Galvin James E
Comprehensive Center for Brain Health, Department of Integrated Medical Sciences, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, Florida.
J Am Geriatr Soc. 2017 Oct;65(10):2128-2133. doi: 10.1111/jgs.14997. Epub 2017 Aug 2.
Alzheimer's disease (AD) affects more than 5 million Americans, with substantial consequences for individuals with AD, families, and society in terms of morbidity, mortality, and healthcare costs. With disease-modifying treatment trials unsuccessful at the present time and only medications to treat symptoms available, an emerging approach is prevention. Advances in diagnostic criteria, biomarker development, and greater understanding of the biophysiological basis of AD make these initiatives feasible. Ongoing pharmacological trials using anti-amyloid therapies are underway in sporadic and genetic forms of AD, although a large number of modifiable risk factors for AD have been identified in observational studies, many of which do not appear to exert effects through amyloid or tau. This suggests that prevention studies focusing on risk reduction and lifestyle modification may offer additional benefits. Rather than relying solely on large-sample, long-duration, randomized clinical trial designs, a precision medicine approach using N-of-1 trials may provide more-rapid information on whether personalized prevention plans can improve person-centered outcomes. Because there appear to be multiple pathways to developing AD, there may also be multiple ways to prevent or delay the onset of AD. Even if these precision approaches alone are not successful in preventing AD, they may greatly improve the likelihood of amyloid- or tau-specific therapies to reach their endpoints by reducing comorbidities. Keeping this in mind, dementia may be a disorder that develops over a lifetime, with individualized ways to build a better brain as we age.
阿尔茨海默病(AD)影响着超过500万美国人,在发病率、死亡率和医疗成本方面给AD患者、家庭及社会带来了重大影响。鉴于目前疾病修饰治疗试验未获成功,且仅有对症治疗药物可用,一种新出现的方法是预防。诊断标准的进步、生物标志物的开发以及对AD生物生理基础的更深入了解使这些举措切实可行。目前正在针对散发性和遗传性AD开展使用抗淀粉样蛋白疗法的药理学试验,尽管在观察性研究中已确定了大量可改变的AD风险因素,但其中许多因素似乎并非通过淀粉样蛋白或tau发挥作用。这表明专注于降低风险和改变生活方式的预防研究可能会带来额外益处。使用单病例试验的精准医学方法可能会比单纯依赖大样本、长期的随机临床试验设计更快地提供有关个性化预防计划是否能改善以患者为中心的结局的信息。由于AD的发病似乎存在多种途径,预防或延缓AD发病可能也有多种方法。即使这些精准方法本身无法成功预防AD,它们也可能通过减少合并症大大提高淀粉样蛋白或tau特异性疗法达到其终点的可能性。牢记这一点,痴呆症可能是一种伴随一生发展的疾病,随着年龄增长,有个性化的方法来打造更健康的大脑。