Quantification of total apolipoprotein E and its specific isoforms in cerebrospinal fluid and blood in Alzheimer’s disease and other neurodegenerative diseases

Q4 Biochemistry, Genetics and Molecular Biology EuPA Open Proteomics Pub Date : 2015-09-01 DOI:10.1016/j.euprot.2015.07.012
Melinda Rezeli , Henrik Zetterberg , Kaj Blennow , Ann Brinkmalm , Thomas Laurell , Oskar Hansson , György Marko-Varga
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引用次数: 36

Abstract

A targeted mass spectrometric assay was developed for identification and quantification of apoE isoforms (apoE2, E3 and E4), and it was utilized for screening of samples from AD patients (n = 39) and patients with other neurodegenerative disorders (n = 38). The assay showed good linearity with LOQ corresponds to total apoE concentration of 0.8 and 40 ng/mL in CSF and plasma/serum, respectively. We identified apoE phenotypes with 100% accuracy in clinical samples. We found strong association between genotypes of the individuals and their apoE levels in blood; ϵ4 allele carriers had significantly lower apoE levels in blood than non-carriers.

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阿尔茨海默病和其他神经退行性疾病患者脑脊液和血液中总载脂蛋白E及其特异性亚型的定量分析
建立了一种靶向质谱分析方法,用于鉴定和定量apoE亚型(apoE2, E3和E4),并将其用于筛选AD患者(n = 39)和其他神经退行性疾病患者(n = 38)的样本。检测结果线性良好,定量限对应于脑脊液和血浆/血清中总载脂蛋白e浓度分别为0.8和40 ng/mL。我们在临床样本中以100%的准确率确定了载脂蛋白e表型。我们发现个体的基因型与其血液中载脂蛋白e水平有很强的相关性;ϵ4等位基因携带者血液中载脂蛋白e水平明显低于非携带者。
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EuPA Open Proteomics
EuPA Open Proteomics Biochemistry, Genetics and Molecular Biology-Biochemistry
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Proceedings of the EuBIC-MS 2020 Developers’ Meeting Editorial: The next generation in (EuPA Open) Proteomics Aims & scope Proceedings of the EuBIC Winter School 2019 Introducing the YPIC challenge
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