Sun Bryan, Li Lulin, Harris Odette A, Luo Jian
Palo Alto Veterans Institute for Research, VA Palo Alto Health Care System, Palo Alto, CA, 94304, USA.
Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Transl Neurodegener. 2025 Mar 26;14(1):16. doi: 10.1186/s40035-025-00478-5.
Traumatic brain injury (TBI) has emerged as a significant risk factor for Alzheimer's disease (AD), a complex and devastating neurodegenerative disorder characterized by progressive cognitive decline and memory loss. Both conditions share a common feature: blood‒brain barrier (BBB) dysfunction, which is believed to play a pivotal role in linking TBI to the development of AD. This review delves into the intricate relationship between TBI and AD, with a focus on BBB dysfunction and its critical role in disease mechanisms and therapeutic development. We first present recent evidence from epidemiological studies highlighting the increased incidence of AD among individuals with a history of TBI, as well as pathological and animal model studies that demonstrate how TBI can accelerate AD-like pathology. Next, we explore the mechanisms by which BBB dysfunction may mediate TBI-induced AD pathology. Finally, we investigate the shared molecular pathways associated with BBB dysfunction in both TBI and AD conditions and discuss the latest findings on how targeting these pathways and employing regenerative approaches, such as stem cell therapy and pharmacological interventions, can enhance BBB function and mitigate neurodegeneration.
创伤性脑损伤(TBI)已成为阿尔茨海默病(AD)的一个重要风险因素,AD是一种复杂且具有破坏性的神经退行性疾病,其特征为进行性认知衰退和记忆丧失。这两种病症有一个共同特征:血脑屏障(BBB)功能障碍,据信这在将TBI与AD的发展联系起来方面起着关键作用。本综述深入探讨了TBI与AD之间的复杂关系,重点关注BBB功能障碍及其在疾病机制和治疗发展中的关键作用。我们首先展示了流行病学研究的最新证据,这些证据突出了有TBI病史的个体中AD发病率的增加,以及病理和动物模型研究,这些研究证明了TBI如何加速类似AD的病理过程。接下来,我们探讨BBB功能障碍可能介导TBI诱导的AD病理的机制。最后,我们研究了TBI和AD情况下与BBB功能障碍相关的共同分子途径,并讨论了关于如何靶向这些途径以及采用再生方法(如干细胞疗法和药物干预)来增强BBB功能和减轻神经退行性变的最新发现。