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阿尔茨海默病:从淀粉样肽和氧化应激到生物标志物技术和疾病预防策略的探索——来自 AIBL 和 DIAN 队列研究的收获。

Alzheimer's Disease: A Journey from Amyloid Peptides and Oxidative Stress, to Biomarker Technologies and Disease Prevention Strategies-Gains from AIBL and DIAN Cohort Studies.

机构信息

Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.

Australian Alzheimer's Research Foundation, Ralph and Patricia Sarich Neuroscience Research Institute, Nedlands, WA, Australia.

出版信息

J Alzheimers Dis. 2018;62(3):965-992. doi: 10.3233/JAD-171145.

Abstract

Worldwide there are over 46 million people living with dementia, and this number is expected to double every 20 years reaching about 131 million by 2050. The cost to the community and government health systems, as well as the stress on families and carers is incalculable. Over three decades of research into this disease have been undertaken by several research groups in Australia, including work by our original research group in Western Australia which was involved in the discovery and sequencing of the amyloid-β peptide (also known as Aβ or A4 peptide) extracted from cerebral amyloid plaques. This review discusses the journey from the discovery of the Aβ peptide in Alzheimer's disease (AD) brain to the establishment of pre-clinical AD using PET amyloid tracers, a method now serving as the gold standard for developing peripheral diagnostic approaches in the blood and the eye. The latter developments for early diagnosis have been largely achieved through the establishment of the Australian Imaging Biomarker and Lifestyle research group that has followed 1,100 Australians for 11 years. AIBL has also been instrumental in providing insight into the role of the major genetic risk factor apolipoprotein E ɛ4, as well as better understanding the role of lifestyle factors particularly diet, physical activity and sleep to cognitive decline and the accumulation of cerebral Aβ.

摘要

全球有超过 4600 万人患有痴呆症,预计这个数字每 20 年就会翻一番,到 2050 年将达到约 1.31 亿。这给社区和政府卫生系统带来的成本,以及给家庭和护理人员带来的压力是无法估量的。三十多年来,澳大利亚的几个研究小组一直在研究这种疾病,包括我们在西澳大利亚的最初研究小组,该小组参与了从大脑淀粉样斑块中提取的淀粉样β肽(也称为 Aβ或 A4 肽)的发现和测序。这篇综述讨论了从阿尔茨海默病(AD)大脑中 Aβ肽的发现到使用 PET 淀粉样蛋白示踪剂建立临床前 AD 的历程,这种方法现在是开发血液和眼睛外周诊断方法的金标准。通过建立澳大利亚成像生物标志物和生活方式研究小组,对早期诊断的进一步发展已经取得了很大进展,该小组对 1100 名澳大利亚人进行了 11 年的跟踪研究。AIBL 还为了解载脂蛋白 Eɛ4 这一主要遗传风险因素的作用以及更好地理解饮食、体育活动和睡眠等生活方式因素对认知能力下降和大脑 Aβ积累的作用提供了重要的见解。

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