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影响阿尔茨海默病和相关痴呆症的韧性和预防的因素。

Factors Affecting Resilience and Prevention of Alzheimer's Disease and Related Dementias.

机构信息

Department of Neurology, New York University Grossman School of Medicine, New York, NY, USA.

Center for Cognitive Neurology, New York University Grossman School of Medicine, New York, NY, USA.

出版信息

Ann Neurol. 2024 Oct;96(4):633-649. doi: 10.1002/ana.27055. Epub 2024 Aug 17.

Abstract

Alzheimer's disease (AD) is a devastating, age-associated neurodegenerative disorder and the most common cause of dementia. The clinical continuum of AD spans from preclinical disease to subjective cognitive decline, mild cognitive impairment, and dementia stages (mild, moderate, and severe). Neuropathologically, AD is defined by the accumulation of amyloid β (Aβ) into extracellular plaques in the brain parenchyma and in the cerebral vasculature, and by abnormally phosphorylated tau that accumulates intraneuronally forming neurofibrillary tangles (NFTs). Development of treatment approaches that prevent or even reduce the cognitive decline because of AD has been slow compared to other major causes of death. Recently, the United States Food and Drug Administration gave full approval to 2 different Aβ-targeting monoclonal antibodies. However, this breakthrough disease modifying approach only applies to a limited subset of patients in the AD continuum and there are stringent eligibility criteria. Furthermore, these approaches do not prevent progression of disease, because other AD-related pathologies, such as NFTs, are not directly targeted. A non-mutually exclusive alternative is to address lifestyle interventions that can help reduce the risk of AD and AD-related dementias (ADRD). It is estimated that addressing such modifiable risk factors could potentially delay up to 40% of AD/ADRD cases. In this review, we discuss some of the many modifiable risk factors that may be associated with prevention of AD/ADRD and/or increasing brain resilience, as well as other factors that may interact with these modifiable risk factors to influence AD/ADRD progression. [Color figure can be viewed at www.annalsofneurology.org] ANN NEUROL 2024;96:633-649.

摘要

阿尔茨海默病(AD)是一种破坏性的、与年龄相关的神经退行性疾病,也是痴呆症最常见的原因。AD 的临床连续体从临床前疾病跨越到主观认知下降、轻度认知障碍和痴呆阶段(轻度、中度和重度)。从神经病理学角度来看,AD 定义为淀粉样蛋白β(Aβ)在脑实质和脑血管中积累形成细胞外斑块,以及异常磷酸化的 tau 在神经元内积累形成神经原纤维缠结(NFTs)。与其他主要死因相比,开发预防甚至减缓 AD 导致认知能力下降的治疗方法进展缓慢。最近,美国食品和药物管理局(FDA)全面批准了 2 种不同的 Aβ靶向单克隆抗体。然而,这种突破性的疾病修饰方法仅适用于 AD 连续体中的有限亚组患者,并且有严格的资格标准。此外,这些方法并不能阻止疾病的进展,因为 NFT 等其他与 AD 相关的病理变化并没有被直接靶向。一个非互斥的替代方案是采用生活方式干预措施,这有助于降低 AD 和 AD 相关痴呆(ADRD)的风险。据估计,解决这些可改变的风险因素可能会使 AD/ADRD 病例的发生延迟高达 40%。在这篇综述中,我们讨论了一些可能与 AD/ADRD 预防和/或增加大脑弹性相关的许多可改变的风险因素,以及可能与这些可改变的风险因素相互作用影响 AD/ADRD 进展的其他因素。[彩色图片可在 annalsofneurology.org 查看]ANN NEUROL 2024;96:633-649.

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