Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA; Brain and Spinal Injury Center, Zuckerberg San Francisco General Hospital, San Francisco, CA, USA.
Department of Radiology, University of California San Francisco, San Francisco, CA, USA; Brain and Spinal Injury Center, Zuckerberg San Francisco General Hospital, San Francisco, CA, USA.
Lancet Neurol. 2019 Oct;18(10):953-961. doi: 10.1016/S1474-4422(19)30282-0. Epub 2019 Aug 23.
After traumatic brain injury (TBI), plasma concentration of glial fibrillary acidic protein (GFAP) correlates with intracranial injury visible on CT scan. Some patients with suspected TBI with normal CT findings show pathology on MRI. We assessed the discriminative ability of GFAP to identify MRI abnormalities in patients with normal CT findings.
TRACK-TBI is a prospective cohort study that enrolled patients with TBI who had a clinically indicated head CT scan within 24 h of injury at 18 level 1 trauma centres in the USA. For this analysis, we included patients with normal CT findings (Glasgow Coma Scale score 13-15) who consented to venepuncture within 24 h post injury and who had an MRI scan 7-18 days post injury. We compared MRI findings in these patients with those of orthopaedic trauma controls and healthy controls recruited from the study sites. Plasma GFAP concentrations (pg/mL) were measured using a prototype assay on a point-of-care platform. We used receiver operating characteristic (ROC) analysis to evaluate the discriminative ability of GFAP for positive MRI scans in patients with negative CT scans over 24 h (time between injury and venepuncture). The primary outcome was the area under the ROC curve (AUC) for GFAP in patients with CT-negative and MRI-positive findings versus patients with CT-negative and MRI-negative findings within 24 h of injury. The Dunn Kruskal-Wallis test was used to compare GFAP concentrations between MRI lesion types with Benjamini-Hochberg correction for multiple comparisons. This study is registered with ClinicalTrials.gov, number NCT02119182.
Between Feb 26, 2014, and June 15, 2018, we recruited 450 patients with normal head CT scans (of whom 330 had negative MRI scans and 120 had positive MRI scans), 122 orthopaedic trauma controls, and 209 healthy controls. AUC for GFAP in patients with CT-negative and MRI-positive findings versus patients with CT-negative and MRI-negative findings was 0·777 (95% CI 0·726-0·829) over 24 h. Median plasma GFAP concentration was highest in patients with CT-negative and MRI-positive findings (414·4 pg/mL, 25-75th percentile 139·3-813·4), followed by patients with CT-negative and MRI-negative findings (74·0 pg/mL, 17·5-214·4), orthopaedic trauma controls (13·1 pg/mL, 6·9-20·0), and healthy controls (8·0 pg/mL, 3·0-14·0; all comparisons between patients with CT-negative MRI-positive findings and other groups p<0·0001).
Analysis of blood GFAP concentrations using prototype assays on a point-of-care platform within 24 h of injury might improve detection of TBI and identify patients who might need subsequent MRI and follow-up.
National Institute of Neurological Disorders and Stroke and US Department of Defense.
颅脑创伤(TBI)后,血浆中胶质纤维酸性蛋白(GFAP)的浓度与 CT 扫描可见的颅内损伤相关。一些疑似 TBI 但 CT 检查结果正常的患者在 MRI 上存在病变。我们评估了 GFAP 识别 CT 检查正常的 TBI 患者 MRI 异常的能力。
TRACK-TBI 是一项前瞻性队列研究,在美国 18 个 1 级创伤中心纳入了在受伤后 24 小时内有临床指征进行头部 CT 扫描的 TBI 患者。在这项分析中,我们纳入了 CT 检查正常(格拉斯哥昏迷量表评分 13-15 分)、在受伤后 24 小时内行静脉穿刺且在受伤后 7-18 天行 MRI 扫描并同意静脉穿刺的患者。我们比较了这些患者的 MRI 检查结果与从研究地点招募的骨科创伤对照组和健康对照组的结果。使用床边即时检验平台上的原型检测方法测量血浆 GFAP 浓度(pg/mL)。我们使用受试者工作特征(ROC)分析来评估 24 小时内(从受伤到静脉穿刺) GFAP 对 CT 阴性但 MRI 阳性的患者进行阳性 MRI 扫描的鉴别能力。主要结局是 24 小时内 CT 阴性、MRI 阳性患者与 CT 阴性、MRI 阴性患者的 ROC 曲线下面积(AUC)。使用 Dunn 克鲁斯卡尔-沃利斯检验比较 MRI 病变类型之间的 GFAP 浓度,并使用 Benjamini-Hochberg 校正进行多重比较。本研究在 ClinicalTrials.gov 注册,编号为 NCT02119182。
在 2014 年 2 月 26 日至 2018 年 6 月 15 日期间,我们纳入了 450 例 CT 检查正常的患者(其中 330 例 MRI 检查阴性,120 例 MRI 检查阳性)、122 例骨科创伤对照组和 209 例健康对照组。在 24 小时内 CT 阴性、MRI 阳性患者与 CT 阴性、MRI 阴性患者的 AUC 为 0.777(95%CI 0.726-0.829)。CT 阴性、MRI 阳性患者的中位血浆 GFAP 浓度最高(414.4 pg/mL,25-75 分位 139.3-813.4),其次是 CT 阴性、MRI 阴性患者(74.0 pg/mL,17.5-214.4)、骨科创伤对照组(13.1 pg/mL,6.9-20.0)和健康对照组(8.0 pg/mL,3.0-14.0;所有与 CT 阴性、MRI 阳性患者比较的组间差异均 p<0.0001)。
在受伤后 24 小时内使用床边即时检验平台分析血液 GFAP 浓度可能有助于提高 TBI 的检出率,并识别可能需要进一步 MRI 检查和随访的患者。
美国国立神经病学和中风研究所和美国国防部。