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痴呆症预防研究诊所:一项在新西兰奥特亚罗瓦进行的纵向研究,调查影响阿尔茨海默病发病的因素。

Dementia Prevention Research Clinic: a longitudinal study investigating factors influencing the development of Alzheimer's disease in Aotearoa, New Zealand.

作者信息

Tippett Lynette J, Cawston Erin E, Morgan Catherine A, Melzer Tracy R, Brickell Kiri L, Ilse Christina, Cheung Gary, Kirk Ian J, Roberts Reece P, Govender Jane, Griner Leon, Le Heron Campbell, Buchanan Sarah, Port Waiora, Dudley Makarena, Anderson Tim J, Williams Joanna M, Cutfield Nicholas J, Dalrymple-Alford John C, Wood Phil

机构信息

NZ-Dementia Prevention Research Clinic, New Zealand.

School of Psychology, University of Auckland, Auckland, New Zealand.

出版信息

J R Soc N Z. 2022 Aug 24;53(4):489-510. doi: 10.1080/03036758.2022.2098780. eCollection 2023.

DOI:10.1080/03036758.2022.2098780
PMID:39439970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11459802/
Abstract

Aotearoa New Zealand's population is ageing. Increasing life expectancy is accompanied by increases in prevalence of Alzheimer's Disease (AD) and ageing-related disorders. The multicentre Dementia Prevention Research Clinic longitudinal study aims to improve understanding of AD and dementia in Aotearoa, in order to develop interventions that delay or prevent progression to dementia. Comprising research clinics in Auckland, Christchurch and Dunedin, this multi-disciplinary study involves community participants who undergo biennial investigations informed by international protocols and best practice: clinical, neuropsychological, neuroimaging, lifestyle evaluations, genotyping, blood collection and processing. A key research objective is to identify a 'biomarker signature' that predicts progression from mild cognitive impairment to AD. Candidate biomarkers include: blood proteins and microRNAs, genetic, neuroimaging and neuropsychological markers, health, cultural, lifestyle, sensory and psychosocial factors. We are examining a range of mechanisms underlying the progression of AD pathology (e.g. faulty blood-brain barrier, excess parenchymal iron, vascular dysregulation). This paper will outline key aspects of the Dementia Prevention Research Clinic's research, provide an overview of data collection, and a summary of 266 participants recruited to date. The national outreach of the clinics is a strength; the heart of the Dementia Prevention Research Clinics are its people.

摘要

新西兰的人口正在老龄化。预期寿命的增加伴随着阿尔茨海默病(AD)和与衰老相关疾病患病率的上升。多中心痴呆预防研究诊所纵向研究旨在增进对新西兰AD和痴呆症的了解,以便制定干预措施来延缓或预防痴呆症的进展。这项多学科研究包括奥克兰、克赖斯特彻奇和达尼丁的研究诊所,涉及社区参与者,他们按照国际协议和最佳实践每两年接受一次调查:临床、神经心理学、神经影像学、生活方式评估、基因分型、血液采集和处理。一个关键的研究目标是确定一个能预测从轻度认知障碍进展为AD的“生物标志物特征”。候选生物标志物包括:血液蛋白质和微小RNA、遗传、神经影像学和神经心理学标志物、健康、文化、生活方式、感官和社会心理因素。我们正在研究AD病理进展背后的一系列机制(例如血脑屏障功能障碍、实质铁过量、血管调节异常)。本文将概述痴呆预防研究诊所研究的关键方面,提供数据收集概述,并总结迄今为止招募的266名参与者的情况。诊所的全国性推广是一项优势;痴呆预防研究诊所的核心是其工作人员。

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本文引用的文献

1
Reproducibility and repeatability of magnetic resonance imaging in dementia.磁共振成像在痴呆症中的可重复性和再现性。
Phys Med. 2022 Sep;101:8-17. doi: 10.1016/j.ejmp.2022.06.012. Epub 2022 Jul 16.
2
Screening and enrollment of underrepresented ethnocultural and educational populations in the Alzheimer's Disease Neuroimaging Initiative (ADNI).在阿尔茨海默病神经影像学倡议(ADNI)中对代表性不足的族裔文化和教育人群进行筛查和招募。
Alzheimers Dement. 2022 Dec;18(12):2603-2613. doi: 10.1002/alz.12640. Epub 2022 Feb 25.
3
Plasma microRNA vary in association with the progression of Alzheimer's disease.血浆微小RNA随阿尔茨海默病的进展而变化。
Alzheimers Dement (Amst). 2022 Feb 5;14(1):e12251. doi: 10.1002/dad2.12251. eCollection 2022.
4
Spatial variation of perfusion MRI reflects cognitive decline in mild cognitive impairment and early dementia.灌注 MRI 的空间变异性反映了轻度认知障碍和早期痴呆患者认知能力的下降。
Sci Rep. 2021 Dec 2;11(1):23325. doi: 10.1038/s41598-021-02313-z.
5
Arterial Stiffening Moderates the Relationship Between Type-2 Diabetes Mellitus and White Matter Hyperintensity Burden in Older Adults With Mild Cognitive Impairment.动脉僵硬度调节轻度认知障碍老年人2型糖尿病与白质高信号负荷之间的关系。
Front Aging Neurosci. 2021 Oct 25;13:716638. doi: 10.3389/fnagi.2021.716638. eCollection 2021.
6
Diversity in Alzheimer's disease drug trials: The importance of eligibility criteria.阿尔茨海默病药物试验中的多样性:入选标准的重要性。
Alzheimers Dement. 2022 Apr;18(4):810-823. doi: 10.1002/alz.12433. Epub 2021 Sep 30.
7
Differences in the potential for dementia prevention between major ethnic groups within one country: A cross sectional analysis of population attributable fraction of potentially modifiable risk factors in New Zealand.一个国家内主要种族群体在预防痴呆症方面的潜力差异:新西兰潜在可改变风险因素的人群归因分数的横断面分析。
Lancet Reg Health West Pac. 2021 Jul 5;13:100191. doi: 10.1016/j.lanwpc.2021.100191. eCollection 2021 Aug.
8
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.阿尔茨海默病的常见变异与多基因风险评分的风险分层。
Nat Commun. 2021 Jun 7;12(1):3417. doi: 10.1038/s41467-021-22491-8.
9
The PrecivityAD™ test: Accurate and reliable LC-MS/MS assays for quantifying plasma amyloid beta 40 and 42 and apolipoprotein E proteotype for the assessment of brain amyloidosis.PrecivityAD™ 测试:用于定量检测血浆淀粉样蛋白β 40 和 42 以及载脂蛋白 E 蛋白型的准确可靠的 LC-MS/MS 分析方法,用于评估脑淀粉样变性。
Clin Chim Acta. 2021 Aug;519:267-275. doi: 10.1016/j.cca.2021.05.011. Epub 2021 May 17.
10
Associations of Alzheimer's disease risk variants with gene expression, amyloidosis, tauopathy, and neurodegeneration.阿尔茨海默病风险变异与基因表达、淀粉样变性、tau 病和神经退行性变的关联。
Alzheimers Res Ther. 2021 Jan 8;13(1):15. doi: 10.1186/s13195-020-00755-7.