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本文引用的文献

1
Variability of CSF Alzheimer's disease biomarkers: implications for clinical practice.脑脊液中阿尔茨海默病生物标志物的变异性:对临床实践的影响。
PLoS One. 2014 Jun 24;9(6):e100784. doi: 10.1371/journal.pone.0100784. eCollection 2014.
2
Biobanking of CSF: international standardization to optimize biomarker development.CSF 生物样本库:国际标准化以优化生物标志物的开发。
Clin Biochem. 2014 Mar;47(4-5):288-92. doi: 10.1016/j.clinbiochem.2013.12.024. Epub 2014 Jan 2.
3
Recommendations to standardize preanalytical confounding factors in Alzheimer's and Parkinson's disease cerebrospinal fluid biomarkers: an update.推荐标准化阿尔茨海默病和帕金森病脑脊液生物标志物的分析前混杂因素:更新。
Biomark Med. 2012 Aug;6(4):419-30. doi: 10.2217/bmm.12.46.
4
Reference measurement procedures for Alzheimer's disease cerebrospinal fluid biomarkers: definitions and approaches with focus on amyloid β42.阿尔茨海默病脑脊液生物标志物的参考测量程序:重点是β淀粉样蛋白 42 的定义和方法。
Biomark Med. 2012 Aug;6(4):409-17. doi: 10.2217/bmm.12.39.
5
The Alzheimer's Association external quality control program for cerebrospinal fluid biomarkers.阿尔茨海默病协会脑脊液生物标志物外部质量控制计划。
Alzheimers Dement. 2011 Jul;7(4):386-395.e6. doi: 10.1016/j.jalz.2011.05.2243.
6
α-Synuclein and tau concentrations in cerebrospinal fluid of patients presenting with parkinsonism: a cohort study.帕金森病患者脑脊液中α-突触核蛋白和tau 浓度:一项队列研究。
Lancet Neurol. 2011 Mar;10(3):230-40. doi: 10.1016/S1474-4422(11)70014-X.
7
Quantification of α-synuclein in cerebrospinal fluid as a biomarker candidate: review of the literature and considerations for future studies.脑脊液中α-突触核蛋白的定量作为生物标志物候选物:文献回顾及对未来研究的考虑。
Biomark Med. 2010 Oct;4(5):683-99. doi: 10.2217/bmm.10.90.
8
Standardization of Assay Procedures for Analysis of the CSF Biomarkers Amyloid β((1-42)), Tau, and Phosphorylated Tau in Alzheimer's Disease: Report of an International Workshop.阿尔茨海默病脑脊液生物标志物淀粉样β(1-42)、tau蛋白和磷酸化tau蛋白分析检测程序的标准化:国际研讨会报告
Int J Alzheimers Dis. 2010 Sep 27;2010:635053. doi: 10.4061/2010/635053.
9
Confounding factors influencing amyloid Beta concentration in cerebrospinal fluid.影响脑脊液中β淀粉样蛋白浓度的混杂因素。
Int J Alzheimers Dis. 2010 Jul 15;2010:986310. doi: 10.4061/2010/986310.
10
Cerebrospinal fluid and plasma biomarkers in Alzheimer disease.阿尔茨海默病的脑脊液和血浆生物标志物。
Nat Rev Neurol. 2010 Mar;6(3):131-44. doi: 10.1038/nrneurol.2010.4. Epub 2010 Feb 16.

BIOMARKAPD的中央生物样本库和虚拟生物样本库:神经退行性疾病研究资源

The Central Biobank and Virtual Biobank of BIOMARKAPD: A Resource for Studies on Neurodegenerative Diseases.

