Practical detection of a definitive biomarker panel for Alzheimer's disease; comparisons between matched plasma and cerebrospinal fluid

被引:0
作者
Richens, Joanna L. [1 ]
Vere, Kelly-Ann [1 ]
Light, Roger A. [2 ]
Soria, Daniele [3 ,4 ]
Garibaldi, Jonathan [3 ,4 ]
Smith, A. David [5 ]
Warden, Donald [5 ]
Wilcock, Gordon [6 ]
Bajaj, Nin [7 ]
Morgan, Kevin [8 ]
O'Shea, Paul [1 ]
机构
[1] Univ Nottingham, Sch Life Sci, Inst Biophys Imaging & Optic Sci, Cell Biophys Grp, Nottingham NG7 2RD, England
[2] Univ Nottingham, Inst Biophys Imaging & Optic Sci, Nottingham, England
[3] Univ Nottingham, Sch Comp Sci, Jubilee Campus, Nottingham, England
[4] Univ Nottingham, Adv Data Anal Ctr, Nottingham, England
[5] Univ Oxford, Univ Dept Physiol Anat & Genet, OPTIMA, Oxford, England
[6] John Radcliffe Hosp, Nuffield Dept Clin Med, Oxford Project Invest Memory & Ageing, Oxford, England
[7] Nottingham Univ Hosp NHS Trust, Queens Med Ctr, Dept Neurol, Nottingham, England
[8] Univ Nottingham, Queens Med Ctr, Sch Life Sci, Translat Cell Sci Human Genet Grp, Nottingham, England
来源
INTERNATIONAL JOURNAL OF MOLECULAR EPIDEMIOLOGY AND GENETICS | 2014年 / 5卷 / 02期
基金
英国医学研究理事会;
关键词
Alzheimer's disease; biomarker; blood plasma; cerebrospinal fluid;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Previous mass spectrometry analysis of cerebrospinal fluid (CSF) has allowed the identification of a panel of molecular markers that are associated with Alzheimer's disease (AD). The panel comprises Amyloid beta, Apolipoprotein E, Fibrinogen alpha chain precursor, Keratin type I cytoskeletal 9, Serum albumin precursor, SPARC-like 1 protein and Tetranectin. Here we report the development and implementation of immunoassays to measure the abundance and diagnostic capacity of these putative biomarkers in matched lumbar CSF and blood plasma samples taken in life from individuals confirmed at post-mortem as suffering from AD (n = 10) and from screened 'cognitively healthy' subjects (n = 18). The inflammatory components of Alzheimer's disease were also investigated. Employment of supervised learning techniques permitted examination of the interrelated expression patterns of the putative biomarkers and identified inflammatory components, resulting in biomarker panels with a diagnostic accuracy of 87.5% and 86.7% for the plasma and CSF datasets respectively. This is extremely important as it offers an ideal high-throughput and relatively inexpensive population screening approach. It appears possible to determine the presence or absence of AD based on our biomarker panel and it seems likely that a cheap and rapid blood test for AD is feasible.
引用
收藏
页码:53 / 70
页数:18
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