Association Between Traumatic Brain Injury and Cognitive Decline Among Middle-to-Older Aged Men in the Vietnam Era Twin Study of Aging.

IF 1.8 Q3 CLINICAL NEUROLOGY Neurotrauma reports Pub Date : 2024-06-17 eCollection Date: 2024-01-01 DOI:10.1089/neur.2024.0034
Alexander Ivan B Posis, John E Alcaraz, Humberto Parada, Aladdin H Shadyab, Jeremy A Elman, Matthew S Panizzon, Chandra A Reynolds, Carol E Franz, William S Kremen, Linda K McEvoy
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Abstract

Traumatic brain injury (TBI) is associated with increased risk of dementia. However, whether TBI is associated with greater cognitive decline over time in specific cognitive domains among older adults is not well understood. This prospective cohort study used data from 1476 male Vietnam Era Twin Study of Aging participants (average age at study entry = 57.9 years, range = 51-71 years; 97.6% non-Hispanic; 92.5% White) collected from 2003 to 2019, who had complete information on prior TBI. Participants completed a comprehensive neuropsychological assessment at up to three visits over up to a 12-year follow-up period during which they also self-reported their history of TBI. Multivariable, linear mixed-effects models were used to assess associations between TBI and cognitive performance trajectories. Effect measure modification by apolipoprotein E (APOE) epsilon 4 (ε4) genotype status was assessed in a subset of participants. Thirty-one percent of participants reported a history of TBI; 29.4% were APOE ε4 carriers. There were no statistically significant associations of TBI with decline in episodic memory, executive function, or processing speed among participants overall. In models stratified by APOE ε4 carrier status, TBI was associated with a larger magnitude of decline in executive function for APOE ε4 carriers (β = -0.0181; 95% confidence interval [CI] -0.0335, -0.0027) compared to noncarriers (β = -0.0031; 95% CI -0.0128, 0.0067; P Interaction = 0.03). In sensitivity analyses, TBI earlier in life (before military induction, average age = 20 years) was associated with faster declines in executive function compared to no TBI, irrespective of APOE ε4 status. In this sample of middle-to-older aged men, TBI was associated with faster declines in executive function among APOE ε4 carriers and among those who reported TBI in early life. These findings support the importance of a life course perspective when considering factors that may influence cognitive health in aging.

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越战时期老年双胞胎研究中中老年男性脑外伤与认知能力下降之间的关系
创伤性脑损伤(TBI)与痴呆症风险增加有关。然而,对于创伤性脑损伤是否会导致老年人在特定认知领域的认知能力随时间推移而下降,目前尚不十分清楚。这项前瞻性队列研究使用了从 2003 年到 2019 年收集的 1476 名男性越战时期老龄化双胞胎研究参与者(研究开始时的平均年龄 = 57.9 岁,范围 = 51-71 岁;97.6% 为非西班牙裔;92.5% 为白人)的数据,这些参与者都有关于之前 TBI 的完整信息。在长达 12 年的随访期间,受试者在最多三次的访问中完成了全面的神经心理学评估,在此期间,他们还自我报告了 TBI 病史。多变量线性混合效应模型用于评估创伤性脑损伤与认知表现轨迹之间的关联。在一部分参与者中评估了载脂蛋白 E(APOE)ε4(ε4)基因型状态对效果测量的影响。31%的参与者报告有创伤性脑损伤病史;29.4%为APOE ε4携带者。在总体参与者中,创伤性脑损伤与外显记忆、执行功能或处理速度的下降没有明显的统计学关联。在根据 APOE ε4 携带者状况进行分层的模型中,与非携带者相比(β = -0.0031; 95% CI -0.0128, 0.0067; P交互作用 = 0.03),APOE ε4携带者的创伤性脑损伤与执行功能下降的幅度更大(β = -0.0181; 95% 置信区间 [CI] -0.0335,-0.0027)。在敏感性分析中,无论 APOE ε4 状态如何,与未发生创伤性脑损伤相比,生命早期(入伍前,平均年龄 = 20 岁)的创伤性脑损伤与执行功能的快速下降有关。在这一中老年男性样本中,在 APOE ε4 携带者和早年曾报告过 TBI 的人中,TBI 与执行功能下降更快有关。这些发现证明,在考虑可能影响老年认知健康的因素时,从生命过程的角度看问题非常重要。
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