Kao Yu-Chieh Jill, Chen Seu-Hwa, Lu Chia-Feng, Hsieh Bao-Yu, Chen Cheng-Yu, Chang Ying-Chao, Huang Chao-Ching
Department of Biomedical Imaging and Radiological Sciences, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
Department of Anatomy and Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Brain Commun. 2021 Mar 26;3(2):fcab048. doi: 10.1093/braincomms/fcab048. eCollection 2021.
Hypoxic ischaemia encephalopathy is the major cause of brain injury in new-borns. However, to date, useful biomarkers which may be used to early predict neurodevelopmental impairment for proper commencement of hypothermia therapy is still lacking. This study aimed to determine whether the early neuroimaging characteristics and ultrastructural correlates were associated with different injury progressions and brain damage severity outcomes after neonatal hypoxic ischaemia. Longitudinal 7 T MRI was performed within 6 h, 24 h and 7 days after hypoxic ischaemia in rat pups. The brain damage outcome at 7 days post-hypoxic ischaemia assessed using histopathology and MRI were classified as mild, moderate and severe. We found there was a spectrum of different brain damage severity outcomes after the same duration of hypoxic ischaemia. The severity of brain damage determined using MRI correlated well with that assessed by histopathology. Quantitative MRI characteristics denoting water diffusivity in the tissue showed significant differences in the apparent diffusion coefficient deficit volume and deficit ratios within 6 h, at 24 h and 7 days after hypoxic ischaemia among the 3 different outcome groups. The susceptible brain areas to hypoxic ischaemia were revealed by the temporal changes in regional apparent diffusion coefficient values among three outcome groups. Within 6 h post-hypoxic ischaemia, a larger apparent diffusion coefficient deficit volume and deficit ratios and lower apparent diffusion coefficient values were highly associated with adverse brain damage outcome. In the apparent diffusion coefficient deficit areas detected early after hypoxic ischaemia which were highly associated with severe damage outcome, transmission electron microscopy revealed fragmented nuclei; swollen rough endoplasmic reticulum and degenerating mitochondria in the cortex and prominent myelin loss and axon detraction in the white matter. Taken together, different apparent diffusion coefficient patterns obtained early after hypoxic ischaemia are highly associated with different injury progression leading to different brain damage severity outcomes, suggesting the apparent diffusion coefficient characteristics may be applicable to early identify the high-risk neonates for hypothermia therapy.
缺氧缺血性脑病是新生儿脑损伤的主要原因。然而,迄今为止,仍缺乏可用于早期预测神经发育障碍以便适时开始低温治疗的有用生物标志物。本研究旨在确定新生儿缺氧缺血后早期神经影像学特征和超微结构相关性是否与不同的损伤进展及脑损伤严重程度结局相关。在新生大鼠缺氧缺血后6小时、24小时和7天内进行了纵向7T磁共振成像(MRI)。使用组织病理学和MRI评估缺氧缺血后7天的脑损伤结局,并分为轻度、中度和重度。我们发现,在相同时长的缺氧缺血后存在一系列不同的脑损伤严重程度结局。使用MRI确定的脑损伤严重程度与组织病理学评估结果高度相关。表示组织中水分子扩散率的定量MRI特征显示,在3个不同结局组中,缺氧缺血后6小时、24小时和7天时,表观扩散系数缺损体积和缺损率存在显著差异。通过三个结局组区域表观扩散系数值的时间变化揭示了对缺氧缺血敏感的脑区。缺氧缺血后6小时内,较大的表观扩散系数缺损体积和缺损率以及较低的表观扩散系数值与不良脑损伤结局高度相关。在缺氧缺血后早期检测到的与严重损伤结局高度相关的表观扩散系数缺损区域,透射电子显微镜显示皮质中有核碎裂、粗面内质网肿胀和线粒体退化,白质中有明显的髓鞘丢失和轴突脱失。综上所述,缺氧缺血后早期获得的不同表观扩散系数模式与导致不同脑损伤严重程度结局的不同损伤进展高度相关,这表明表观扩散系数特征可能适用于早期识别低温治疗的高危新生儿。