1Department of Physical Medicine and Rehabilitation, Harvard Medical School, Spaulding Rehabilitation Hospital, and Home Base, a Red Sox Foundation and Massachusetts General Hospital Program, Boston, Massachusetts.
2Department of Biology, Emory University, Atlanta, Georgia.
J Neurotrauma. 2019 Aug 15;36(16):2400-2406. doi: 10.1089/neu.2018.6341. Epub 2019 Apr 23.
Neurofilament light (NF-L) might have diagnostic and prognostic potential as a blood biomarker for mild traumatic brain injury (mTBI). However, elevated NF-L is associated with several neurological disorders associated with older age, which could confound its usefulness as a traumatic brain injury biomarker. We examined whether NF-L is elevated differentially following uncomplicated mTBI in older adults with pre-injury neurological disorders. In a case-control study, a sample of 118 adults (mean age = 62.3 years, standard deviation [SD] = 22.5, range = 18-100; 52.5% women) presenting to the emergency department (ED) with an uncomplicated mTBI were enrolled. All participants underwent head computed tomography in the ED and showed no macroscopic evidence of injury. The mean time between injury and blood sampling was 8.3 h (median [Md] = 3.5; SD = 13.5; interquartile range [IQR] = 1.9-6.0, range = 0.8-67.4, and 90% collected within 19 h). A sample of 40 orthopedically-injured trauma control subjects recruited from a second ED also were examined. Serum NF-L levels were measured and analyzed using Human Neurology 4-Plex A assay on a HD-1 Single Molecule Array (Simoa) instrument. A high correlation was found between age and NF-L levels in the total mTBI sample (r = 0.80), within the subgroups without pre-injury neurological diseases (r = 0.76) and with pre-injury neurological diseases (r = 0.68), and in the trauma control subjects (r = 0.76). Those with mTBIs and pre-injury neurological conditions had higher NF-L levels than those with no pre-injury neurological conditions ( < 0.001, Cohen's d = 1.01). Older age and pre-injury neurological diseases are associated with elevated serum NF-L levels in patients with head trauma and in orthopedically-injured control subjects.
神经丝轻链(NF-L)作为一种血液生物标志物,可能具有诊断和预后轻度创伤性脑损伤(mTBI)的潜力。然而,NF-L 升高与几种与年龄较大相关的神经退行性疾病有关,这可能使其作为创伤性脑损伤生物标志物的用途复杂化。我们研究了 NF-L 是否在有神经退行性疾病的老年患者发生无并发症 mTBI 后存在差异升高。在病例对照研究中,纳入了 118 名因无并发症 mTBI 就诊于急诊科(ED)的成年人(平均年龄 62.3 岁,标准差 [SD] 22.5,范围 18-100;52.5%为女性)。所有患者均在 ED 行头部计算机断层扫描,无明显的损伤迹象。受伤和采血之间的平均时间为 8.3 小时(中位数 [Md] 3.5;SD 13.5;四分位间距 [IQR] 1.9-6.0,范围 0.8-67.4,90%在 19 小时内采集)。还检查了从另一个 ED 招募的 40 名骨科损伤的创伤对照组。使用 HD-1 单分子阵列(Simoa)仪器上的 Human Neurology 4-Plex A 测定法测量并分析血清 NF-L 水平。在总 mTBI 样本中,年龄与 NF-L 水平之间存在高度相关性(r=0.80),在无既往神经疾病亚组(r=0.76)和有既往神经疾病亚组(r=0.68)中,以及在创伤对照组(r=0.76)中也是如此。与无既往神经疾病的患者相比,有 mTBI 和既往神经疾病的患者 NF-L 水平更高( <0.001,Cohen's d=1.01)。在有头部创伤和骨科损伤的对照组患者中,年龄较大和既往神经疾病与血清 NF-L 水平升高有关。