Tripodis Yorghos, Alosco Michael L, Zirogiannis Nikolaos, Gavett Brandon E, Chaisson Christine, Martin Brett, McClean Michael D, Mez Jesse, Kowall Neil, Stern Robert A
Boston University School of Public Health, Boston, MA, USA.
Alzheimer's Disease Center, Boston University School of Medicine, Boston, MA, USA.
J Alzheimers Dis. 2017;59(1):251-263. doi: 10.3233/JAD-160585.
Traumatic brain injury (TBI) is thought to be a risk factor for dementia, including dementia due to Alzheimer's disease (AD). However, the influence of TBI history on the neuropsychological course of AD is unknown and, more broadly, the effect of TBI history on age-related cognitive change is poorly understood. We examined the relationship between history of TBI with loss of consciousness (LOC) history and cognitive change in participants with normal cognition and probable AD, stratified by APOEɛ4 allele status. The sample included 706 participants (432 with normal cognition; 274 probable AD) from the National Alzheimer's Coordinating Center (NACC) dataset that completed the Uniform Data Set evaluation between 2005 and 2014. Normal and probable AD participants with a history of TBI were matched to an equal number of demographically and clinically similar participants without a TBI history. In this dataset, TBI with LOC was defined as brain trauma with brief or extended unconsciousness. For the normal and probable AD cohorts, there was an average of 3.2±1.9 and 1.8±1.1 years of follow-up, respectively. 30.8% of the normal cohort were APOEɛ4 carriers, whereas 70.8% of probable AD participants were carriers. Mixed effects regressions showed TBI with LOC history did not affect rates of cognitive change in APOEɛ4 carriers and non-carriers. Findings from this study suggest that TBI with LOC may not alter the course of cognitive function in older adults with and without probable AD. Future studies that better characterize TBI (e.g., severity, number of TBIs, history of subconconcussive exposure) are needed to clarify the association between TBI and long-term neurocognitive outcomes.
创伤性脑损伤(TBI)被认为是痴呆症的一个风险因素,包括阿尔茨海默病(AD)所致的痴呆症。然而,TBI病史对AD神经心理学病程的影响尚不清楚,更广泛地说,TBI病史对与年龄相关的认知变化的影响也知之甚少。我们研究了有失去意识(LOC)病史的TBI病史与认知正常和可能患有AD的参与者的认知变化之间的关系,并根据APOEɛ4等位基因状态进行分层。样本包括来自国家阿尔茨海默病协调中心(NACC)数据集的706名参与者(432名认知正常者;274名可能患有AD者),他们在2005年至2014年期间完成了统一数据集评估。有TBI病史的认知正常和可能患有AD的参与者与同等数量的在人口统计学和临床上相似但无TBI病史的参与者进行匹配。在这个数据集中,伴有LOC的TBI被定义为伴有短暂或长期无意识的脑外伤。对于认知正常和可能患有AD的队列,随访时间平均分别为3.2±1.9年和1.8±1.1年。认知正常队列中30.8%是APOEɛ4携带者,而可能患有AD的参与者中有70.8%是携带者。混合效应回归显示,伴有LOC病史的TBI不会影响APOEɛ4携带者和非携带者的认知变化率。这项研究的结果表明,伴有LOC的TBI可能不会改变患有或未患有可能AD的老年人的认知功能进程。需要进一步开展研究,更好地描述TBI的特征(如严重程度、TBI的次数、亚脑震荡暴露史),以阐明TBI与长期神经认知结果之间的关联。