解锁阿尔茨海默病的未来:诊断和治疗的创新。

Q3 Medicine
Man Mohan Mehndiratta, Monika Singla, Abhishek Dixit
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引用次数: 0

摘要

阿尔茨海默病(AD)是最常见的痴呆症之一,约占全球所有痴呆症病例的三分之二。尽管发病率很高,但估计仍有4100万痴呆症患者未得到诊断,只有约25%的痴呆症患者得到临床确诊。阿尔茨海默病是导致痴呆的主要神经退行性疾病,其特征是神经元萎缩和丧失。毒性β淀粉样蛋白(Aβ)寡聚物、蛋白聚集体的积累,以及神经元内神经原纤维缠结(nft)的形成,是AD的关键病理特征。nft由过度磷酸化的tau蛋白组成。这些异常导致脑内葡萄糖代谢下降、突触功能障碍和线粒体损伤。AD的进展分为三个阶段:(1)症状前阶段,(2)轻度认知障碍(MCI)阶段,(3)AD临床阶段。许多生物标志物已被确定用于诊断阿尔茨海默病并与非典型阿尔茨海默病区分。它已经成为一个关键的研究领域,为阿尔茨海默病的早期发现、预测以及计划药物治疗和监测提供了巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unlocking the Future of Alzheimer's Disease: Innovations in Diagnosis and Therapy.

Alzheimer's disease (AD) is one of the most common forms of dementia, making up around two thirds of all dementia cases globally. Despite its high prevalence, it is estimated to remain undiagnosed in 41 million people with dementia, and with only about 25% of dementia individuals being clinically identified. AD is the major neurodegenerative disorder leading to dementia, characterized by neuronal atrophy and loss. The accumulation of toxic amyloid-beta (Aβ) oligomers, protein aggregates, along with the formation of neurofibrillary tangles (NFTs) within neurons, is the key pathological feature of AD. NFTs are composed of hyperphosphorylated tau protein. These abnormalities contribute to a decline in cerebral glucose metabolism in the brain, synaptic dysfunction, and mitochondrial impairment. The progression of AD occurs in three stages: (1) the presymptomatic stage, (2) mild cognitive impairment (MCI), and (3) the clinical stage of AD. Many biomarkers have been identified for diagnosing AD and differentiating it from atypical AD. It has emerged as a key area of research, offering significant potential for early detection of AD, prognostication, as well as planning drug therapy and monitoring.

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