4.5 Article

Prevalence of Traumatic Brain Injury in Early Versus Late-Onset Alzheimer's Disease

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 47, 期 4, 页码 985-993

出版社

IOS PRESS
DOI: 10.3233/JAD-143207

关键词

Aging; Alzheimer's disease; concussion; dementia; epidemiology; head injury; memory loss; neurodegeneration; risk factors; traumatic brain injury

资金

  1. Medical Student Training in Aging Research Program, the National Institute on Aging [T35AG026736]
  2. John A. Hartford Foundation
  3. Lillian R. Gleitsman Foundation
  4. NIA [U01 AG016976, P30 AG019610, P30 AG013846, P50 AG008702, P50 AG025688, P30 AG010133, P50 AG005146, P50 AG005134, P50 AG016574, P50 AG005138, P30 AG008051, P30 AG013854, P30 AG008017]
  5. NIA/NIH [U01 AG016976]
  6. The NIA [P30 AG010161, P30 AG010129, P50 AG016573, P50 AG016570, P50 AG005131, P50 AG023501, P30 AG035982, P30 AG028383, P30 AG010124, P50 AG005133, P50 AG005142, P30 AG012300, P50 AG005136, P50 AG033514, P50 AG005681]
  7. NATIONAL CENTER FOR RESEARCH RESOURCES [P41RR013642] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE ON AGING [P50AG008702, P50AG005681, P30AG013846, P30AG008017, P30AG012300, P30AG010129, P50AG005138, P50AG025688, P50AG005142, U01AG016976, P30AG010133, R01AG034499, P50AG005131, P50AG016573, P50AG033514, P50AG005133, P50AG005134, P30AG010161, P50AG005146, P50AG016570, T35AG026736, P30AG013854, P30AG035982, P30AG010124, P30AG008051, P30AG019610, P50AG005136, P50AG016574, P30AG028383, P50AG023501] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Background: Traumatic brain injury (TBI) is the most established environmental risk factor for Alzheimer's disease (AD), but it is unclear if TBI is specifically associated with early-onset AD (EOAD). Objective: To evaluate the relationship between TBI and EOAD (<65 years). Methods: We identified 1,449 EOAD, 4,337 late-onset AD (LOAD), and corresponding EOAD-matched and LOAD-matched normal controls (NC) in the National Alzheimer's Coordinating Center Uniform (NACC) database and compared the prevalence of any history of TBI as well as measures of cognition, function, behavior, and neuropathology. For validation, we determined TBI prevalence among 115 well-characterized clinic patients with EOAD. Results: Part A: The prevalence of any TBI in the NACC-database EOAD participants (13.3%) was comparable to that observed in the clinic EOAD patients (13.9%) but significantly higher than in the NACC-database LOAD participants (7.7%; p < 0.0001) and trended to higher compared to EOAD-matched NC (11.1%; logistic regression p = 0.053). Part B: When we compared EOAD patients with documented non-acute and non-residually impairing TBI to EOAD without a documented history of prior TBI, those with TBI had significantly more disinhibition. Part C: Autopsies did not reveal differences in AD neuropathology based on a history of TBI. Conclusions: These findings suggest, but do not establish, that TBI is a specific risk factor for EOAD and may lead to disinhibition, a feature that often results from the frontal effects of head injury. This study recommends further research on the effects of TBI in EOAD in larger numbers of participants.

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