Arterial Spin Labeling Reveals Elevated Cerebral Blood Flow with Distinct Clusters of Hypo- and Hyperperfusion after Traumatic Brain Injury

脑血流 创伤性脑损伤 白质 磁共振成像 医学 心脏病学 灌注 动脉自旋标记 内科学 脑灌注压 体素 灌注扫描 放射科 精神科
作者
Linda Xu,Jeffrey B. Ware,Junghoon Kim,Pashtun Shahim,Erika Silverman,Brigid Magdamo,Cian Dabrowski,Leroy Wesley,My Duyen Le,Justin Morrison,Hannah Zamore,Cillian Lynch,Dmitriy Petrov,H. Isaac Chen,James M. Schuster,Ramon Diaz‐Arrastia,Danielle K. Sandsmark
出处
期刊:Journal of Neurotrauma [Mary Ann Liebert]
卷期号:38 (18): 2538-2548 被引量:9
标识
DOI:10.1089/neu.2020.7553
摘要

Imaging detection of brain perfusion alterations after traumatic brain injury (TBI) may provide prognostic insights. In this study, we used arterial spin labeling (ASL) to quantify cross-sectional and longitudinal changes in cerebral blood flow (CBF) after TBI and correlated changes with clinical outcome. We analyzed magnetic resonance imaging scans from adult participants with TBI requiring hospitalization in the acute (2 weeks post-injury, n = 33) and chronic (6 months post-injury, n = 16) phases, with 13 participants scanned longitudinally at both time points. We also analyzed 18 age- and sex-matched healthy controls. Whole-brain CBF maps were derived using a three-dimensional pseudo-continuous arterial spin label technique. Mean CBF across tissue-based regions (whole brain, gray matter, and white matter) was compared cross-sectionally and longitudinally. In addition, individual-level clusters of abnormal perfusion were identified using voxel-based z-score analysis of relative CBF maps, and number and volume of abnormally hypo- and hyperperfused clusters were assessed cross-sectionally and longitudinally. Finally, all CBF measures were correlated with clinical outcome measures. Mean global and gray matter CBF were significantly elevated in acute and chronic TBI participants compared to controls. Participants with better outcome at 6 months post-injury tended to have higher CBF in the acute phase compared to those with poorer outcome. Acute TBI participants had a significantly greater volume of hypo- and hyperperfused brain tissue compared to controls, with these regions partially normalizing by the chronic phase. Our findings demonstrate global elevation of CBF with focal hypo- and hyperperfusion in the early post-injury period and suggest a reparative role for acute elevation in CBF post-TBI.
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