Gardner Raquel C, Burke James F, Nettiksimmons Jasmine, Kaup Allison, Barnes Deborah E, Yaffe Kristine
Memory and Aging Center, Department of Neurology, University of California, San Francisco2Department of Veterans Affairs, San Francisco Veterans Affairs Medical Center, San Francisco, California.
Department of Neurology, University of Michigan, Ann Arbor4Department of Veterans Affairs, Veterans Affairs Center for Clinical Management and Research, Ann Arbor Veterans Affairs Healthcare System, Ann Arbor, Michigan.
JAMA Neurol. 2014 Dec;71(12):1490-7. doi: 10.1001/jamaneurol.2014.2668.
Epidemiologic evidence regarding the importance of traumatic brain injury (TBI) as a risk factor for dementia is conflicting. Few previous studies have used patients with non-TBI trauma (NTT) as controls to investigate the influence of age and TBI severity.
To quantify the risk of dementia among adults with recent TBI compared with adults with NTT.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study was performed from January 1, 2005, through December 31, 2011 (follow-up, 5-7 years). All patients 55 years or older diagnosed as having TBI or NTT in 2005 and 2006 and who did not have baseline dementia or die during hospitalization (n = 164,661) were identified in a California statewide administrative health database of emergency department (ED) and inpatient visits.
Mild vs moderate to severe TBI diagnosed by Centers for Disease Control and Prevention criteria using International Classification of Diseases, Ninth Revision (ICD-9)codes, and NTT, defined as fractures excluding fractures of the head and neck, diagnosed using ICD-9 codes.
Incident ED or inpatient diagnosis of dementia (using ICD-9 codes) 1 year or more after initial TBI or NTT. The association between TBI and risk of dementia was estimated using Cox proportional hazards models before and after adjusting for common dementia predictors and potential confounders. We also stratified by TBI severity and age category (55-64, 65-74, 75-84, and ≥85 years).
A total of 51,799 patients with trauma (31.5%) had TBI. Of these, 4361 (8.4%) developed dementia compared with 6610 patients with NTT (5.9%) (P < .001). We found that TBI was associated with increased dementia risk (hazard ratio [HR], 1.46; 95% CI, 1.41-1.52; P < .001). Adjustment for covariates had little effect except adjustment for age category (fully adjusted model HR, 1.26; 95% CI, 1.21-1.32; P < .001). In stratified adjusted analyses, moderate to severe TBI was associated with increased risk of dementia across all ages (age 55-64: HR, 1.72; 95% CI, 1.40-2.10; P < .001; vs age 65-74: HR, 1.46; 95% CI, 1.30-1.64; P < .001), whereas mild TBI may be a more important risk factor with increasing age (age 55-64: HR, 1.11; 95% CI, 0.80-1.53; P = .55; vs age 65-74: HR, 1.25; 95% CI, 1.04-1.51; P = .02; age interaction P < .001).
Among patients evaluated in the ED or inpatient settings, those with moderate to severe TBI at 55 years or older or mild TBI at 65 years or older had an increased risk of developing dementia. Younger adults may be more resilient to the effects of recent mild TBI than older adults.
关于创伤性脑损伤(TBI)作为痴呆症风险因素的重要性,流行病学证据存在冲突。以前很少有研究将非TBI创伤(NTT)患者作为对照,以调查年龄和TBI严重程度的影响。
量化近期发生TBI的成年人与NTT成年人相比患痴呆症的风险。
设计、设置和参与者:这项回顾性队列研究于2005年1月1日至2011年12月31日进行(随访5至7年)。在加利福尼亚州全州范围内的急诊部(ED)和住院就诊行政健康数据库中,识别出所有在2005年和2006年被诊断为患有TBI或NTT且年龄在55岁及以上、住院期间没有基线痴呆症或死亡的患者(n = 164,661)。
根据疾病控制和预防中心的标准,使用国际疾病分类第九版(ICD-9)编码诊断的轻度与中度至重度TBI,以及NTT,定义为排除头颈部骨折的骨折,使用ICD-9编码诊断。
初次TBI或NTT后1年或更长时间发生的ED或住院痴呆症诊断(使用ICD-9编码)。在调整常见的痴呆症预测因素和潜在混杂因素之前和之后,使用Cox比例风险模型估计TBI与痴呆症风险之间的关联。我们还按TBI严重程度和年龄类别(55 - 64岁、65 - 74岁、75 - 84岁和≥85岁)进行分层。
共有51,799名创伤患者(31.5%)患有TBI。其中,4361名(8.4%)患痴呆症,而NTT患者中有6610名(5.9%)患痴呆症(P <.001)。我们发现TBI与痴呆症风险增加相关(风险比[HR],1.46;95%置信区间,1.41 - 1.52;P <.001)。除了按年龄类别进行调整外,对协变量的调整影响不大(完全调整模型HR,1.26;95%置信区间,1.21 - 1.32;P <.001)。在分层调整分析中,中度至重度TBI在所有年龄段都与痴呆症风险增加相关(55 - 64岁:HR,1.72;95%置信区间,1.40 - 2.10;P <.001;与65 - 74岁相比:HR,1.46;95%置信区间,1.30 - 1.64;P <.001),而轻度TBI可能随着年龄增长成为更重要的风险因素(55 - 64岁:HR,1.11;95%置信区间,0.80 - 1.53;P =.55;与65 - 74岁相比:HR,1.25;95%置信区间,1.04 - 1.51;P =.02;年龄交互作用P <.001)。
在ED或住院环境中接受评估的患者中,55岁及以上患有中度至重度TBI或65岁及以上患有轻度TBI的患者患痴呆症的风险增加。年轻成年人可能比老年人对近期轻度TBI的影响更具弹性。