Walter Alexa E, Savalia Krupa, Yoon Jason, Morrison Justin, Schneider Andrea L C, Diaz-Arrastia Ramon, Sandsmark Danielle K
Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Departments of Neurology and Neurological Surgery, University of California Davis, Davis, California, USA.
Neurotrauma Rep. 2024 Jul 31;5(1):738-748. doi: 10.1089/neur.2024.0026. eCollection 2024.
Enlarged perivascular spaces (EPVs) can be seen on magnetic resonance imaging (MRI) scans in various neurological diseases, including traumatic brain injury (TBI). EPVs have been associated with cognitive dysfunction and sleep disturbances; however, their clinical significance remains unclear. The goal of this study was to identify MRI burden of EPVs over time following TBI and to explore their relationship with postinjury outcomes. Individuals with TBI underwent postinjury data collection at Day 1 (blood), 2 weeks (blood, MRI, outcomes), and 6 months (blood, MRI, outcomes). EPV burden was assessed using T1 and FLAIR sequences on representative slices in the centrum semiovale, basal ganglia, and midbrain. Serum blood was assayed to measure concentrations of neurofilament light (NfL) and glial fibrillary acidic protein (GFAP). Thirty-two participants with TBI were included (mean age 36.8 years, 78% male, 50% White). Total EPVs count did not significantly change from 2 weeks (23.5 [95% confidence interval or CI = 22.0-32.0]) to 6 months (26.0 [95% CI = 22.0-30.0], = 0.16). For self-reported measures of sleep, there were no significant associations between EPVs count and Insomnia Severity Index (2 weeks: β = -0.004; 95% CI = -0.094, 0.086; 6 months: β = 0.002; 95% CI = -0.122, 0.125) or the subset of sleep questions on the Rivermead Post-Concussion Symptoms Questionnaire (2 weeks: β = -0.005; 95% CI = -0.049, 0.039; 6 months: β = -0.019; 95% CI = -0.079, 0.042). Functional outcome, determined by 6 months incomplete recovery (Glasgow Outcome Scale-Extended [GOS-E < 8]) versus complete recovery (GOS-E = 8), was significantly associated with a higher number of EPVs at 2 weeks (odds ratio = 0.94, 95% CI = 0.88-0.99). Spearman correlations showed no significant relationship between EPVs count and GFAP or NfL. This study used commonly acquired MRI sequences to quantify EPVs and investigated their utility as a potential imaging biomarker in TBI. Given the minimal change in EPVs over time, this period may not be long enough for potential recovery or may indicate that EPVs are structural findings that do not significantly change over time.
在包括创伤性脑损伤(TBI)在内的各种神经系统疾病的磁共振成像(MRI)扫描中,可以看到血管周围间隙扩大(EPV)。EPV与认知功能障碍和睡眠障碍有关;然而,它们的临床意义仍不清楚。本研究的目的是确定TBI后随时间推移EPV的MRI负担,并探讨它们与伤后结局的关系。TBI患者在第1天(血液)、2周(血液、MRI、结局)和6个月(血液、MRI、结局)进行伤后数据收集。使用半卵圆中心、基底神经节和中脑代表性切片上的T1和FLAIR序列评估EPV负担。检测血清血以测量神经丝轻链(NfL)和胶质纤维酸性蛋白(GFAP)的浓度。纳入了32名TBI参与者(平均年龄36.8岁,78%为男性,50%为白人)。EPV总数从2周时的23.5[95%置信区间或CI = 22.0 - 32.0]到6个月时的26.0[95%CI = 22.0 - 30.0]没有显著变化(P = 0.16)。对于自我报告的睡眠测量,EPV计数与失眠严重程度指数之间没有显著关联(2周:β = -0.004;95%CI = -0.094,0.086;6个月:β = 0.002;95%CI = -0.122,0.125),也与Rivermead脑震荡后症状问卷中的睡眠问题子集没有显著关联(2周:β = -0.005;95%CI = -0.049,0.039;6个月:β = -0.019;95%CI = -0.079,0.042)。由6个月时不完全恢复(扩展格拉斯哥结局量表[GOS - E < 8])与完全恢复(GOS - E = 8)确定的功能结局与2周时较高的EPV数量显著相关(优势比 = 0.94,95%CI = 0.88 - 0.99)。Spearman相关性显示EPV计数与GFAP或NfL之间没有显著关系。本研究使用常用的MRI序列来量化EPV,并研究它们作为TBI潜在成像生物标志物的效用。鉴于EPV随时间变化极小,这段时间可能不足以实现潜在恢复,或者可能表明EPV是不会随时间显著变化的结构发现。