Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Department of Hepatology & Gastroenterology, Division of Surgery and Cancer, Imperial College London, St Mary's Campus, UK.
J Alzheimers Dis. 2020;75(1):1-14. doi: 10.3233/JAD-190848.
Clinical specialization is not only a force for progress, but it has also led to the fragmentation of medical knowledge. The focus of research in the field of Alzheimer's disease (AD) is neurobiology, while hepatologists focus on liver diseases and lipid specialists on atherosclerosis. This article on AD focuses on the role of the liver and lipid homeostasis in the development of AD. Amyloid-β (Aβ) deposits accumulate as plaques in the brain of an AD patient long before cognitive decline is evident. Aβ generation is a normal physiological process; the steady-state level of Aβ in the brain is determined by balance between Aβ production and its clearance. We present evidence suggesting that the liver is the origin of brain Aβ deposits and that it is involved in peripheral clearance of circulating Aβ in the blood. Hence the liver could be targeted to decrease Aβ production or increase peripheral clearance.
临床专业化不仅是进步的动力,而且导致了医学知识的碎片化。阿尔茨海默病(AD)领域的研究重点是神经生物学,而肝病学家关注肝脏疾病,脂质专家关注动脉粥样硬化。这篇关于 AD 的文章重点介绍了肝脏和脂质动态平衡在 AD 发展中的作用。在认知能力下降明显之前,AD 患者大脑中的淀粉样蛋白-β(Aβ)沉积物就已经以斑块的形式积累。Aβ 的产生是一个正常的生理过程;大脑中 Aβ 的稳态水平取决于 Aβ 产生和清除之间的平衡。我们提出的证据表明,肝脏是大脑 Aβ 沉积物的起源,并且它参与了血液中循环 Aβ 的外周清除。因此,肝脏可以作为靶点来减少 Aβ 的产生或增加外周清除。