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Alzheimer's disease

机译:阿尔茨海默氏病

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In this Seminar, we highlight the main developments in the field of Alzheimer's disease. The most recent data indicate that, by 2050, the prevalence of dementia will double in Europe and triple worldwide, and that estimate is 3 times higher when based on a biological (rather than clinical) definition of Alzheimer's disease. The earliest phase of Alzheimer's disease (cellular phase) happens in parallel with accumulating amyloid beta, inducing the spread of tau pathology. The risk of Alzheimer's disease is 60-80% dependent on heritable factors, with more than 40 Alzheimer's disease-associated genetic risk loci already identified, of which the APOE alleles have the strongest association with the disease. Novel biomarkers include PET scans and plasma assays for amyloid beta and phosphorylated tau, which show great promise for clinical and research use. Multidomain lifestyle-based prevention trials suggest cognitive benefits in participants with increased risk of dementia. Lifestyle factors do not directly affect Alzheimer's disease pathology, but can still contribute to a positive outcome in individuals with Alzheimer's disease. Promising pharmacological treatments are poised at advanced stages of clinical trials and include anti-amyloid beta, anti-tau, and anti-inflammatory strategies.
机译:在本次研讨会上,我们将重点介绍阿尔茨海默病领域的主要进展。最新数据表明,到2050年,欧洲痴呆症的患病率将翻一番,全世界痴呆症的患病率将翻三番,而根据阿尔茨海默病的生物学(而非临床)定义,这一估计将高出三倍。阿尔茨海默病的最早阶段(细胞期)与积累β淀粉样蛋白同时发生,导致tau病理学的传播。阿尔茨海默病的风险60-80%取决于遗传因素,已经确定了40多个与阿尔茨海默病相关的遗传风险位点,其中APOE等位基因与该病的相关性最强。新的生物标记物包括PET扫描和淀粉样β和磷酸化tau的血浆分析,这在临床和研究中显示了巨大的应用前景。基于生活方式的多领域预防试验表明,痴呆症风险增加的参与者认知能力增强。生活方式因素不会直接影响阿尔茨海默病的病理学,但仍有助于阿尔茨海默病患者的积极结果。有希望的药物治疗处于临床试验的晚期阶段,包括抗淀粉样β、抗tau和抗炎策略。

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