MRS Detects Metabolic Dysfunction after Brain Injury

MRS 检测脑损伤后代谢功能障碍

• 批准号: 7029334
• 负责人: Paul M Vespa
• 金额: $ 31.73万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-01-10 至 2009-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7029334
• 关键词: aerobiosis; aspartate; biomarker; brain injury; brain metabolism; brain morphology; cell death; clinical research; human subject; metabolism disorder; microdialysis; mitochondrial disease /disorder; neuropsychological tests; nuclear magnetic resonance spectroscopy; patient oriented research; positron emission tomography

DESCRIPTION (provided by applicant): The main aim of this proposal is to determine if mitochondria! dysfunction as reflected by low rates of oxidative metabolism is predictive of eventual brain volume loss after traumatic brain injury (TBI). TBI is a condition of widespread brain dysfunction in which secondary cell death and brain atrophy occur in normal appearing tissue despite a relatively confined area of primary anatomical damage. The mechanism of delayed brain atrophy is not clear but may be related to early and persistent impaired oxidative metabolism that is endemic after TBI. Reduced oxidative metabolism (CMRO2) is a result of impaired mitochondrial function and has been measured in TBI by positron emission tomography (PET). Our preliminary studies indicate that 1) CMRO2 is reduced in normal appearing brain regions as well as adjacent to contusions, 2) reduction in CMRO2 in normal regions can be monitored by cerebral microdialysis lactate/pyruvate values, 3) delayed atrophy is related to the duration of abnormal lactate/pyruvate values, and 4) delayed atrophy is related to neurologic/cognitive outcome. Hence, a persistent deficit in energy supply may be related to eventual cell loss and poor outcome. TBI provides a unique opportunity to study human brain tissue with invasive cerebral microdialysis monitoring and PET imaging, thus enabling independent measurements of mitochondrial function in space (PET) and across time (microdialysis). The proposed studies will 1) Determine the magnitude and spatial distribution of impaired oxidative metabolism after TBI using PET and microdialysis, 2) Determine if brain regions of reduced oxidative metabolism are destined for brain atrophy on follow-up MR), 3) Determine if acute impaired oxidative metabolism corresponds to poor clinical outcome, 4) Evaluate the validity of magnetic resonance spectroscopy N-Acetyl-Aspartate as a non-invasive surrogate marker of oxidative metabolism. The fourth aim is intended to be exploratory but could lead to widespread application of MRS in clinical care for TBI patients in centers lacking oxygen PET technology. This study can only be done within the context of traumatic brain injury, in which invasive monitoring methods are standard of care. The knowledge from the proposed studies will have widespread application to critical care of neurotrauma patients.

描述（由申请人提供）：本提案的主要目的是确定线粒体！由低氧化代谢率反映的功能障碍预示着创伤性脑损伤（TBI）后最终的脑体积损失。TBI是一种广泛的脑功能障碍的病症，其中继发性细胞死亡和脑萎缩发生在正常外观的组织中，尽管原发性解剖损伤的区域相对有限。迟发性脑萎缩的机制尚不清楚，但可能与TBI后流行的早期和持续的氧化代谢受损有关。氧化代谢减少（CMRO 2）是线粒体功能受损的结果，并已通过正电子发射断层扫描（PET）在TBI中进行了测量。我们的初步研究表明：1）CMRO 2在正常出现的脑区域以及邻近挫伤的脑区域中减少，2）正常区域中CMRO 2的减少可以通过脑微透析乳酸/丙酮酸值监测，3）延迟性萎缩与异常乳酸/丙酮酸值的持续时间相关，4）延迟性萎缩与神经/认知结果相关。因此，持续的能量供应不足可能与最终的细胞丢失和不良结局有关。TBI提供了一个独特的机会，研究人脑组织与侵入性脑微透析监测和PET成像，从而使独立的测量线粒体功能的空间（PET）和跨时间（微透析）。所提出的研究将1）使用PET和微透析确定TBI后氧化代谢受损的程度和空间分布，2）确定氧化代谢降低的脑区域是否注定在随访MR时发生脑萎缩，3）确定急性氧化代谢受损是否对应于不良临床结果，4）评估磁共振波谱N-乙酰天冬氨酸作为氧化代谢的非侵入性替代标记物的有效性。第四个目标是探索性的，但可能导致MRS在缺乏氧气PET技术的中心的TBI患者的临床护理中的广泛应用。这项研究只能在创伤性脑损伤的背景下进行，其中侵入性监测方法是护理标准。从拟议的研究中获得的知识将广泛应用于神经创伤患者的重症监护。