1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
6 National Intrepid Center of Excellence, Walter Reed National Military Medical Center, Bethesda, Maryland.
J Neurotrauma. 2018 Oct 1;35(19):2250-2258. doi: 10.1089/neu.2018.5684. Epub 2018 Jun 7.
Magnetic resonance imaging (MRI) is a powerful tool for visualizing traumatic brain injury(TBI)-related lesions. Trauma-induced encephalomalacia is frequently identified by its hyperintense appearance on fluid-attenuated inversion recovery (FLAIR) sequences. In addition to parenchymal lesions, TBI commonly results in cerebral microvascular injury, but its anatomical relationship to parenchymal encephalomalacia is not well characterized. The current study utilized a multi-modal MRI protocol to assess microstructural tissue integrity (by mean diffusivity [MD] and fractional aniosotropy [FA]) and altered vascular function (by cerebral blood flow [CBF] and cerebral vascular reactivity [CVR]) within regions of visible encephalomalacia and normal appearing tissue in 27 chronic TBI (minimum 6 months post-injury) subjects. Fifteen subjects had visible encephalomalacias whereas 12 did not have evident lesions on MRI. Imaging from 14 age-matched healthy volunteers were used as controls. CBF was assessed by arterial spin labeling (ASL) and CVR by measuring the change in blood-oxygen-level-dependent (BOLD) MRI during a hypercapnia challenge. There was a significant reduction in FA, CBF, and CVR with a complementary increase in MD within regions of FLAIR-visible encephalomalacia (p < 0.05 for all comparisons). In normal-appearing brain regions, only CVR was significantly reduced relative to controls (p < 0.05). These findings indicate that vascular dysfunction represents a TBI endophenotype that is distinct from structural injury detected using conventional MRI, may be present even in the absence of visible structural injury, and persists long after trauma. CVR may serve as a useful diagnostic and pharmacodynamic imaging biomarker of traumatic microvascular injury.
磁共振成像(MRI)是一种强大的工具,可用于可视化外伤性脑损伤(TBI)相关病变。创伤性脑软化通常因其在液体衰减反转恢复(FLAIR)序列上的高信号表现而被识别。除了实质病变外,TBI 还常导致脑微血管损伤,但它与实质脑软化的解剖学关系尚未得到很好的描述。本研究利用多模态 MRI 方案评估了 27 例慢性 TBI(伤后至少 6 个月)患者中可见脑软化区域和正常外观组织内的微观结构组织完整性(通过平均弥散度[MD]和分数各向异性[FA])和改变的血管功能(通过脑血流[CBF]和脑血管反应性[CVR])。15 名受试者可见脑软化灶,而 12 名受试者 MRI 未见明显病变。14 名年龄匹配的健康志愿者的影像作为对照。通过动脉自旋标记(ASL)评估 CBF,通过测量高碳酸血症挑战期间血氧水平依赖(BOLD)MRI 的变化来评估 CVR。FLAIR 可见脑软化区域的 FA、CBF 和 CVR 显著降低,MD 互补增加(所有比较均为 p<0.05)。在正常外观的脑区,仅 CVR 与对照组相比显著降低(p<0.05)。这些发现表明,血管功能障碍代表 TBI 表型,与使用常规 MRI 检测的结构损伤不同,即使在没有可见结构损伤的情况下也可能存在,并且在创伤后很长时间内仍然存在。CVR 可能是外伤性微血管损伤的有用诊断和药效动力学成像生物标志物。