Moody Jena N, Howard Erica, Nolan Kate E, Prieto Sarah, Logue Mark W, Hayes Jasmeet P
Department of Psychology, The Ohio State University, Columbus, Ohio, USA.
National Center for PTSD, VA Boston Healthcare System, Boston, Massachusetts, USA.
Neurotrauma Rep. 2024 Aug 22;5(1):760-769. doi: 10.1089/neur.2024.0048. eCollection 2024.
Traumatic brain injuries (TBIs) may increase the risk for Alzheimer's disease (AD) and its neuropathological correlates, although the mechanisms of this relationship are unclear. The current study examined the synergistic effects of TBI and genetic risk for AD on β-amyloid (Aβ) levels among Vietnam War Veterans. We hypothesized that the combination of TBI and higher polygenic risk score (PRS) for AD would be associated with lower cerebrospinal fluid (CSF) Aβ. Data were obtained from the Department of Defense Alzheimer's Disease Neuroimaging Initiative. Participants included Vietnam War Veterans without dementia who identified as White non-Hispanic/Latino and had available demographic, clinical assessment, genetic, and CSF biomarker data. Lifetime TBI history was assessed using The Ohio State University TBI Identification Method. Participants were categorized into those with and without TBI. Among those with a prior TBI, injury severity was defined as either mild or moderate/severe. CSF Aβ ratios were calculated. Genetic propensity for AD was assessed using PRSs. Hierarchical linear regression models examined the interactive effects of TBI and PRS for AD on Aβ. Exploratory analyses examined the interaction between TBI severity and PRS. The final sample included 88 male Vietnam War Veterans who identified as White non-Hispanic/Latino ( = 68.3 years), 49 of whom reported a prior TBI. There was a significant interaction between TBI and PRS, such that individuals with TBI and higher PRS for AD had lower Aβ ( = -0.45, 95% CI: -0.86 to -0.05, = 0.03). This relationship may be stronger with increasing TBI severity ( = 0.05). Overall, TBI was associated with lower Aβ, indicating greater amyloid deposition in the brain, in the context of greater polygenic risk for AD. These findings highlight may be at increased risk for AD neuropathology following TBI.
创伤性脑损伤(TBI)可能会增加患阿尔茨海默病(AD)及其神经病理学相关疾病的风险,尽管这种关系的机制尚不清楚。本研究调查了越战退伍军人中TBI与AD遗传风险对β-淀粉样蛋白(Aβ)水平的协同作用。我们假设TBI与较高的AD多基因风险评分(PRS)相结合会与较低的脑脊液(CSF)Aβ相关。数据来自国防部阿尔茨海默病神经影像倡议。参与者包括无痴呆症的越战退伍军人,他们为非西班牙裔/拉丁裔白人,且有可用的人口统计学、临床评估、基因和CSF生物标志物数据。使用俄亥俄州立大学TBI识别方法评估终生TBI病史。参与者被分为有TBI和无TBI两组。在有既往TBI的参与者中,损伤严重程度被定义为轻度或中度/重度。计算CSF Aβ比率。使用PRS评估AD的遗传倾向。分层线性回归模型研究了TBI和AD的PRS对Aβ的交互作用。探索性分析研究了TBI严重程度与PRS之间的相互作用。最终样本包括88名非西班牙裔/拉丁裔白人男性越战退伍军人(平均年龄 = 68.3岁),其中49人报告有既往TBI。TBI与PRS之间存在显著交互作用,即有TBI且AD的PRS较高的个体Aβ较低(β = -0.45,95%CI:-0.86至-0.05,P = 0.03)。随着TBI严重程度增加,这种关系可能更强(P = 0.05)。总体而言,在AD多基因风险较高的情况下,TBI与较低的Aβ相关,表明大脑中淀粉样蛋白沉积更多。这些发现凸显了TBI后AD神经病理学风险可能增加。