阿尔茨海默病研究的突破:通往更有希望的未来之路?

IF 1.8 Q4 NEUROSCIENCES Annals of Neurosciences Pub Date : 2024-01-01 Epub Date: 2023-08-21 DOI:10.1177/09727531231187235
Hareer Fatima, Hussain Sohail Rangwala, Faiza Riaz, Burhanuddin Sohail Rangwala, Mohammad Arham Siddiq
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种广泛存在的神经退行性疾病,具有重大的全球影响,影响约5000万人,预计到2050年,将有多达1.52亿人受到影响。AD的特征是大脑中的β淀粉样蛋白斑块和tau缠结,导致认知能力下降。最近对AD的研究取得了重大进展,包括开发了一种“淀粉样蛋白时钟”生物标志物,通过正电子发射断层扫描(PET)跟踪AD的进展。Surf4和其他基因已被发现在调节β淀粉样蛋白毒性中发挥作用,而抑制己糖激酶-2在临床前研究中显示出积极的结果。新的大脑绘图技术已经确定了AD认知变化的早期大脑原因,神经元五肽蛋白Nptx2和烟碱乙酰胆碱受体的星形细胞7亚基(7nAChRs)等生物标志物显示出早期检测的潜力。其他方法,如补充酶Tip60,用PRZ-18002选择性降解修饰蛋白p-p38,以及靶向蛋白电压依赖性阴离子通道-1(VDAC1),已显示出在增强认知功能和预防与AD相关的病理生理学改变方面的前景,和胶质纤维酸性蛋白(GFAP)也被发现用于AD的早期检测和干预。此外,最近美国食品药品监督管理局批准了aducanumab和lecanemab等药物,为减少AD症状和改善功能提供了选择,而痴呆症疫苗的临床试验显示,鼻腔和β-淀粉样蛋白40疫苗以及针对tau的疫苗有前景。AD研究的这些进展,包括生物标志物的发现和疾病改良治疗的开发,是改善AD患者生活和找到治疗这种衰弱疾病的方法的关键步骤。
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Breakthroughs in Alzheimer's Research: A Path to a More Promising Future?

Background: Alzheimer's disease (AD) is a widespread neurodegenerative disorder with a significant global impact, affecting approximately 50 million individuals, and projections estimate that up to 152 million people will be affected by 2050. AD is characterized by beta-amyloid plaques and tau tangles in the brain, leading to cognitive decline.

Summary: Recent research on AD has made significant strides, including the development of an "amyloid clock" biomarker that tracks AD progression through positron emission tomography (PET) scans. Surf4 and other genes have been discovered to play a role in regulating beta-amyloid toxicity, while inhibiting the enzyme hexokinase-2 has shown positive results in preclinical studies. New brain mapping techniques have identified early brain-based causes of cognitive changes in AD, and biomarkers such as neuronal pentraxin protein Nptx2 and astrocytic 7-subunit of the nicotinic acetylcholine receptors (7nAChRs) show potential for early detection. Other approaches, such as replenishing the enzyme Tip60, selectively degrading the modified protein p-p38 with PRZ-18002, and targeting the protein voltage-dependent anion channel-1 (VDAC1), have shown promise in enhancing cognitive function and preventing pathophysiological alterations linked to AD. Baseline blood samples and other biomarkers such as urine formic acid, p-tau 198, microRNAs, and glial fibrillary acidic protein (GFAP) have also been discovered for early detection and intervention of AD. Additionally, recent FDA approvals for medications such as aducanumab and lecanemab provide options for reducing AD symptoms and improving function, while clinical trials for dementia vaccines show promise for the nasal and beta-amyloid 40 vaccines as well as vaccinations targeting tau.

Key messages: These advancements in AD research, including biomarker discovery and the development of disease-modifying treatments, are crucial steps towards improving the lives of those affected by AD and finding a cure for this debilitating disease.

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来源期刊
Annals of Neurosciences
Annals of Neurosciences NEUROSCIENCES-
CiteScore
2.40
自引率
0.00%
发文量
39
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