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创伤性脑损伤与长期脑改变、病理性标志物蓄积及痴呆发生风险:综述

Traumatic Brain Injury and Risk of Long-Term Brain Changes, Accumulation of Pathological Markers, and Developing Dementia: A Review.

机构信息

Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Department of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

J Alzheimers Dis. 2019;70(3):629-654. doi: 10.3233/JAD-190028.

Abstract

Traumatic brain injuries (TBI) have received widespread media attention in recent years as being a risk factor for the development of dementia and chronic traumatic encephalopathy (CTE). This has sparked fears about the potential long-term effects of TBI of any severity on cognitive aging, leading to a public health concern. This article reviews the evidence surrounding TBI as a risk factor for the later development of changes in brain structure and function, and an increased risk of neurodegenerative disorders. A number of studies have shown evidence of long-term brain changes and accumulation of pathological biomarkers (e.g., amyloid and tau proteins) related to a history of moderate-to-severe TBI, and research has also demonstrated that individuals with moderate-to-severe injuries have an increased risk of dementia. While milder injuries have been found to be associated with an increased risk for dementia in some recent studies, reports on long-term brain changes have been mixed and often are complicated by factors related to injury exposure (i.e., number of injuries) and severity/complications, psychiatric conditions, and opioid use disorder. CTE, although often described as a neurodegenerative disorder, remains a neuropathological condition that is poorly understood. Future research is needed to clarify the significance of CTE pathology and determine whether that can explain any clinical symptoms. Overall, it is clear that most individuals who sustain a TBI (particularly milder injuries) do not experience worse outcomes with aging, as the incidence for dementia is found to be less than 7% across the literature.

摘要

创伤性脑损伤 (TBI) 近年来受到广泛关注,因为它是痴呆症和慢性创伤性脑病 (CTE) 发展的一个风险因素。这引发了人们对任何严重程度的 TBI 对认知老化的潜在长期影响的担忧,导致了公众健康问题。本文综述了 TBI 作为脑结构和功能改变以及神经退行性疾病风险增加的危险因素的证据。许多研究表明,有证据表明长期的脑变化和与中度至重度 TBI 相关的病理生物标志物(例如淀粉样蛋白和tau 蛋白)的积累,研究还表明,中度至重度损伤的个体痴呆的风险增加。虽然一些最近的研究发现轻度损伤与痴呆风险增加有关,但关于长期脑变化的报告喜忧参半,而且往往因与损伤暴露(即损伤次数)和严重程度/并发症、精神状况和阿片类药物使用障碍相关的因素而变得复杂。CTE 虽然通常被描述为神经退行性疾病,但仍然是一种神经病理学状况,尚未得到充分理解。需要进一步的研究来阐明 CTE 病理学的意义,并确定它是否可以解释任何临床症状。总的来说,很明显,大多数遭受 TBI 的人(尤其是轻度损伤)在衰老过程中不会出现更糟糕的结果,因为文献中痴呆的发病率低于 7%。

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