From the Monash-Epworth Rehabilitation Research Centre (A.J.H., J.L.P., G.S.), Turner Institute for Brain and Mental Health, School of Psychological Sciences, and Department of Neuroscience (A.J.H., B.S., S.R.S., W.P., M.L., G.S.), Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton; Department of Neurology (B.S.), Alfred Health, Melbourne, Australia; Health and Human Services (S.S.), Vancouver Island University, Nanaimo; Division of Medical Sciences (S.S.), University of Victoria, British Columbia, Canada; NIA-Layton Oregon Aging & Alzheimer's Disease Research Center (L.C.S., D.L.S.), Oregon Health & Science University; Department of Neurology (L.C.S.), Portland Veterans Affairs Health Care System; Advanced Imaging Research Center (D.L.S.), Oregon Health & Science University, Portland; Department of Molecular Imaging and Therapy (C.C.R.), Austin Health, Heidelberg; Florey Department of Neuroscience and Mental Health (C.C.R.), University of Melbourne, Parkville; and Department of Radiology (M.L.), Alfred Health, Melbourne, Australia.
Neurology. 2023 Jul 4;101(1):e63-e73. doi: 10.1212/WNL.0000000000207370. Epub 2023 May 8.
Enlarged perivascular spaces (ePVS) have been identified as a key signature of glymphatic system dysfunction in neurologic conditions. The incidence and clinical implications of ePVS after traumatic brain injury (TBI) are not yet understood. We investigated whether individuals with chronic moderate-to-severe TBI had an increased burden of ePVS and whether ePVS burden is modulated by the presence of focal lesions, older brain age, and poorer sleep quality. We examined whether an increased burden of ePVS was associated with poorer cognitive and emotional outcomes.
Using a cross-sectional design, participants with a single moderate-to-severe chronic TBI (sustained ≥10 years ago) were recruited from an inpatient rehabilitation program. Control participants were recruited from the community. Participants underwent 3T brain MRI, neuropsychological assessment, and clinical evaluations. ePVS burden in white matter was quantified using automated segmentation. The relationship between the number of ePVS, group membership, focal lesions, brain age, current sleep quality, and outcome was modeled using negative binomial and linear regressions.
This study included 100 participants with TBI (70% male; mean age = 56.8 years) and 75 control participants (54.3% male; mean age = 59.8 years). The TBI group had a significantly greater burden of ePVS (prevalence ratio rate [PRR] = 1.29, = 0.013, 95% CI 1.05-1.57). The presence of bilateral lesions was associated with greater ePVS burden (PRR = 1.41, = 0.021, 95% CI 1.05-1.90). There was no association between ePVS burden, sleep quality (PRR = 1.01, = 0.491, 95% CI 0.98-1.048), and sleep duration (PRR = 1.03, = 0.556, 95% CI 0.92-1.16). ePVS was associated with verbal memory (β = -0.42, = 0.006, 95% CI -0.72 to -0.12), but not with other cognitive domains. The burden of ePVS was not associated with emotional distress (β = -0.70, = 0.461, 95% CI -2.57 to 1.17) or brain age (PRR = 1.00, = 0.665, 95% CI 0.99-1.02).
TBI is associated with a greater burden of ePVS, especially when there have been bilateral brain lesions. ePVS was associated with reduced verbal memory performance. ePVS may indicate ongoing impairments in glymphatic system function in the chronic postinjury period.
在神经疾病中,扩大的血管周围空间(ePVS)已被确定为血-脑屏障功能障碍的关键特征。外伤性脑损伤(TBI)后 ePVS 的发生率及其临床意义尚不清楚。我们研究了慢性中重度 TBI 患者是否存在 ePVS 负担增加的情况,以及 ePVS 负担是否受到局灶性病变、脑老化和睡眠质量差的调节。我们还研究了 ePVS 负担增加是否与认知和情绪结局较差有关。
采用横断面设计,从住院康复计划中招募了一名患有单一中重度慢性 TBI(≥ 10 年前发生)的患者。对照组参与者从社区招募。参与者接受了 3T 脑部 MRI、神经心理学评估和临床评估。使用自动分割技术对白质中的 ePVS 负担进行量化。使用负二项回归和线性回归模型,研究 ePVS 数量与组别的关系、局灶性病变、脑龄、当前睡眠质量和结局之间的关系。
本研究纳入了 100 名 TBI 患者(70%为男性;平均年龄为 56.8 岁)和 75 名对照组参与者(54.3%为男性;平均年龄为 59.8 岁)。TBI 组 ePVS 负担明显增加(患病率比[PRR]为 1.29, = 0.013,95%置信区间为 1.05-1.57)。双侧病变的存在与更大的 ePVS 负担相关(PRR = 1.41, = 0.021,95%置信区间为 1.05-1.90)。ePVS 负担与睡眠质量(PRR = 1.01, = 0.491,95%置信区间为 0.98-1.048)和睡眠时间(PRR = 1.03, = 0.556,95%置信区间为 0.92-1.16)之间无关联。ePVS 与言语记忆(β = -0.42, = 0.006,95%置信区间为-0.72 至-0.12)相关,但与其他认知领域无关。ePVS 负担与情绪困扰(β = -0.70, = 0.461,95%置信区间为-2.57 至 1.17)或脑龄(PRR = 1.00, = 0.665,95%置信区间为 0.99-1.02)无关。
TBI 与更大的 ePVS 负担有关,特别是当存在双侧脑病变时。ePVS 与言语记忆能力下降有关。ePVS 可能表明在慢性损伤后时期,血-脑屏障功能障碍仍在持续。