1 Department of Neurology, Miller School of Medicine, University of Miami , Miami, Florida.
2 Department of Medicine, Neuroscience and MRI Research Program, John A. Burns School of Medicine, University of Hawaii at Manoa , Honolulu, Hawaii.
J Neurotrauma. 2018 Mar 1;35(5):739-749. doi: 10.1089/neu.2016.4944. Epub 2018 Feb 9.
Traumatic brain injury (TBI) alters the lives of millions of people every year. Although mortality rates have improved, attributed to better pre-hospital care and reduction of secondary injury in the critical care setting, improvements in functional outcomes post-TBI have been difficult to achieve. Diffusion-tensor imaging (DTI) allows detailed measurement of microstructural damage in regional brain tissue post-TBI, thus improving our understanding of the extent and severity of TBI. Twenty subjects were recruited from a neurological intensive care unit and compared to 18 healthy control subjects. Magnetic resonance imaging (MRI) scanning was performed on a 3.0-Tesla Siemens TIM Trio Scanner (Siemens Medical Solutions, Erlangen, Germany) including T1- and T2-weighted sequences and DTI. Images were processed using DTIStudio software. SAS (SAS Institute Inc., Cary, NC) was used for statistical analysis of group differences in 14 brain regions (25 regions of interests [ROIs]). Seventeen TBI subjects completed scanning. TBI and control subjects did not differ in age or sex. All TBI subjects had visible lesions on structural MRI. TBI subjects had seven brain regions (nine ROIs) that showed significant group differences on DTI metrics (fractional anisotropy, radial diffusion, or mean diffusion) compared to noninjured subjects, including the corpus callosum (genu and splenium), superior longitudinal fasciculus, internal capsule, right retrolenticular internal capsule, posterior corona radiata, and thalamus. However, 16 ROIs showed relatively normal DTI measures. Quantitative DTI demonstrates multiple areas of microstructual injury in specific normal-appearing white matter brain regions. DTI may be useful for assessing the extent of brain injury in patients with early moderate to severe TBI.
创伤性脑损伤(TBI)每年都会改变数百万人的生活。尽管由于更好的院前护理和重症监护环境中继发性损伤的减少,死亡率有所改善,但 TBI 后的功能结果改善却难以实现。弥散张量成像(DTI)允许对 TBI 后区域性脑组织的微观结构损伤进行详细测量,从而提高我们对 TBI 程度和严重性的理解。从神经重症监护病房招募了 20 名受试者,并与 18 名健康对照受试者进行了比较。在 3.0 特斯拉西门子 TIM Trio 扫描仪(德国西门子医疗解决方案公司)上进行磁共振成像(MRI)扫描,包括 T1 和 T2 加权序列和 DTI。使用 DTIStudio 软件处理图像。SAS(SAS Institute Inc.,Cary,NC)用于 14 个脑区(25 个感兴趣区[ROI])的组间差异的统计分析。17 名 TBI 受试者完成了扫描。TBI 和对照组在年龄和性别上没有差异。所有 TBI 受试者的结构 MRI 上均可见病变。与未受伤的受试者相比,TBI 受试者的 7 个脑区(9 个 ROI)的 DTI 指标(各向异性分数、径向扩散或平均扩散)存在显著的组间差异,包括胼胝体(膝部和压部)、上纵束、内囊、右侧豆状核后内囊、后放射冠和丘脑。然而,16 个 ROI 显示出相对正常的 DTI 测量值。定量 DTI 显示特定正常表现的白质脑区存在多处微观结构损伤。DTI 可能有助于评估早期中重度 TBI 患者的脑损伤程度。