuracy in populations with morphological anomalies. We compared patients and matched controls on regions implicated in poorer long-term clinical outcome (accumbens, amygdala, brainstem, hippocampus, thalamus). To model brain-wide patterns of change, we then conducted an exploratory principal component analysis (PCA) on the linear slopes of all regional volumes across the 3 time points. Finally, we assessed nonlinear trends across earlier (5 months-1 year) versus later (1-2.5 years) time-windows with PCA to compare degeneration rates across time. Chronic degeneration was predicted cortically and subcortically brain-wide, and within specific regions of interest.

Results: (1) From 5 months to 1 year, patients showed significant degeneration in the accumbens, and marginal degeneration in the amygdala, brainstem, thalamus, and the left hippocampus when examined unilaterally, compared with controls. (2) PCA components representing subcortical and temporal regions, and regions from the basal ganglia, significantly differed from controls in the first time-window. (3) Progression occurred at the same rate across both time-windows, suggesting neither escalation nor attenuation of degeneration across time.

Conclusion: Localized yet progressive decline emphasizes the necessity of developing interventions to offset degeneration and improve long-term functioning.

严重创伤性脑损伤慢性阶段的进行性神经变性。
目的:研究严重创伤性脑损伤(TBI)患者在2个慢性恢复期的结构灰质变化轨迹,并补充越来越多的文献表明,神经退行性过程发生在损伤后的几个月到几年。参与者:在急诊科或事故现场经历了1小时或更长时间的创伤后失忆,和/或格拉斯哥昏迷评分为12分或更低,和/或有阳性脑成像结果的患者在接受住院治疗时被招募,导致51例严重TBI患者。方法:对损伤后约5个月、1年和2.5年的灰质变化进行二次分析,采用自动分割方案,提高了形态学异常人群的准确性。我们比较了与较差的长期临床结果相关的区域(伏隔核、杏仁核、脑干、海马体、丘脑)的患者和对照组。为了模拟全脑变化模式,我们随后对3个时间点上所有区域体积的线性斜率进行了探索性主成分分析(PCA)。最后,我们用PCA评估了早期(5个月1年)和后期(1-2.5年)时间窗的非线性趋势,以比较不同时间的退化率。慢性变性预测皮质和皮质下全脑,并在特定区域感兴趣。结果:(1)5个月~ 1年,与对照组相比,单侧检查时,患者伏隔核出现明显变性,杏仁核、脑干、丘脑、左侧海马出现边缘性变性。(2)在第一个时间窗内,代表皮层下和颞区以及基底神经节区域的PCA成分与对照组显著不同。(3)在两个时间窗口中,退化以相同的速率发生,表明退化既不随时间增加,也不随时间衰减。结论:局部进行性衰退强调了开发干预措施以抵消退变和改善长期功能的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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