Lyall Donald M, Russell Emma R, Ward Joey, Stewart William
School of Health and Wellbeing, University of Glasgow, Glasgow G12 8TB, Scotland, UK.
School of Psychology and Neuroscience, University of Glasgow, Glasgow G12 8QB, Scotland, UK.
Brain Commun. 2024 Oct 11;6(6):fcae363. doi: 10.1093/braincomms/fcae363. eCollection 2024.
Traumatic brain injury (TBI) is a risk factor for neurodegenerative disease. We currently have no means to identify patients most at risk of neurodegenerative disease following injury and, resultantly, no means to target risk mitigation interventions. To address this, we explored the association between history of traumatic brain injury with cognitive performance and imaging measures of white matter integrity. From the UK Biobank imaging sub-study ( = 50 376), participants were identified with either self-reported ( = 177) or health record coded broad- (injury codes; = 1096) or narrow-band (TBI specific codes; = 274) TBI, or as controls with no such documented history ( = 49 280). Cognitive scores and imaging measures of corpus callosum white matter integrity were compared between injury participants (versus no injury), corrected for age, sex, socioeconomic status and medications. TBI was associated with poorer cognitive and imaging phenotypes. The strongest deleterious associations were for narrow-band injury ( difference 0.2-0.3; < 0.01). All cognitive and imaging phenotypes were strongly inter-correlated ( < 0.001). This study provides insight into possible early biomarkers predating neurodegenerative disease following brain injury. Measures of cognition and white matter following injury may provide means to identify individuals most at risk of neurodegenerative disease, to which mitigation strategies might be targeted.
创伤性脑损伤(TBI)是神经退行性疾病的一个风险因素。目前,我们尚无办法识别受伤后最易患神经退行性疾病的患者,因此也无法针对风险缓解干预措施。为解决这一问题,我们探讨了创伤性脑损伤史与认知表现以及白质完整性成像指标之间的关联。在英国生物银行成像子研究(n = 50376)中,通过自我报告(n = 177)或健康记录编码的广义(损伤编码;n = 1096)或狭义(TBI特定编码;n = 274)TBI识别出参与者,或作为无此类记录史的对照者(n = 49280)。在对年龄、性别、社会经济地位和药物进行校正后,比较了受伤参与者(与未受伤者相比)的认知得分和胼胝体白质完整性的成像指标。TBI与较差的认知和成像表型相关。最强的有害关联是狭义损伤(差异0.2 - 0.3;p < 0.01)。所有认知和成像表型都高度相互关联(p < 0.001)。本研究为脑损伤后神经退行性疾病之前可能的早期生物标志物提供了见解。受伤后的认知和白质测量指标可能提供手段来识别最易患神经退行性疾病的个体,缓解策略可能针对这些个体。