VA San Diego Healthcare System, San Diego, CA, USA; University of California San Diego, La Jolla, CA, USA.
Tramatic Brain Injury Center of Excellence, Silver Spring, MD, USA; Walter Reed National Military Medical Center, Bethesda, MD, USA; National Intrepid Center of Excellence, Bethesda, MD, USA; University of British Columbia, Vancouver, BC, Canada; Contractor, General Dynamics Information Technology, Falls Church, VA, USA; Centre of Excellence on Post-Traumatic Stress Disorder, Ottawa, ON, Canada.
Brain Cogn. 2021 Nov;154:105790. doi: 10.1016/j.bandc.2021.105790. Epub 2021 Sep 3.
The purpose of this study was to examine the association between the apolipoprotein E (APOE) ε4 allele and neurocognitive functioning following traumatic brain injury (TBI) in military service members and veterans (SMVs). Participants included 176 SMVs with a history of remote TBI (≥1 year post-injury), categorized into mild (n = 100), moderate (n = 40), and severe (n = 36) TBI groups. Participants completed a neuropsychological assessment and APOE genotyping (n = 46 ε4+, n = 130 ε4-). Neurocognitive composite scores representing memory, executive functioning, and visual processing speed were computed. ANCOVAs adjusting for race, education, combat exposure, and PTSD symptom severity showed a significant main effect of ε4 on the memory composite, such that ε4+ SMVs exhibited poorer memory performance than ε4- SMVs. When ε2 allele carriers were removed from the analyses, associations with memory were strengthened, demonstrating a possible protective effect of the ε2 allele. No main effect of TBI group was identified on any cognitive composite, nor were there any significant TBI group × ε4 status interactions for any cognitive composite. Future studies with larger samples are needed to verify these findings, but our results suggest an important relationship between ε4 status and memory functioning following remote TBI of all severities.
这项研究的目的是探讨载脂蛋白 E (APOE) ε4 等位基因与军事人员和退伍军人(SMV)创伤性脑损伤(TBI)后神经认知功能的关系。参与者包括 176 名有远程 TBI 病史的 SMV(≥受伤后 1 年),分为轻度(n=100)、中度(n=40)和重度(n=36)TBI 组。参与者完成了神经心理学评估和 APOE 基因分型(n=46 ε4+,n=130 ε4-)。计算了代表记忆、执行功能和视觉处理速度的神经认知综合评分。调整种族、教育、战斗暴露和 PTSD 症状严重程度的 ANCOVA 显示,ε4 对记忆综合有显著的主效应,即 ε4+SMV 的记忆表现比 ε4-SMV 差。当从分析中去除 ε2 等位基因携带者时,与记忆的关联得到了加强,表明 ε2 等位基因可能具有保护作用。在任何认知综合中,TBI 组均无主要影响,也没有任何认知综合的 TBI 组×ε4 状态交互作用。需要更大样本的未来研究来验证这些发现,但我们的结果表明,ε4 状态与所有严重程度的远程 TBI 后记忆功能之间存在重要关系。