Biomechanics of Pediatric Head Injury

小儿头部损伤的生物力学

• 批准号: 8113731
• 负责人: Susan Sheps Margulies
• 金额: $ 5.18万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-05-15 至 2012-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8113731
• 关键词: Acute; Address; Adult; Age; Air; Anatomy; Animal Experiments; Animal Model; Animals; Attenuated; Back; Behavior; Behavioral; Biochemical; Biomechanics; Brain; Brain Injuries; Brain Stem; Cause of Death; Cell Death; Cerebral perfusion pressure; Cerebrovascular Circulation; Cerebrum; Child; Childhood; Childhood Injury; Clinical; Clinical Research; Cognitive; Computer Simulation; Contusions; Craniocerebral Trauma; Data; Diffuse; Edema; Etiology; Event; Family suidae; Folate; Folic Acid; Foundations; Free Radical Scavengers; Free Radicals; Frequencies; Funding; Goals; Head; Homeostasis; Human; Hypoxia; Infant; Injury; Interdisciplinary Study; Intervention; Intracranial Hemorrhages; Intracranial Pressure; Ischemic Brain Injury; Laboratory Finding; Measures; Mechanics; Mediating; Microscopic; Microspheres; Modeling; Motion; Motor; Multiple Head Injuries; Nerve Degeneration; Newborn Infant; Optics; Outcome; Pattern; Preparation; Prevention; Prevention strategy; Recovery; Recovery of Function; Research; Research Personnel; Respiratory Insufficiency; Resuscitation; Risk; Rotation; Saline; Severities; Signal Pathway; Signal Transduction; Simulate; Spatial Distribution; Spectrum Analysis; Supplementation; Swelling; Testing; Time; Tissues; Toddler; Translational Research; Traumatic Brain Injury; Unconscious State; animal tissue; base; brain tissue; clinically relevant; experience; functional outcomes; improved; injured; injury prevention; instrument; neuropathology; nitrone; novel; pressure; programs; repaired; research study; response; treatment strategy; white matter

DESCRIPTION (provided by applicant): Traumatic brain injury is the most common cause of death in childhood, yet etiology and treatment of pediatric head injuries remain controversial. Previously, we established an interdisciplinary research paradigm using acute animal experiments, biomechanical tissue tests, retrospective clinical studies, anthropomorphic "doll" studies, and computational simulations. Our data show that children do indeed have injury mechanisms that are distinct from the adult, and require age-specific injury prevention strategies and treatments. In this competitive renewal, we build on the foundation we have established, both to deepen our understanding of basic injury mechanisms and to enhance the clinical relevance of our findings. We will supplement our current platforms with novel preparations - survival studies, porcine behavioral outcomes, cerebral blood flow (CBF) measures, post-injury respiratory insufficiency, and injury treatment studies - to enhance translation of research findings from the laboratory to the clinical setting. Our overall hypothesis is that rapid rotations of the immature brain without impact produce brain injury via both mechanical and biochemical signals, resulting in sustained functional and histological abnormalities. We will compare long-term outcomes after single and multiple head injuries to determine if injury interval modulates injury severity and if axonal injury is reduced with folate supplementation (Aim 1). We will use human computational models to extend our animal studies to cyclic shaking motions to estimate contribution of harmonic amplification to injury risk (Aim 2). Using animal experiments and computer models, we will identify cerebral strains associated with rapid regional decreases in CBF and brainstem deformations associated with loss of cerebral autoregulation (Aim 3). We will modulate regional deformations by altering rotation direction, and endothelial response with hypertonic saline to validate acute mechanical and biochemical signaling pathways. In piglets with respiratory insufficiency after head injury (Aim 4), we hypothesize that resuscitation with 100% FiO2 results in exacerbated neuropathology mediated by free radical release, and we will compare outcomes with room air and 100% FiO2, as well as with and without free radical scavengers to verify functionality. The proposed studies address our long-term goal of elucidating injury mechanisms and potential treatment strategies for traumatic brain injuries in children.

描述（由申请人提供）：创伤性脑损伤是儿童最常见的死亡原因，然而儿童脑损伤的病因和治疗仍然存在争议。在此之前，我们通过急性动物实验、生物力学组织测试、回顾性临床研究、拟人化“娃娃”研究和计算模拟建立了跨学科的研究范式。我们的数据表明，儿童确实有不同于成人的伤害机制，需要针对年龄的伤害预防策略和治疗。在这个竞争性的更新中，我们建立在我们已经建立的基础上，既加深了我们对基本损伤机制的理解，又增强了我们研究结果的临床相关性。我们将用新的制剂——生存研究、猪行为结果、脑血流量（CBF）测量、损伤后呼吸功能不全和损伤治疗研究——来补充我们现有的平台，以加强研究成果从实验室到临床的转化。我们的总体假设是，未成熟的大脑在没有冲击的情况下快速旋转会通过机械和生化信号产生脑损伤，导致持续的功能和组织学异常。我们将比较单次和多次头部损伤后的长期结果，以确定损伤间隔是否调节损伤严重程度，以及叶酸补充是否减轻轴索损伤（目的1）。我们将使用人类计算模型将我们的动物研究扩展到循环振动运动，以估计谐波放大对损伤风险的贡献（目标2）。通过动物实验和计算机模型，我们将确定与CBF快速区域减少和脑干变形相关的脑应变与大脑自动调节功能丧失（目的3）。我们将通过改变旋转方向和高渗盐水内皮反应来调节局部变形，以验证急性机械和生化信号通路。对于头部损伤后呼吸功能不全的仔猪（Aim 4），我们假设100% FiO2复苏会导致自由基释放介导的神经病理恶化，我们将比较室内空气和100% FiO2以及使用和不使用自由基清除剂的结果，以验证其功能。提出的研究解决了我们阐明儿童创伤性脑损伤的损伤机制和潜在治疗策略的长期目标。