Psychiatry and Behavioral Medicine, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Alzheimer's Disease Research Center, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Biomolecules. 2024 Feb 24;14(3):274. doi: 10.3390/biom14030274.
Alzheimer's disease (AD) is a neurodegenerative disorder affecting nearly one in nine older adults in the US. This number is expected to grow exponentially, thereby increasing stress on caregivers and health systems. While some risk factors for developing AD are genetic, an estimated 1/3 of AD cases are attributed to lifestyle. Many of these risk factors emerge decades before clinical symptoms of AD are detected, and targeting them may offer more efficacious strategies for slowing or preventing disease progression. This review will focus on two common risk factors for AD, metabolic dysfunction and sleep impairments, and discuss potential mechanisms underlying their relationship to AD pathophysiology. Both sleep and metabolism can alter AD-related protein production and clearance, contributing to an imbalance that drives AD progression. Additionally, these risk factors have bidirectional relationships with AD, where the presence of AD-related pathology can further disrupt sleep and worsen metabolic functioning. Sleep and metabolism also appear to have a bidirectional relationship with each other, indirectly exacerbating AD pathophysiology. Understanding the mechanisms involved in these relationships is critical for identifying new strategies to slow the AD cascade.
阿尔茨海默病(AD)是一种神经退行性疾病,影响美国近九分之一的老年人。预计这一数字将呈指数级增长,从而增加护理人员和医疗系统的压力。虽然 AD 的一些风险因素是遗传的,但据估计,1/3 的 AD 病例归因于生活方式。这些风险因素中的许多在 AD 的临床症状出现之前几十年就出现了,针对这些因素可能为减缓或预防疾病进展提供更有效的策略。这篇综述将重点关注 AD 的两个常见风险因素,即代谢功能障碍和睡眠障碍,并讨论它们与 AD 病理生理学之间关系的潜在机制。睡眠和代谢都可以改变与 AD 相关的蛋白质产生和清除,导致失衡,从而推动 AD 进展。此外,这些风险因素与 AD 之间存在双向关系,AD 相关病理的存在会进一步破坏睡眠并恶化代谢功能。睡眠和代谢之间似乎也存在相互关系,间接加重 AD 的病理生理学。了解这些关系中涉及的机制对于确定减缓 AD 级联反应的新策略至关重要。