1 UCLA Brain Injury Research Center and Department of Neurosurgery, David Geffen School of Medicine at UCLA, Los Angeles, California.
2 UCLA Metabolomics Center, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Los Angeles, California.
J Neurotrauma. 2019 Jan 15;36(2):212-221. doi: 10.1089/neu.2018.5674. Epub 2018 Aug 13.
Treatment of severe traumatic brain injury (TBI) in the intensive care unit focuses on controlling intracranial pressure, ensuring sufficient cerebral perfusion, and monitoring for secondary injuries. However, there are limited prognostic tools and no biomarkers or tests of the evolving neuropathology. Metabolomics has the potential to be a powerful tool to indirectly monitor evolving dysfunctional metabolism. We compared metabolite levels in simultaneously collected arterial and jugular venous samples in acute TBI patients undergoing intensive care as well as in healthy control volunteers. Our results show that, first, many circulating metabolites are decreased in TBI patients compared with healthy controls days after injury; both proline and hydroxyproline were depleted by ≥60% compared with healthy controls, as was gluconate. Second, both arterial and jugular venous plasma metabolomic analysis separates TBI patients from healthy controls and shows that distinct combinations of metabolites are driving the group separation in the two blood types. Third, TBI patients under heavy sedation with pentobarbital at the time of blood collection were discernibly different from patients not receiving pentobarbital. These results highlight the importance of accounting for medications in metabolomics analysis. Jugular venous plasma metabolomics shows potential as a minimally invasive tool to identify and study dysfunctional cerebral metabolism after TBI.
在重症监护病房中,严重创伤性脑损伤(TBI)的治疗重点是控制颅内压、确保足够的脑灌注以及监测继发性损伤。然而,目前预后评估工具有限,也没有神经病理学进展的生物标志物或检测手段。代谢组学有可能成为一种间接监测不断变化的代谢功能障碍的强大工具。我们比较了同时采集的急性 TBI 患者和健康对照志愿者的动脉和颈内静脉样本中的代谢物水平。结果表明,首先,与健康对照组相比,TBI 患者在受伤后数天内许多循环代谢物的水平降低;与健康对照组相比,脯氨酸和羟脯氨酸分别减少了≥60%,葡萄糖酸盐也减少了。其次,动脉和颈内静脉血浆代谢组学分析可将 TBI 患者与健康对照组区分开来,并表明两种血液类型的组分离是由不同的代谢物组合驱动的。第三,在采集血液时接受戊巴比妥重度镇静的 TBI 患者与未接受戊巴比妥的患者明显不同。这些结果强调了在代谢组学分析中考虑药物的重要性。颈内静脉血浆代谢组学显示出作为一种微创工具的潜力,可用于识别和研究 TBI 后大脑代谢的功能障碍。