Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, State Key Laboratory of Trauma and Chemical Poisoning, Third Military Medical University, Chongqing, China.
Chongqing Key Laboratory of Ageing and Brain Diseases, Chongqing, China.
Alzheimers Dement. 2024 Aug;20(8):5720-5739. doi: 10.1002/alz.13864. Epub 2024 Jun 2.
Alzheimer's disease (AD) is a neurodegenerative disease that involves multiple systems in the body. Numerous recent studies have revealed bidirectional crosstalk between the brain and bone, but the interaction between bone and brain in AD remains unclear. In this review, we summarize human studies of the association between bone and brain and provide an overview of their interactions and the underlying mechanisms in AD. We review the effects of AD on bone from the aspects of AD pathogenic proteins, AD risk genes, neurohormones, neuropeptides, neurotransmitters, brain-derived extracellular vesicles (EVs), and the autonomic nervous system. Correspondingly, we elucidate the underlying mechanisms of the involvement of bone in the pathogenesis of AD, including bone-derived hormones, bone marrow-derived cells, bone-derived EVs, and inflammation. On the basis of the crosstalk between bone and the brain, we propose potential strategies for the management of AD with the hope of offering novel perspectives on its prevention and treatment. HIGHLIGHTS: The pathogenesis of AD, along with its consequent changes in the brain, may involve disturbing bone homeostasis. Degenerative bone disorders may influence the progression of AD through a series of pathophysiological mechanisms. Therefore, relevant bone intervention strategies may be beneficial for the comprehensive management of AD.
阿尔茨海默病(AD)是一种涉及体内多个系统的神经退行性疾病。最近的大量研究揭示了大脑和骨骼之间的双向串扰,但 AD 中骨骼和大脑之间的相互作用尚不清楚。在这篇综述中,我们总结了人类对骨骼和大脑之间关联的研究,并概述了它们在 AD 中的相互作用和潜在机制。我们从 AD 致病蛋白、AD 风险基因、神经激素、神经肽、神经递质、脑源性细胞外囊泡(EV)和自主神经系统等方面综述了 AD 对骨骼的影响。相应地,我们阐明了骨骼参与 AD 发病机制的潜在机制,包括骨骼衍生的激素、骨髓衍生的细胞、骨骼衍生的 EV 和炎症。基于骨骼和大脑之间的串扰,我们提出了 AD 管理的潜在策略,希望为 AD 的预防和治疗提供新的视角。重点:AD 的发病机制以及随之而来的大脑变化,可能涉及扰乱骨骼内稳态。退行性骨病可能通过一系列病理生理机制影响 AD 的进展。因此,相关的骨骼干预策略可能有助于 AD 的综合管理。