作者信息

Reijs Babette L R, Teunissen Charlotte E, Goncharenko Nikolai, Betsou Fay, Blennow Kaj, Baldeiras Inês, Brosseron Frederic, Cavedo Enrica, Fladby Tormod, Froelich Lutz, Gabryelewicz Tomasz, Gurvit Hakan, Kapaki Elisabeth, Koson Peter, Kulic Luka, Lehmann Sylvain, Lewczuk Piotr, Lleó Alberto, Maetzler Walter, de Mendonça Alexandre, Miller Anne-Marie, Molinuevo José L, Mollenhauer Brit, Parnetti Lucilla, Rot Uros, Schneider Anja, Simonsen Anja Hviid, Tagliavini Fabrizio, Tsolaki Magda, Verbeek Marcel M, Verhey Frans R J, Zboch Marzena, Winblad Bengt, Scheltens Philip, Zetterberg Henrik, Visser Pieter Jelle

机构信息

Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Alzheimer Center Limburg, Maastricht University Medical Center , Maastricht , Netherlands.

Neurochemistry Laboratory and Biobank, Department of Clinical Chemistry, VU University Medical Center , Amsterdam , Netherlands.

出版信息

Front Neurol. 2015 Oct 15;6:216. doi: 10.3389/fneur.2015.00216. eCollection 2015.

DOI:10.3389/fneur.2015.00216
PMID:26528237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4606063/
Abstract

Biobanks are important resources for biomarker discovery and assay development. Biomarkers for Alzheimer's and Parkinson's disease (BIOMARKAPD) is a European multicenter study, funded by the EU Joint Programme-Neurodegenerative Disease Research, which aims to improve the clinical use of body fluid markers for the diagnosis and prognosis of Alzheimer's disease (AD) and Parkinson's disease (PD). The objective was to standardize the assessment of existing assays and to validate novel fluid biomarkers for AD and PD. To support the validation of novel biomarkers and assays, a central and a virtual biobank for body fluids and associated data from subjects with neurodegenerative diseases have been established. In the central biobank, cerebrospinal fluid (CSF) and blood samples were collected according to the BIOMARKAPD standardized pre-analytical procedures and stored at Integrated BioBank of Luxembourg. The virtual biobank provides an overview of available CSF, plasma, serum, and DNA samples at each site. Currently, at the central biobank of BIOMARKAPD samples are available from over 400 subjects with normal cognition, mild cognitive impairment (MCI), AD, frontotemporal dementia (FTD), vascular dementia, multiple system atrophy, progressive supranuclear palsy, PD, PD with dementia, and dementia with Lewy bodies. The virtual biobank contains information on over 8,600 subjects with varying diagnoses from 21 local biobanks. A website has been launched to enable sample requests from the central biobank and virtual biobank.

摘要

生物样本库是生物标志物发现和检测方法开发的重要资源。阿尔茨海默病和帕金森病生物标志物(BIOMARKAPD)是一项欧洲多中心研究,由欧盟联合计划——神经退行性疾病研究资助,旨在改善体液标志物在阿尔茨海默病(AD)和帕金森病(PD)诊断及预后方面的临床应用。其目标是规范现有检测方法的评估,并验证用于AD和PD的新型体液生物标志物。为支持新型生物标志物和检测方法的验证,已建立了一个针对神经退行性疾病患者的体液及相关数据的中央生物样本库和一个虚拟生物样本库。在中央生物样本库中,脑脊液(CSF)和血液样本按照BIOMARKAPD标准化的分析前程序收集,并存储于卢森堡综合生物样本库。虚拟生物样本库提供了每个站点可用的CSF、血浆、血清和DNA样本的概述。目前,在BIOMARKAPD的中央生物样本库中,有来自400多名认知正常、轻度认知障碍(MCI)、AD、额颞叶痴呆(FTD)、血管性痴呆、多系统萎缩、进行性核上性麻痹、PD伴痴呆、路易体痴呆患者的样本。虚拟生物样本库包含来自21个地方生物样本库的8600多名诊断各异的受试者的信息。已推出一个网站,以便从中央生物样本库和虚拟生物样本库请求样本。