Department of Psychiatry, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Departments of Psychiatry and Neurological Surgery, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Arch Clin Neuropsychol. 2024 Apr 24;39(3):325-334. doi: 10.1093/arclin/acae003.
Evaluate whether traumatic brain injury (TBI) characteristics, age of injury, or recency of injury predicts the course of neurocognitive decline and/or increases conversion rates to mild cognitive impairment (MCI) or dementia.
Data were obtained from the National Alzheimer's Coordinating Center for participants 50-85 years old with 3-5 visits from 2015 to 2022, with or without TBI history (TBI+ = 508; TBI- = 2,382). Groups were stratified by self-reported TBI history (i.e., single TBI without loss of consciousness [LOC], single TBI with LOC, multiple TBI without LOC, and multiple TBI with LOC), age of most recent TBI, and recency of TBI. Mixed linear models compared neuropsychological composite trajectories (executive functioning/attention/speed, language, memory, and global), co-varying for age, gender, education, apolipoprotein E4 status, race/ethnicity, and baseline diagnosis (normal aging n = 1,720, MCI n = 749, or dementia n = 417). Logistic binary regression examined MCI/dementia conversion rates.
There was a slightly higher frequency of MCI/dementia in those with multiple TBIs (50% to 60% with and without LOC, compared to 39% with no TBI) at baseline, but longitudinal trajectories were similar. TBI history, age of injury, or recency of injury did not impact neurocognitive trajectories or conversion rates to MCI/dementia (all p's > .01).
TBI history, regardless of injury characteristics, age of injury, or recency of injury, did not worsen neurocognitive decline or MCI/dementia conversion. Additional longitudinal research in more diverse cohorts with a wider range of TBI severity is needed to evaluate the specific factors and possible mechanisms in which TBI may increase dementia risk.
评估创伤性脑损伤 (TBI) 特征、受伤年龄或受伤时间的新近程度是否预测神经认知能力下降的进程和/或增加向轻度认知障碍 (MCI) 或痴呆的转化率。
数据来自国家阿尔茨海默病协调中心,参与者年龄在 50-85 岁之间,2015 年至 2022 年期间有 3-5 次就诊,有或没有 TBI 病史(TBI+ = 508;TBI-= 2382)。根据自我报告的 TBI 病史(即无意识单次 TBI、有意识单次 TBI、无意识多次 TBI 和有意识多次 TBI)、最近一次 TBI 的年龄和 TBI 的新近程度对各组进行分层。混合线性模型比较了神经心理学综合轨迹(执行功能/注意力/速度、语言、记忆和整体),同时考虑了年龄、性别、教育、载脂蛋白 E4 状态、种族/民族和基线诊断(正常老化 n=1720、MCI n=749 或痴呆 n=417)。逻辑二元回归分析了 MCI/痴呆的转化率。
基线时,有无意识 TBI 的多次 TBI 患者(50%至 60%)的 MCI/痴呆发生率略高(而无 TBI 者为 39%),但纵向轨迹相似。TBI 病史、受伤年龄或受伤时间的新近程度均不影响神经认知轨迹或向 MCI/痴呆的转化率(所有 p 值均>0.01)。
TBI 病史无论损伤特征、受伤年龄或受伤时间的新近程度如何,均不会加重神经认知衰退或 MCI/痴呆的转化率。需要在更多样化的队列中进行更多的纵向研究,以评估 TBI 可能增加痴呆风险的具体因素和可能机制,这些队列具有更广泛的 TBI 严重程度范围。