From the Departments of Neurosurgery (T.B.M., D.L.H., M.A.M.), Biomedical Engineering (T.B.M.), Cell Biology, Neurobiology and Anatomy (T.B.M.), Biophysics (B.D.G.), and Neurology (M.A.M.), Medical College of Wisconsin, Milwaukee; National Institute of Nursing Research (J.M.G.), NIH, Bethesda; Johns Hopkins School of Nursing and Medicine (J.M.G.), Baltimore, MD; Department of Physical Medicine and Rehabilitation (P.P.), Uniformed Services University of the Health Sciences, Bethesda, MD; Michigan Concussion Center (S.P.B.), University of Michigan, Ann Arbor; Department of Psychiatry (T.W.M.), Indiana University School of Medicine, Indianapolis; Department of Epidemiology and Biostatistics (J.H.), School of Public Health-Bloomington, Indiana University.
Neurology. 2024 Jan 23;102(2):e207991. doi: 10.1212/WNL.0000000000207991. Epub 2023 Dec 15.
The objective was to characterize the acute effects of concussion (a subset of mild traumatic brain injury) on serum interleukin (IL)-6 and IL-1 receptor antagonist (RA) and 5 additional inflammatory markers in athletes and military service academy members from the Concussion Assessment, Research, and Education Consortium and to determine whether these markers aid in discrimination of concussed participants from controls.
Athletes and cadets with concussion and matched controls provided blood at baseline and postinjury visits between January 2015 and March 2020. Linear models investigated changes in inflammatory markers measured using Meso Scale Discovery assays across time points (baseline and 0-12, 12-36, 36-60 hours). Subanalyses were conducted in participants split by sex and injury population. Logistic regression analyses tested whether acute levels of IL-6 and IL-1RA improved discrimination of concussed participants relative to brain injury markers (glial fibrillary acidic protein, tau, neurofilament light, ubiquitin c-terminal hydrolase-L1) or clinical data (Sport Concussion Assessment Tool-Third Edition, Standardized Assessment of Concussion, Balance Error Scoring System).
Participants with concussion (total, N = 422) had elevated IL-6 and IL-1RA at 0-12 hours vs controls (n = 345; IL-6: mean difference [MD] (standard error) = 0.701 (0.091), < 0.0001; IL-1RA: MD = 0.283 (0.042), < 0.0001) and relative to baseline (IL-6: MD = 0.656 (0.078), < 0.0001; IL-1RA: MD = 0.242 (0.038), < 0.0001), 12-36 hours (IL-6: MD = 0.609 (0.086), < 0.0001; IL-1RA: MD = 0.322 (0.041), < 0.0001), and 36-60 hours (IL-6: MD = 0.818 (0.084), < 0.0001; IL-1RA: MD = 0.317 (0.040), < 0.0001). IL-6 and IL-1RA were elevated in participants with sport (IL-6: MD = 0.748 (0.115), < 0.0001; IL-1RA: MD = 0.304 (0.055), < 0.0001) and combative-related concussions (IL-6: MD = 0.583 (0.178), = 0.001; IL-1RA: MD = 0.312 (0.081), = 0.0001). IL-6 was elevated in male (MD = 0.734 (0.105), < 0.0001) and female participants (MD = 0.600 (0.177), = 0.0008); IL-1RA was only elevated in male participants (MD = 0.356 (0.047), < 0.0001). Logistic regression showed the inclusion of IL-6 and IL-1RA at 0-12 hours improved the discrimination of participants with concussion from controls relative to brain injury markers (χ(2) = 17.855, = 0.0001; area under the receiver operating characteristic curve [AUC] 0.73 [0.66-0.80] to 0.78 [0.71-0.84]), objective clinical measures (balance and cognition; χ(2) = 40.661, < 0.0001; AUC 0.81 [0.76-0.86] to 0.87 [0.83-0.91]), and objective and subjective measures combined (χ(2) = 13.456, = 0.001; AUC 0.97 [0.95-0.99] to 0.98 [0.96-0.99]), although improvement in AUC was only significantly relative to objective clinical measures.
IL-6 and IL-1RA (male participants only) are elevated in the early-acute window postconcussion and may aid in diagnostic decisions beyond traditional blood markers and common clinical measures. IL-1RA results highlight sex differences in the immune response to concussion which should be considered in future biomarker work.
本研究旨在描述(轻度创伤性脑损伤的子集)脑震荡对运动员和军事院校学员血清白细胞介素(IL)-6 和 IL-1 受体拮抗剂(IL-1RA)及其他 5 种炎症标志物的急性影响,并确定这些标志物是否有助于区分脑震荡参与者和对照组。
2015 年 1 月至 2020 年 3 月期间,脑震荡组和对照组的运动员和学员在基线和受伤后访视时提供血液样本。使用 Meso Scale Discovery 检测法,线性模型研究了炎症标志物在各时间点(基线和 0-12 小时、12-36 小时、36-60 小时)的变化情况。亚组分析在按性别和损伤人群分组的参与者中进行。逻辑回归分析测试了 IL-6 和 IL-1RA 在急性水平下相对于脑损伤标志物(神经丝轻链、胶质纤维酸性蛋白、tau、泛素 C 端水解酶 L1)或临床数据(运动性脑震荡评估工具第三版、标准化脑震荡评估、平衡错误评分系统)的区分能力。
脑震荡组(n = 422)的 IL-6 和 IL-1RA 在 0-12 小时内高于对照组(n = 345;IL-6:平均差异(MD)(标准误差)= 0.701(0.091), < 0.0001;IL-1RA:MD = 0.283(0.042), < 0.0001),与基线相比(IL-6:MD = 0.656(0.078), < 0.0001;IL-1RA:MD = 0.242(0.038), < 0.0001),12-36 小时(IL-6:MD = 0.609(0.086), < 0.0001;IL-1RA:MD = 0.322(0.041), < 0.0001)和 36-60 小时(IL-6:MD = 0.818(0.084), < 0.0001;IL-1RA:MD = 0.317(0.040), < 0.0001)。运动(IL-6:MD = 0.748(0.115), < 0.0001;IL-1RA:MD = 0.304(0.055), < 0.0001)和格斗相关脑震荡(IL-6:MD = 0.583(0.178), = 0.001;IL-1RA:MD = 0.312(0.081), < 0.0001)参与者的 IL-6 和 IL-1RA 升高。男性(MD = 0.734(0.105), < 0.0001)和女性参与者(MD = 0.600(0.177), = 0.0008)的 IL-6 升高,男性参与者的 IL-1RA 升高(MD = 0.356(0.047), < 0.0001)。逻辑回归显示,0-12 小时内 IL-6 和 IL-1RA 的纳入提高了脑震荡参与者与对照组之间的区分能力,相对于脑损伤标志物( = 0.0001;曲线下面积(AUC)0.73 [0.66-0.80] 至 0.78 [0.71-0.84])、客观临床指标(平衡和认知; = 0.0001;AUC 0.81 [0.76-0.86] 至 0.87 [0.83-0.91])和客观及主观指标综合( = 0.001;AUC 0.97 [0.95-0.99] 至 0.98 [0.96-0.99]),尽管 AUC 的改善仅与客观临床指标显著相关。
脑震荡后的早期急性窗口期,IL-6 和 IL-1RA(仅男性参与者)升高,可能有助于做出超出传统血液标志物和常见临床指标的诊断决策。IL-1RA 结果突出了性别对脑震荡免疫反应的影响,在未来的生物标志物研究中应加以考虑。