Hermanides Jeroen, Hong Young T, Trivedi Monica, Outtrim Joanne, Aigbirhio Franklin, Nestor Peter J, Guilfoyle Matthew, Winzeck Stefan, Newcombe Virginia F J, Das Tilak, Correia Marta M, Carpenter Keri L H, Hutchinson Peter J A, Gupta Arun K, Fryer Tim D, Pickard John D, Menon David K, Coles Jonathan P
University Division of Anaesthesia, University of Cambridge, Cambridge, UK.
Wolfson Brain Imaging Centre, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Brain. 2021 Dec 16;144(11):3492-3504. doi: 10.1093/brain/awab255.
Metabolic derangements following traumatic brain injury are poorly characterized. In this single-centre observational cohort study we combined 18F-FDG and multi-tracer oxygen-15 PET to comprehensively characterize the extent and spatial pattern of metabolic derangements. Twenty-six patients requiring sedation and ventilation with intracranial pressure monitoring following head injury within a Neurosciences Critical Care Unit, and 47 healthy volunteers were recruited. Eighteen volunteers were excluded for age over 60 years (n = 11), movement-related artefact (n = 3) or physiological instability during imaging (n = 4). We measured cerebral blood flow, blood volume, oxygen extraction fraction, and 18F-FDG transport into the brain (K1) and its phosphorylation (k3). We calculated oxygen metabolism, 18F-FDG influx rate constant (Ki), glucose metabolism and the oxygen/glucose metabolic ratio. Lesion core, penumbra and peri-penumbra, and normal-appearing brain, ischaemic brain volume and k3 hotspot regions were compared with plasma and microdialysis glucose in patients. Twenty-six head injury patients, median age 40 years (22 male, four female) underwent 34 combined 18F-FDG and oxygen-15 PET at early, intermediate, and late time points (within 24 h, Days 2-5, and Days 6-12 post-injury; n = 12, 8, and 14, respectively), and were compared with 20 volunteers, median age 43 years (15 male, five female) who underwent oxygen-15, and nine volunteers, median age 56 years (three male, six female) who underwent 18F-FDG PET. Higher plasma glucose was associated with higher microdialysate glucose. Blood flow and K1 were decreased in the vicinity of lesions, and closely related when blood flow was <25 ml/100 ml/min. Within normal-appearing brain, K1 was maintained despite lower blood flow than volunteers. Glucose utilization was globally reduced in comparison with volunteers (P < 0.001). k3 was variable; highest within lesions with some patients showing increases with blood flow <25 ml/100 ml/min, but falling steeply with blood flow lower than 12 ml/100 ml/min. k3 hotspots were found distant from lesions, with k3 increases associated with lower plasma glucose (Rho -0.33, P < 0.001) and microdialysis glucose (Rho -0.73, P = 0.02). k3 hotspots showed similar K1 and glucose metabolism to volunteers despite lower blood flow and oxygen metabolism (P < 0.001, both comparisons); oxygen extraction fraction increases consistent with ischaemia were uncommon. We show that glucose delivery was dependent on plasma glucose and cerebral blood flow. Overall glucose utilization was low, but regional increases were associated with reductions in glucose availability, blood flow and oxygen metabolism in the absence of ischaemia. Clinical management should optimize blood flow and glucose delivery and could explore the use of alternative energy substrates.
创伤性脑损伤后的代谢紊乱情况目前仍缺乏充分的特征描述。在这项单中心观察性队列研究中,我们结合了18F-FDG和多示踪剂氧-15正电子发射断层扫描(PET),以全面描述代谢紊乱的程度和空间模式。我们招募了26名在神经科学重症监护病房因头部受伤需要镇静、通气并进行颅内压监测的患者,以及47名健康志愿者。18名志愿者因年龄超过60岁(n = 11)、与运动相关的伪影(n = 3)或成像过程中的生理不稳定(n = 4)而被排除。我们测量了脑血流量、血容量、氧摄取分数、18F-FDG向脑内的转运(K1)及其磷酸化(k3)。我们计算了氧代谢、18F-FDG流入速率常数(Ki)、葡萄糖代谢以及氧/葡萄糖代谢比。将患者的病变核心、半暗带和半暗带周围区域、外观正常的脑区、缺血性脑体积和k3热点区域与血浆和微透析葡萄糖进行了比较。26名头部受伤患者,中位年龄40岁(22名男性,4名女性)在伤后早期、中期和晚期(伤后24小时内、第2 - 5天、第6 - 12天;分别为n = 12、8和14)接受了34次18F-FDG和氧-15 PET联合检查,并与20名接受氧-15检查的志愿者(中位年龄43岁,15名男性,5名女性)以及9名接受18F-FDG PET检查的志愿者(中位年龄56岁,3名男性,6名女性)进行了比较。较高的血浆葡萄糖与较高的微透析葡萄糖相关。病变附近的血流量和K1降低,当血流量<25 ml/100 ml/min时两者密切相关。在外观正常的脑区内,尽管血流量低于志愿者,但K1仍保持稳定。与志愿者相比,葡萄糖利用率总体降低(P < 0.001)。k3存在差异;在病变内最高,一些患者在血流量<25 ml/100 ml/min时k3升高,但当血流量低于12 ml/100 ml/min时急剧下降。在远离病变处发现了k3热点,k3升高与较低的血浆葡萄糖(Rho -0.33,P < 0.001)和微透析葡萄糖(Rho -0.73,P = 0.02)相关。尽管血流量和氧代谢较低,但k3热点的K1和葡萄糖代谢与志愿者相似(两项比较P均< 0.001);与缺血一致的氧摄取分数增加并不常见。我们发现葡萄糖输送依赖于血浆葡萄糖和脑血流量。总体葡萄糖利用率较低,但局部增加与葡萄糖可用性、血流量和氧代谢在无缺血情况下的降低相关。临床管理应优化血流量和葡萄糖输送,并可探索使用替代能量底物。